55 results on '"Inoue, Kimiko"'
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2. Noncanonical imprinting sustains embryonic development and restrains placental overgrowth
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Matoba, Shogo, Kozuka, Chisayo, Miura, Kento, Inoue, Kimiko, Kumon, Mami, Hayashi, Ryoya, Ohhata, Tatsuya, Ogura, Atsuo, and Inoue, Azusa
- Abstract
In this study, Matoba et al. use a combinatorial maternal KO of Xist, a noncanonical imprinted gene whose LOI causes aberrant transient maternal X-chromosome inactivation (XCI) at preimplantation, and show that prevention of the transient maternal XCI greatly restores the development of EedmatKO embryos. Their findings provide evidence that Xistimprinting sustains embryonic development and that autosomal noncanonical imprinting restrains placental overgrowth.
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- 2022
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3. Improved development of mouse somatic cell nuclear transfer embryos by chlamydocin analogues, class I and IIa histone deacetylase inhibitors†.
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Kamimura, Satoshi, Inoue, Kimiko, Mizutani, Eiji, Kim, Jin-Moon, Inoue, Hiroki, Ogonuki, Narumi, Miyamoto, Kei, Ihashi, Shunya, Itami, Nobuhiko, Wakayama, Teruhiko, Ito, Akihiro, Nishino, Norikazu, Yoshida, Minoru, and Ogura, Atsuo
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In mammalian cloning by somatic cell nuclear transfer (SCNT), the treatment of reconstructed embryos with histone deacetylase (HDAC) inhibitors improves efficiency. So far, most of those used for SCNT are hydroxamic acid derivatives-such as trichostatin A-characterized by their broad inhibitory spectrum. Here, we examined whether mouse SCNT efficiency could be improved using chlamydocin analogues, a family of newly designed agents that specifically inhibit class I and IIa HDACs. Development of SCNT-derived embryos in vitro and in vivo revealed that four out of five chlamydocin analogues tested could promote the development of cloned embryos. The highest pup rates (7.1-7.2%) were obtained with Ky-9, similar to those achieved with trichostatin A (7.2-7.3%). Thus, inhibition of class I and/or IIa HDACs in SCNT-derived embryos is enough for significant improvements in full-term development. In mouse SCNT, the exposure of reconstructed oocytes to HDAC inhibitors is limited to 8-10 h because longer inhibition with class I inhibitors causes a two-cell developmental block. Therefore, we used Ky-29, with higher selectivity for class IIa than class I HDACs for longer treatment of SCNT-derived embryos. As expected, 24-h treatment with Ky-29 up to the two-cell stage did not induce a developmental block, but the pup rate was not improved. This suggests that the one-cell stage is a critical period for improving SCNT cloning using HDAC inhibitors. Thus, chlamydocin analogues appear promising for understanding and improving the epigenetic status of mammalian SCNT-derived embryos through their specific inhibitory effects on HDACs.
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- 2021
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4. Development of assisted reproductive technologies for Mus spretus†
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Hasegawa, Ayumi, Mochida, Keiji, Matoba, Shogo, Inoue, Kimiko, Hama, Daiki, Kadota, Masayo, Hiraiwa, Noriko, Yoshiki, Atsushi, and Ogura, Atsuo
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The genus Musconsists of many species with high genetic diversity. However, only one species, Mus musculus(the laboratory mouse), is common in biomedical research. The unavailability of assisted reproductive technologies (ARTs) for other Musspecies might be a major reason for their limited use in laboratories. Here, we devised ARTs for Mus spretus(the Algerian mouse), a commonly used wild-derived Musspecies. We found that in vitro production of M. spretusembryos was difficult because of low efficacies of superovulation with equine chorionic gonadotropin or anti-inhibin serum (AIS) (5–8 oocytes per female) and a low fertilization rate following in vitro fertilization (IVF; 15.2%). The primary cause of this was the hardening of the zona pellucida but not the sperm’s fertilizing ability, as revealed by reciprocal IVF with laboratory mice. The largest number of embryos (16 per female) were obtained when females were injected with AIS followed by human chorionic gonadotropin and estradiol injections 24 h later, and then by natural mating. These in vivo-derived 2-cell embryos could be vitrified/warmed with a high survival rate (94%) using an ethylene glycol-based solution. Importantly, more than 60% of such embryos developed into healthy offspring following interspecific embryo transfer into (C57BL/6 × C3H) F1 female mice. Thus, we have devised practical ARTs for Mus spretusmice, enabling efficient production of embryos and animals, with safe laboratory preservation of their strains. In addition, we have demonstrated that interspecific embryo transfer is possible in murine rodents.Embryos from wild-derived Mus spretusmice can be efficiently produced, cryopreserved, and transferred into laboratory mouse females using newly developed assisted reproductive technology protocols.
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- 2021
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5. Reprogramming of the histone H3.3 landscape in the early mouse embryo
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Ishiuchi, Takashi, Abe, Shusaku, Inoue, Kimiko, Yeung, Wan Kin Au, Miki, Yuka, Ogura, Atsuo, and Sasaki, Hiroyuki
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Epigenetic reprogramming of the zygote involves dynamic incorporation of histone variant H3.3. However, the genome-wide distribution and dynamics of H3.3 during early development remain unknown. Here, we delineate the H3.3 landscapes in mouse oocytes and early embryos. We unexpectedly identify a non-canonical H3.3 pattern in mature oocytes and zygotes, in which local enrichment of H3.3 at active chromatin is suppressed and H3.3 is relatively evenly distributed across the genome. Interestingly, although the non-canonical H3.3 pattern forms gradually during oogenesis, it quickly switches to a canonical pattern at the two-cell stage in a transcription-independent and replication-dependent manner. We find that incorporation of H3.1/H3.2 mediated by chromatin assembly factor CAF-1 is a key process for the de novo establishment of the canonical pattern. Our data suggest that the presence of the non-canonical pattern and its timely transition toward a canonical pattern support the developmental program of early embryos.
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- 2021
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6. Pathological Findings in Male Patients With Anti-N-methyl-d-Aspartate Receptor Encephalitis
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Hirano, Makito, Itoh, Tatsuki, Fujimura, Harutoshi, Inoue, Kimiko, Samukawa, Makoto, Nose, Kazuhiro, Sakamoto, Hikaru, Maekura, Shunji, Ueno, Shuichi, Satou, Takao, Nishioka, Tsukasa, Kusunoki, Susumu, and Nakamura, Yusaku
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Anti-N-methyl-d-aspartate receptor (anti-NMDAR) encephalitis is the most common type of autoimmune encephalitis. The disease predominantly affects women (1:5–1:10), with only 3 reports of autopsy findings in women being published to date. The present study reports findings from the first autopsy performed on a man with anti-NMDAR encephalitis. The patient had some scattered lesions in the limbic system with neuronal loss, gliosis, and microglial activation. The temporal and frontal cortices showed additional patchy demyelination. T-lymphocyte infiltration was detectable in the fusiform gyrus lesion. These findings were partly similar to those reported in female patients. Although clinical differences based on the sex of the patient are reported for this disease, the observed pathological similarities potentially help to establish common therapeutic strategies for all patients. Severe testicular damage was additionally observed in the male patient in this study. Biopsy-proven severe testicular damage was also confirmed in another, previously fertile man who became azoospermic. Moreover, serum follicle-stimulating hormone levels, which often increased in response to disturbed spermatogenesis, were elevated, and testosterone/luteinizing hormone ratio reflecting Leydig cell function was low in all 5 male patients in this study. Overall, these findings suggest similar brain pathology in patients of both sexes and severe testicular damage in male patients.
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- 2019
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7. Aberrant imprinting in mouse trophoblast stem cells established from somatic cell nuclear transfer-derived embryos
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Hirose, Michiko, Hada, Masashi, Kamimura, Satoshi, Matoba, Shogo, Honda, Arata, Motomura, Kaori, Ogonuki, Narumi, Shawki, Hossam H., Inoue, Kimiko, Takahashi, Satoru, and Ogura, Atsuo
- Abstract
ABSTRACTAlthough phenotypic abnormalities frequently appear in the placenta following somatic cell nuclear transfer (SCNT), mouse trophoblast stem cells (TSCs) established from SCNT embryos reportedly show no distinct abnormalities compared with those derived from normal fertilization. In this study, we reexamined SCNT–TSCs to identify their imprinting statuses. Placenta-specific maternally imprinted genes (Gab1, Slc38a4, and Sfmbt2) consistently showed biallelic expression in SCNT–TSCs, suggesting their loss of imprinting (LOI). The LOI of Gab1was associated with decreased DNA methylation, and that of Sfmbt2was associated with decreased DNA methylation and histone H3K27 trimethylation. The maternal allele of the intergenic differentially methylated region (IG–DMR) was aberrantly hypermethylated following SCNT, even though this region was prone to demethylation in TSCs when established in a serum-free chemically defined medium. These findings indicate that the development of cloned embryos is associated with imprinting abnormalities specifically in the trophoblast lineage from its initial stage, which may affect subsequent placental development.
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- 2018
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8. Histone H3 Methylated at Arginine 17 Is Essential for Reprogramming the Paternal Genome in Zygotes
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Hatanaka, Yuki, Tsusaka, Takeshi, Shimizu, Natsumi, Morita, Kohtaro, Suzuki, Takehiro, Machida, Shinichi, Satoh, Manabu, Honda, Arata, Hirose, Michiko, Kamimura, Satoshi, Ogonuki, Narumi, Nakamura, Toshinobu, Inoue, Kimiko, Hosoi, Yoshihiko, Dohmae, Naoshi, Nakano, Toru, Kurumizaka, Hitoshi, Matsumoto, Kazuya, Shinkai, Yoichi, and Ogura, Atsuo
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At fertilization, the paternal genome undergoes extensive reprogramming through protamine-histone exchange and active DNA demethylation, but only a few maternal factors have been defined in these processes. We identified maternal Mettl23 as a protein arginine methyltransferase (PRMT), which most likely catalyzes the asymmetric dimethylation of histone H3R17 (H3R17me2a), as indicated by in vitro assays and treatment with TBBD, an H3R17 PRMT inhibitor. Maternal histone H3.3, which is essential for paternal nucleosomal assembly, is unable to be incorporated into the male pronucleus when it lacks R17me2a. Mettl23 interacts with Tet3, a 5mC-oxidizing enzyme responsible for active DNA demethylation, by binding to another maternal factor, GSE (gonad-specific expression). Depletion of Mettl23 from oocytes resulted in impaired accumulation of GSE, Tet3, and 5hmC in the male pronucleus, suggesting that Mettl23 may recruit GSE-Tet3 to chromatin. Our findings establish H3R17me2a and its catalyzing enzyme Mettl23 as key regulators of paternal genome reprogramming.
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- 2017
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9. The Rodent-Specific MicroRNA Cluster within the Sfmbt2Gene Is Imprinted and Essential for Placental Development
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Inoue, Kimiko, Hirose, Michiko, Inoue, Hiroki, Hatanaka, Yuki, Honda, Arata, Hasegawa, Ayumi, Mochida, Keiji, and Ogura, Atsuo
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MicroRNAs (miRNAs) represent small noncoding RNAs that are involved in physiological and developmental processes by posttranscriptionally inhibiting gene expression. One of the largest miRNA clusters in mice is located in intron 10 of the Sfmbt2gene, containing 72 miRNA precursor sequences. In this study, we generated mice lacking the entire Sfmbt2miRNA cluster to elucidate its functions during development. The Sfmbt2miRNAs were expressed predominantly from the paternal allele in the placenta, as is the host Sfmbt2gene. Loss of the paternal allele resulted in severely impaired development of the placenta, especially the spongiotrophoblast layer, and frequent lethality or defects of fetuses. The predicted target sequences of the miRNAs and gene expression analysis defined at least nine putative target genes, which function as tumor suppressors or apoptosis inducers. Our study has provided experimental evidence for the indispensable roles of placental miRNAs in trophoblast proliferation and thus fetal development.
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- 2017
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10. Histone Variants Enriched in Oocytes Enhance Reprogramming to Induced Pluripotent Stem Cells
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Shinagawa, Toshie, Takagi, Tsuyoshi, Tsukamoto, Daisuke, Tomaru, Chinatsu, Huynh, Linh My, Sivaraman, Padavattan, Kumarevel, Thirumananseri, Inoue, Kimiko, Nakato, Ryuichiro, Katou, Yuki, Sado, Takashi, Takahashi, Satoru, Ogura, Atsuo, Shirahige, Katsuhiko, and Ishii, Shunsuke
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Expression of Oct3/4, Sox2, Klf4, and c-Myc (OSKM) can reprogram somatic cells into induced pluripotent stem cells (iPSCs). Somatic cell nuclear transfer (SCNT) can also be used for reprogramming, suggesting that factors present in oocytes could potentially augment OSKM-mediated induction of pluripotency. Here, we report that two histone variants, TH2A and TH2B, which are highly expressed in oocytes and contribute to activation of the paternal genome after fertilization, enhance OSKM-dependent generation of iPSCs and can induce reprogramming with Klf4 and Oct3/4 alone. TH2A and TH2B are enriched on the X chromosome during the reprogramming process, and their expression in somatic cells increases the DNase I sensitivity of chromatin. In addition, Xistdeficiency, which was reported to enhance SCNT reprogramming efficiency, stimulates iPSC generation using TH2A/TH2B in conjunction with OSKM, but not OSKM alone. Thus, TH2A/TH2B may enhance reprogramming by introducing processes that normally operate in zygotes and during SCNT.
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- 2014
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11. Understanding the X chromosome inactivation cycle in mice
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Oikawa, Mami, Inoue, Kimiko, Shiura, Hirosuke, Matoba, Shogo, Kamimura, Satoshi, Hirose, Michiko, Mekada, Kazuyuki, Yoshiki, Atsushi, Tanaka, Satoshi, Abe, Kuniya, Ishino, Fumitoshi, and Ogura, Atsuo
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During mouse development, imprinted X chromosome inactivation (XCI) is observed in preimplantation embryos and is inherited to the placental lineage, whereas random XCI is initiated in the embryonic proper. XistRNA, which triggers XCI, is expressed ectopically in cloned embryos produced by somatic cell nuclear transfer (SCNT). To understand these mechanisms, we undertook a large-scale nuclear transfer study using different donor cells throughout the life cycle. The Xistexpression patterns in the reconstructed embryos suggested that the nature of imprinted XCI is the maternal Xist-repressing imprint established at the last stage of oogenesis. Contrary to the prevailing model, this maternal imprint is erased in both the embryonic and extraembryonic lineages. The lack of the Xist-repressing imprint in the postimplantation somatic cells clearly explains how the SCNT embryos undergo ectopic Xistexpression. Our data provide a comprehensive view of the XCI cycle in mice, which is essential information for future investigations of XCI mechanisms.
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- 2014
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12. The Arf GAP SMAP2 is necessary for organized vesicle budding from the trans-Golgi network and subsequent acrosome formation in spermiogenesis
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Funaki, Tomo, Kon, Shunsuke, Tanabe, Kenji, Natsume, Waka, Sato, Sayaka, Shimizu, Tadafumi, Yoshida, Naomi, Wong, Won Fen, Ogura, Atsuo, Ogawa, Takehiko, Inoue, Kimiko, Ogonuki, Narumi, Miki, Hiromi, Mochida, Keiji, Endoh, Keisuke, Yomogida, Kentarou, Fukumoto, Manabu, Horai, Reiko, Iwakura, Yoichiro, Ito, Chizuru, Toshimori, Kiyotaka, Watanabe, Toshio, and Satake, Masanobu
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SMAP2 is an Arf GAP and modulates clathrin-coated vesicle formation. SMAP2-deficient male mice exhibited globozoospermia due to acrosome deformation. In SMAP2(−/−) spermatids, budding of proacrosomal vesicles from the TGN was distorted and clathrin traffic–related molecules such as CALM and syntaxin2 were mislocated.
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- 2013
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13. ROS Are Required for Mouse Spermatogonial Stem Cell Self-Renewal
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Morimoto, Hiroko, Iwata, Kazumi, Ogonuki, Narumi, Inoue, Kimiko, Atsuo, Ogura, Kanatsu-Shinohara, Mito, Morimoto, Takeshi, Yabe-Nishimura, Chihiro, and Shinohara, Takashi
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Reactive oxygen species (ROS) generation is implicated in stem cell self-renewal in several tissues but is thought to be detrimental for spermatogenesis as well as spermatogonial stem cells (SSCs). Using cultured SSCs, we show that ROS are generated via the AKT and MEK signaling pathways under conditions where the growth factors glial cell line-derived neurotrophic factor and fibroblast growth factor 2 drive SSC self-renewal and, instead, stimulate self-renewal at physiological levels. SSCs depleted of ROS stopped proliferating, but they showed enhanced self-renewal when ROS levels were increased by the addition of hydrogen peroxide, which induced the phosphorylation of stress kinases p38 mitogen-activated protein kinase (MAPK) and c-junN-terminal kinase (JNK). Moreover, ROS depletion in vivo decreased SSC number in the testis, and NADPH oxidase 1 (Nox1)-deficient SSCs exhibited reduced self-renewal division upon serial transplantation. These results suggest that ROS generated by Nox1 play critical roles in SSC self-renewal via the activation of the p38 MAPK and JNK pathways.
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- 2013
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14. Reconstitution of Mouse Spermatogonial Stem Cell Niches in Culture
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Kanatsu-Shinohara, Mito, Inoue, Kimiko, Takashima, Seiji, Takehashi, Masanori, Ogonuki, Narumi, Morimoto, Hiroko, Nagasawa, Takashi, Ogura, Atsuo, and Shinohara, Takashi
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Spermatogonial stem cells (SSCs) reside in specific niches within seminiferous tubules. These niches are thought to secrete chemotactic factors for SSCs, because SSCs migrate to them upon transplantation. However, the identity of these chemotactic molecules remains unknown. Here, we established a testis feeder cell culture system and used it to identify SSC chemotactic factors. When seeded on testis cells from infertile mice, SSCs migrated beneath the Sertoli cells and formed colonies with a cobblestone appearance that were very similar to those produced by hematopoietic stem cells. Cultured cells maintained SSC activity and fertility for at least 5 months. Cobblestone colony formation depended on GDNF and CXCL12, and dominant-negative GDNF receptor transfection or CXCL12 receptor deficiency reduced SSC colonization. Moreover, GDNF upregulated CXCL12 receptor expression, and CXCL12 transfection in Sertoli cells increased homing efficiency. Overall, our findings identify GDNF and CXCL12 as SSC chemotactic factors in vitro and in vivo.
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- 2012
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15. Production of Mouse Embryonic Stem Cell Lines from Maturing Oocytes by Direct Conversion of Meiosis into Mitosis
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Fulka, Helena, Hirose, Michiko, Inoue, Kimiko, Ogonuki, Narumi, Wakisaka, Noriko, Matoba, Shogo, Ogura, Atsuo, Mosko, Tibor, Kott, Tomas, and Fulka, Josef
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ESCs are most commonly derived from embryos originating from oocytes that reached metaphase II. We describe here a novel approach where ESCs with all pluripotency parameters were established from oocytes in which metaphase I was converted, from the cell cycle perspective, directly into metaphase II‐like stage without the intervening anaphase to telophase I transition. The resulting embryos initiate development and reach the blastocyst stage from which the ESC lines are then established. Thus, our approach could represent an ethically acceptable method that can exploit oocytes that are typically discarded in in vitro fertilization clinics. Moreover, our results also indicate that the meiotic cell cycle can be converted into mitosis by modulating chromosomal contacts that are typical for meiosis with subsequent licensing of chromatin for DNA replication. STEMCELLS2011;29:517–527
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- 2011
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16. Serum- and Feeder-Free Culture of Mouse Germline Stem Cells1
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Kanatsu-Shinohara, Mito, Inoue, Kimiko, Ogonuki, Narumi, Morimoto, Hiroko, Ogura, Atsuo, and Shinohara, Takashi
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Spermatogonial stem cells (SSCs) undergo self-renewal divisions to support spermatogenesis. Although several in vitro SSC culture systems have been developed, these systems include serum or fibroblast feeders, which complicate SSC self-renewal analyses. Here, we developed a serum- and feeder-free culture system for long-term propagation of SSCs. In addition to the SSC self-renewal factors, including glial cell line-derived neurotrophic factor, supplementation with fetuin and lipid-associated molecules was required to drive SSC proliferation in vitro. Cultured cells proliferated for at least 6 mo at a rate comparable to that of serum-supplemented cultured cells. However, germline potential was reduced under serum- and feeder-free conditions, as indicated by a lower SSC frequency after germ cell transplantation. Nevertheless, the cultured cells completed spermatogenesis and produced offspring following spermatogonial transplantation into seminiferous tubules of infertile mice. This culture system provides a basic platform for understanding the regulation of SSC fate commitment in vitro and for improving SSC culture medium.
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- 2011
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17. Heritable Imprinting Defect Caused by Epigenetic Abnormalities in Mouse Spermatogonial Stem Cells1
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Lee, Jiyoung, Kanatsu-Shinohara, Mito, Ogonuki, Narumi, Miki, Hiromi, Inoue, Kimiko, Morimoto, Takeshi, Morimoto, Hiroko, Ogura, Atsuo, and Shinohara, Takashi
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Male germ cells undergo dynamic epigenetic reprogramming during fetal development, eventually establishing spermatogonial stem cells (SSCs) that can convert into pluripotent stem cells. However, little is known about the developmental potential of fetal germ cells and how they mature into SSCs. We developed a culture system for fetal germ cells that proliferate for long periods of time. Male germ cells from embryos 12.5–18.5 days postcoitum could expand by glial cell line-derived neurotrophic factor, a self-renewal factor for SSCs. These cells did not form teratomas, but repopulated seminiferous tubules and produced spermatogenesis, exhibiting spermatogonia potential. However, the offspring from cultured cells showed growth abnormalities and were defective in genomic imprinting. The imprinting defect persisted in both the male and female germlines for at least four generations. Moreover, germ cells in the offspring showed abnormal histone modifications and DNA methylation patterns. These results indicate that fetal germ cells have a limited ability to become pluripotent cells and lose the ability to undergo epigenetic reprogramming by in vitro culture.
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- 2009
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18. Pluripotency of a Single Spermatogonial Stem Cell in Mice1
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Kanatsu-Shinohara, Mito, Lee, Jiyoung, Inoue, Kimiko, Ogonuki, Narumi, Miki, Hiromi, Toyokuni, Shinya, Ikawa, Masahito, Nakamura, Tomoyuki, Ogura, Atsuo, and Shinohara, Takashi
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Although pluripotent stem cells were recently discovered in postnatal testis, attempts to analyze their developmental potential have led to conflicting claims that spermatogonial stem cells are pluripotent or that they lose spermatogenic potential after conversion into pluripotent stem cells. To examine this issue, we analyzed the developmental fate of a single spermatogonial stem cell that appeared during transfection experiments. After transfection of a neomycin-resistance gene into germline stem cells, we obtained an embryonic stem-like, multipotent germline stem cell line. Southern blot analysis revealed that the germline stem and multipotent germline stem clones have the same transgene integration pattern, demonstrating their identical origin. The two lines, however, have different DNA methylation patterns. The multipotent germline stem cells formed chimeras after blastocyst injection but did not produce sperm after germ cell transplantation, whereas the germline stem cells could produce only spermatozoa and did not differentiate into somatic cells. Interestingly, the germline stem cells expressed several transcription factors (Pou5f1, Sox2, Myc, and Klf4) required for reprogramming fibroblasts into a pluripotent state, suggesting that they are potentially pluripotent. Thus, our study provides evidence that a single spermatogonial stem cell can acquire pluripotentiality but that conversion into a pluripotent cell type is accompanied by loss of spermatogenic potential.
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- 2008
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19. Dynamic Behavior of FCHO1 Revealed by Live-Cell Imaging Microscopy: Its Possible Involvement in Clathrin-Coated Vesicle Formation
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SAKAUSHI, Shinji, INOUE, Kimiko, ZUSHI, Hitomi, SENDA-MURATA, Kaori, FUKADA, Takashi, OKA, Shigenori, and SUGIMOTO, Kenji
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The intracellular behavior of human FCHO1 protein was investigated by live-cell imaging microscopy. The fluorescence intensity of green fluorescent protein (GFP)-FCHO1 fluctuated periodically in a perinuclear region approximately every 100 s, reminding us of the periodic fluctuations of clathrin reported in our recent work. The periodicity of FCHO1 was temporally correlated with that of clathrin, suggesting that FCHO1 is involved in clathrin-coated vesicle formation.
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- 2007
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20. Production of Functional Spermatids from Mouse Germline Stem Cells in Ectopically Reconstituted Seminiferous Tubules1
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Kita, Kaoru, Watanabe, Takeshi, Ohsaka, Kimito, Hayashi, Hirofumi, Kubota, Yoshinobu, Nagashima, Yoji, Aoki, Ichiro, Taniguchi, Hideki, Noce, Toshiaki, Inoue, Kimiko, Miki, Hiromi, Ogonuki, Narumi, Tanaka, Hiromitsu, Ogura, Atsuo, and Ogawa, Takehiko
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Testicular germ cell transplantation into the seminiferous tubules is at present the only way to induce spermatogenesis from a given source of spermatogonial stem cells. Here we show an alternative method that harnesses the self-organizing ability of testicular somatic cells. The testicular cells of embryonic or neonatal mice or rats and of newborn pigs were dissociated into single cells. Each of them reorganized into a tubular structure following implantation into the subcutis of immunodeficient mice. When mouse germline stem (GS) cells derived from spermatogonial stem cells and expanded in culture were intermingled with testicular cells of rodents, they were integrated in the reconstituted tubules and differentiated beyond meiosis into spermatids. Normal offspring were produced by the microinjection of those spermatids into oocytes. This method could be applicable to various mammalian species and useful for producing functional gametes from GS cells in a xenoectopic environment.
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- 2007
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21. Leukemia Inhibitory Factor Enhances Formation of Germ Cell Colonies in Neonatal Mouse Testis Culture1
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Kanatsu-Shinohara, Mito, Inoue, Kimiko, Ogonuki, Narumi, Miki, Hiromi, Yoshida, Shosei, Toyokuni, Shinya, Lee, Jiyoung, Ogura, Atsuo, and Shinohara, Takashi
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Spermatogonial stem cells continuously divide in the testis to support spermatogenesis throughout the life of adult male animals. Although very few spermatogonial stem cells are present in vivo, we recently succeeded in expanding these cells in vitro. Germ cells from postnatal testes were able to proliferate in the presence of several types of cytokines, and they formed uniquely shaped colonies of spermatogonia (germline stem or GS cells). These cells reinitiated normal spermatogenesis when transplanted into seminiferous tubules. However, much remains unknown about the contributions of cytokines to successful stem cell culture. In the present study, we examined the role of leukemia inhibitory factor (LIF) in GS cell culture. We found that the addition of LIF to newborn testis cell culture enhances the formation of germ cell colonies. Ciliary neurotrophic factor, but not oncostatin M, had the same effect, although they both bind to the IL-6ST (gp130) receptor. On the other hand, GS cells could be established from pup or adult testes in the absence of LIF. No phenotypic or functional difference was found between GS cells established from different stages, and normal offspring were born from pup-derived GS cells that had been maintained in the absence of LIF, indicating that LIF per se is not involved in the self-renewal of GS cells. These results demonstrate that LIF is useful in the initiation of GS cell culture and suggest that LIF or a related cytokine is involved in the maturation of gonocytes into spermatogonia.
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- 2007
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22. Clonal Origin of Germ Cell Colonies after Spermatogonial Transplantation in Mice1
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Kanatsu-Shinohara, Mito, Inoue, Kimiko, Miki, Hiromi, Ogonuki, Narumi, Takehashi, Masanori, Morimoto, Takeshi, Ogura, Atsuo, and Shinohara, Takashi
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Spermatogenesis originates from a small number of spermatogonial stem cells that can reinitiate spermatogenesis and produce germ cell colonies following transplantation into infertile recipient testes. Although several previous studies have suggested a single-cell origin of germ cell colonies, only indirect evidence has been presented. In this investigation, we tested the clonal origin hypothesis using a retrovirus, which could specifically mark an individual spermatogonial stem cell. Spermatogonial stem cells were infected in vitro with an enhanced green fluorescence protein-expressing retrovirus and subsequently transplanted into infertile recipient mice. Live haploid germ cells were recovered from individual colonies and were microinjected into eggs to create offspring. In total, 45 offspring were produced from five colonies, and 23 (51%) of the offspring were transgenic. Southern blot analysis indicated that the transgenic offspring from the single colony carried a common integration site, and the integration site was different among the transgenic offspring from different colonies. These results provide evidence that germ cell colonies develop from single spermatogonial stem cells.
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- 2006
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23. Anchorage-Independent Growth of Mouse Male Germline Stem Cells In Vitro1
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Kanatsu-Shinohara, Mito, Inoue, Kimiko, Lee, Jiyoung, Miki, Hiromi, Ogonuki, Narumi, Toyokuni, Shinya, Ogura, Atsuo, and Shinohara, Takashi
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Spermatogenesis originates from a small number of spermatogonial stem cells that reside on the basement membrane and undergo self-renewal division to support spermatogenesis throughout the life of adult animals. Although the recent development of a technique to culture spermatogonial stem cells allowed reproduction of self-renewal division in vitro, much remains unknown about how spermatogonial stem cells are regulated. In this study, we found that spermatogonial stem cells could be cultured in an anchorage-independent manner, which is characteristic of stem cells from other types of self-renewing tissues. Although the cultured cells grew slowly (doubling time, ∼4.7 days), they expressed markers of spermatogonia, and grew exponentially for at least 5 months to achieve 1.5 × 1010-fold expansion. The cultured cells underwent spermatogenesis following transplantation into the seminiferous tubules of infertile animals and fertile offspring were obtained by microinsemination of germ cells that had developed within the testes of recipients of the cultured cells. These results indicate that spermatogonial stem cells can undergo anchorage-independent, self-renewal division, and suggest that stem cells have the common property to survive and proliferate in the absence of exogenous substrata.
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- 2006
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24. Variation in Gene Expression and Aberrantly Regulated Chromosome Regions in Cloned Mice1
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Kohda, Takashi, Inoue, Kimiko, Ogonuki, Narumi, Miki, Hiromi, Naruse, Mie, Kaneko-Ishino, Tomoko, Ogura, Atsuo, and Ishino, Fumitoshi
- Abstract
DNA microarray analysis was used to determine the precise genome-wide gene expression profiles of somatic cloned mice derived from Sertoli and cumulus cells. It demonstrated unexpectedly large epigenetic diversity in neonatal cloned mice, despite their normal appearance and genetic identity. In three neonatal tissues of the cloned mice, the expression of 9–40% of the genes examined was more than two times higher or lower in donor cell-dependent or -independent manners compared with normal controls. Relatively few (0.4–4%) of the genes exhibited up- or downregulation in the same manner in both types of clone. A cluster analysis of the variation in gene expression led to the identification of several chromosome regions in which gene expression was aberrantly controlled in the somatic clones. These results provide a more complete understanding of how somatic clones differ from each other and from normal individuals produced by sexual reproduction and indicate the significant difficulties that face the application of somatic cloning in regenerative medicine.
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- 2005
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25. Long-Term Culture of Mouse Male Germline Stem Cells Under Serum-or Feeder-Free Conditions1
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Kanatsu-Shinohara, Mito, Miki, Hiromi, Inoue, Kimiko, Ogonuki, Narumi, Toyokuni, Shinya, Ogura, Atsuo, and Shinohara, Takashi
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Spermatogonial stem cells are the only stem cells in the body that transmit genetic information to the next generation. These cells can be cultured for extended periods in the presence of serum and feeder cells. However, little is known about factors that regulate self-renewal division of spermatogonial stem cells. In this investigation we examined the possibility of establishing culture systems for spermatogonial stem cells that lack serum or a feeder cell layer. Spermatogonial stem cells could expand in serum-free conditions on mouse embryonic fibroblasts (MEFs), or were successfully cultivated without feeder cells on a laminin-coated plate. However, they could not expand when both serum and feeder cells were absent. Although the cells cultured on laminin differed phenotypically from those on feeder cells, they grew exponentially for at least 6 mo, and produced normal, fertile progeny following transplantation into infertile mouse testis. This culture system will provide a new opportunity for understanding the regulatory mechanism that governs spermatogonial stem cells.
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- 2005
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26. Visualization of chromosomes and nuclear envelope in living cells for molecular dynamics studies
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Fukada, Takashi, Inoue, Kimiko, Urano, Takeshi, and Sugimoto, Kenji
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- 2004
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27. The Novel Dominant Mutation DspdLeads to a Severe Spermiogenesis Defect in Mice1
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Kai, Masayuki, Irie, Masahito, Okutsu, Tomohisa, Inoue, Kimiko, Ogonuki, Narumi, Miki, Hiromi, Yokoyama, Minesuke, Migishima, Rika, Muguruma, Kaori, Fujimura, Hisako, Kohda, Takashi, Ogura, Atsuo, Kaneko-Ishino, Tomoko, and Ishino, Fumitoshi
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Spermiogenesis is a complex process that is regulated by a plethora of genes and interactions between germ and somatic cells. Here we report a novel mutant mouse strain that carries a transgene insertional/translocational mutation and exhibits dominant male sterility. We named the mutation dominant spermiogenesis defect (Dspd). In the testes of Dspdmutant mice, spermatids detached from the seminiferous epithelium at different steps of the differentiation process before the completion of spermiogenesis. Microinsemination using spermatids collected from the mutant testes resulted in the birth of normal offspring. These observations indicate that the major cause of Dspdinfertility is (are) a defect(s) in the Sertoli cell-spermatid interaction or communication in the seminiferous tubules. Fluorescent in situ hybridization (FISH) analysis revealed a translocation between chromosomes 7F and 14C at the transgene insertion site. The deletion of a genomic region of chromosome 7F greater than 1 megabase and containing at least six genes (Cttn, Fadd, Fgf3, Fgf4, Fgf15,and Ccnd1) was associated with the translocation. Cttnencodes the actin-binding protein cortactin. Immunohistochemical analysis revealed localization of cortactin beside elongated spermatids in wild-type testes; abnormality of cortactin localization was found in mutant testes. These data suggest an important role of cortactin in Sertoli cell-spermatid interactions and in the Dspdphenotype.
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- 2004
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28. Effects of Donor Cell Type and Genotype on the Efficiency of Mouse Somatic Cell Cloning1
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Inoue, Kimiko, Ogonuki, Narumi, Mochida, Keiji, Yamamoto, Yoshie, Takano, Kaoru, Kohda, Takashi, Ishino, Fumitoshi, and Ogura, Atsuo
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Although it is widely assumed that the cell type and genotype of the donor cell affect the efficiency of somatic cell cloning, little systematic analysis has been done to verify this assumption. The present study was undertaken to examine whether donor cell type, donor genotype, or a combination thereof increased the efficiency of mouse cloning. Initially we assessed the developmental ability of embryos that were cloned from cumulus or immature Sertoli cells with six different genotypes (i.e., 2 × 6 factorial). Significantly better cleavage rates were obtained with cumulus cells than with Sertoli cells (P< 0.005, two-way ANOVA), which probably was due to the superior cell-cycle synchrony of cumulus cells at G0/G1. After embryo transfer, there was a significant effect of cell type on the birth rate, with Sertoli cells giving the better result (P< 0.005). Furthermore, there was a significant interaction (P< 0.05) between the cell type and genotype, which indicates that cloning efficiency is determined by a combination of these two factors. The highest mean birth rate (10.8 ± 2.1%) was obtained with (B6 × 129)F1 Sertoli cells. In the second series of experiments, we examined whether the developmental ability of clones with the wild-type genotype (JF1) was improved when combined with the 129 genotype. Normal pups were cloned from cumulus and immature Sertoli cells of the (129 × JF1)F1 and (JF1 × 129)F1 genotypes, whereas no pups were born from cells with the (B6 × JF1)F1 genotype. The present study clearly demonstrates that the efficiency of somatic cell cloning, and in particular fetal survival after embryo transfer, may be improved significantly by choosing the appropriate combinations of cell type and genotype.
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- 2003
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29. Long-Term Proliferation in Culture and Germline Transmission of Mouse Male Germline Stem Cells1
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Kanatsu-Shinohara, Mito, Ogonuki, Narumi, Inoue, Kimiko, Miki, Hiromi, Ogura, Atsuo, Toyokuni, Shinya, and Shinohara, Takashi
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Spermatogenesis is a complex process that originates in a small population of spermatogonial stem cells. Here we report the in vitro culture of spermatogonial stem cells that proliferate for long periods of time. In the presence of glial cell line-derived neurotrophic factor, epidermal growth factor, basic fibroblast growth factor, and leukemia inhibitory factor, gonocytes isolated from neonatal mouse testis proliferated over a 5-month period (>1014-fold) and restored fertility to congenitally infertile recipient mice following transplantation into seminiferous tubules. Long-term spermatogonial stem cell culture will be useful for studying spermatogenesis mechanism and has important implications for developing new technology in transgenesis or medicine.
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- 2003
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30. Fertilization of Oocytes and Birth of Normal Pups Following Intracytoplasmic Injection with Spermatids in Mastomys (Praomys coucha)1
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Ogonuki, Narumi, Mochida, Keiji, Inoue, Kimiko, Matsuda, Junichiro, Yamamoto, Yoshie, Takano, Kaoru, and Ogura, Atsuo
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The mastomys is a small laboratory rodent that is native to Africa. Although it has been used for research concerning reproductive biology, in vitro fertilization (IVF) and intracytoplasmic sperm injection are very difficult in mastomys because of technical problems, such as inadequate sperm capacitation and large sperm heads. The present study was undertaken to examine whether mastomys spermatids could be used to fertilize oocytes in vitro using a microinsemination technique, because spermatids are more easily injected than mature spermatozoa into oocytes. Most mastomys oocytes (80%–90%) survived intracytoplasmic injection with either round or elongated spermatids. Round spermatids had little oocyte-activating capacity, similar to those of mice and rats, and exogenous stimuli were needed for normal fertilization. Treatment with an electric pulse in the presence of 50 μM Ca2+followed by culture in 10 mM SrCl2led to successful oocyte activation. After injection of round spermatids into preactivated oocytes, 93% of oocytes were normally fertilized (male and female pronuclei formed), and 100% of cultured oocytes developed to the 2-cell stage. However, none reached term after transfer into recipient females. Elongated spermatids, which correspond to steps 9–11 in rats, activated oocytes on injection without additional activation treatment. After embryo transfer, five offspring (6% per transfer) developed to term. These results indicate that microinsemination with spermatids is a feasible alternative in animal species that are refractory to IVF and sperm injection and that using later-stage spermatids may lead to increased production of viable embryos that can develop into normal offspring.
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- 2003
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31. Allogeneic Offspring Produced by Male Germ Line Stem Cell Transplantation into Infertile Mouse Testis1
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Kanatsu-Shinohara, Mito, Ogonuki, Narumi, Inoue, Kimiko, Ogura, Atsuo, Toyokuni, Shinya, Honjo, Tasuku, and Shinohara, Takashi
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The testis is one of several immune-privileged organs and is known for its unique ability to support allogeneic or xenogeneic tissue transplants. We investigated the possibility of deriving offspring from mice that underwent transplantation with allogeneic male germ line stem cells in the testis. Although mature adult mice rejected allogeneic germ cells and were infertile, offspring were obtained by intracytoplasmic germ cell injection using partially differentiated donor cells. In contrast, complete spermatogenesis occurred when allogeneic germ cells were transplanted into immature pup testes. Tolerance induction by monoclonal antibody administration allowed the pup transplant recipients to produce allogeneic offspring by natural mating, whereas no spermatozoa were found in the epididymis of untreated recipients. Thus, these results indicate that a histoincompatible recipient can serve as a “surrogate father” to propagate the genetic information of heterologous male donors.
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- 2003
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32. Epigenetic regulation in mammalian development and dysfunction: the effects of somatic cloning and genomic imprinting
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Kohda, Takashi, Lee, Jiyoung, Inoue, Kimiko, Ogonuki, Natumi, Wakisaka-Saito, Noriko, Kaneko-Ishino, Tomoko, Ogura, Atsuo, and Ishino, Fumitoshi
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Although somatic cell cloning has been accomplished in several mammalian species, its efficiency remains considerably low due to fetal mortality during the pre- and perinatal periods, which suggests incomplete initialization of epigenetic memories during the somatic cloning procedure. Genomic imprinting is an epigenetic mechanism that produces functional differences between the paternal and maternal genomes, and plays an essential role in mammalian development and growth. Therefore, it is very important to examine the genomic imprinting status of somatic clones. The placenta is one of the most commonly affected organs in the somatic clones. We confirmed that parental-origin-specific monoallelic expression of imprinted genes was maintained faithfully in cloned embryos and abnormal placentas. However, reduced expression was observed for several genes, including certain imprinted genes in both day 12.5 and term placentas. These results suggest that the development process in cloned mice is not identical to that in normal mice. We analyzed mouse clone embryos, which were produced from primordial germ cells (PGCs), and characterized the initialization of the parental imprinted memories. Memory erasure proceeded in a step-wise manner and was coordinated specifically for each imprinted gene at embryonic day 11.5, followed by the establishment of default imprinting states that were common to both male and female germ lines.
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- 2002
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33. Improved Postimplantation Development of Rabbit Nuclear Transfer Embryos by Activation with Inositol 1,4,5-Trisphosphate
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Inoue, Kimiko, Ogonuki, Narumi, Yamamoto, Yoshie, Noguchi, Yoko, Takeiri, Shuji, Nakata, Kumiko, Miki, Hiromi, Kurome, Mayuko, Nagashima, Hiroshi, and Ogura, Atsuo
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Cloned rabbit embryos are characterized by their extremely poor postimplantation development, despite their high survivability until the blastocyst stage in vitro. This study examined whether the developmental failure of cloned rabbit embryos in vivo can be overcome by technical improvements to the activation protocol. Freshly collected cumulus cells were transferred into enucleated oocytes by intracytoplasmic injection. One to two hours later, the oocytes were activated by electroporation with Ca2+ or inositol 1,4,5-trisphosphate (IP3), which is known to induce repeated rises in intracellular Ca2+, as in normal fertilization. After transfer of embryos at the two- to four-cell stages, well-defined implantation sites with remnant fetal tissue were observed at term (day 28) only in the IP3-stimulation groups (0.9% and 5.8% per transferred embryo for single and triple stimulation groups, respectively). When some recipients in the same group were examined at days 16-20, a viable cloned fetus (day 19) with normal organogenesis was obtained. These findings clearly demonstrate that the oocyte activation protocol using IP3 enhances the postimplantation development of nuclear-transferred rabbit embryos.
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- 2002
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34. Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells
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Lee, Jiyoung, Inoue, Kimiko, Ono, Ryuichi, Ogonuki, Narumi, Kohda, Takashi, Kaneko-Ishino, Tomoko, Ogura, Atsuo, and Ishino, Fumitoshi
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Genomic imprinting is an epigenetic mechanism that causes functional differences between paternal and maternal genomes, and plays an essential role in mammalian development. Stage-specific changes in the DNA methylation patterns of imprinted genes suggest that their imprints are erased some time during the primordial germ cell (PGC) stage, before their gametic patterns are re-established during gametogenesis according to the sex of individuals. To define the exact timing and pattern of the erasure process, we have analyzed parental-origin-specific expression of imprinted genes and DNA methylation patterns of differentially methylated regions (DMRs) in embryos, each derived from a single day 11.5 to day 13.5 PGC by nuclear transfer. Cloned embryos produced from day 12.5 to day 13.5 PGCs showed growth retardation and early embryonic lethality around day 9.5. Imprinted genes lost their parental-origin-specific expression patterns completely and became biallelic or silenced. We confirmed that clones derived from both male and female PGCs gave the same result, demonstrating the existence of a common default state of genomic imprinting to male and female germlines. When we produced clone embryos from day 11.5 PGCs, their development was significantly improved, allowing them to survive until at least the day 11.5 embryonic stage. Interestingly, several intermediate states of genomic imprinting between somatic cell states and the default states were seen in these embryos. Loss of the monoallelic expression of imprinted genes proceeded in a step-wise manner coordinated specifically for each imprinted gene. DNA demethylation of the DMRs of the imprinted genes in exact accordance with the loss of their imprinted monoallelic expression was also observed. Analysis of DNA methylation in day 10.5 to day 12.5 PGCs demonstrated that PGC clones represented the DNA methylation status of donor PGCs well. These findings provide strong evidence that the erasure process of genomic imprinting memory proceeds in the day 10.5 to day 11.5 PGCs, with the timing precisely controlled for each imprinted gene. The nuclear transfer technique enabled us to analyze the imprinting status of each PGC and clearly demonstrated a close relationship between expression and DNA methylation patterns and the ability of imprinted genes to support development.
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- 2002
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35. Mito-mice: animal models for mitochondrial DNA-based diseases
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Nakada, Kazuto, Inoue, Kimiko, and Hayashi, Jun-Ichi
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We have successfully produced ‘Mito-mice’ harbouring a pathogenic mtDNA mutation. We generated the mice by introducing mitochondria with a 4696 base-pair mtDNA deletion (ΔmtDNA4696) into mouse embryos. This deletion encompasses nucleotides 7759–12 454 and includes six tRNA genes and seven structural genes. In Mito-mice, the ΔmtDNA4696 is transmitted maternally, and induces mitochondrial dysfunction in various tissues. Most of the Mito-mice with high proportions of the ΔmtDNA4696 died at about age 6 months due to renal failure. Mito-mice are the first animal model for mtDNA-based diseases and will be valuable for studying pathogenesis and for identifying effective drug and gene therapies.
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- 2001
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36. Correlation of Functional and Ultrastructural Abnormalities of Mitochondria in Mouse Heart Carrying a Pathogenic Mutant mtDNA with a 4696-bp Deletion
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Nakada, Kazuto, Inoue, Kimiko, Chen, Chu-Shih, Nonaka, Ikuya, Goto, Yu-ichi, Ogura, Atsuo, and Hayashi, Jun-Ichi
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We examined the correlation of functional and structural abnormalities of cardiac mitochondria created by pathogenic mutant mtDNAs using mito-mice with hearts carrying 88% mutant ΔmtDNA4696 with a 4696 deletion. COX histochemistry, quantitative PCR analysis, and electronmicrographs showed that accumulation of 91.6% ΔmtDNA4696 in single cardiac muscle fibers induced progressive reduction of COX activity to form COX-negative fibers. Moreover, hearts carrying 88% ΔmtDNA4696 consisted of three types of cardiac muscle fibers with different functional properties, COX-positive, -negative, and -intermediate fibers, which corresponded respectively to three types of fibers with different structural properties; type A fibers containing mitochondria with only lamellar cristae, type B containing mitochondria with only tubular cristae, and type C possessing mitochondria with both lamellar and tubular cristae. These observations suggest that lamellar cristae with COX activity transform into tubular cristae without COX activity along with the accumulation of ΔmtDNA4696, which would be responsible for insufficient supply of mtDNA products required to keep the normal structure and function of mitochondrial cristae. The correlation of these structural and functional abnormalities of cristae should provide important insight into diagnosis of cardiomyopathies caused by accumulation of pathogenic mutant mtDNAs.
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- 2001
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37. Interaction Theory of Mammalian Mitochondria
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Nakada, Kazuto, Inoue, Kimiko, and Hayashi, Jun-Ichi
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We generated mice with deletion mutant mtDNA by its introduction from somatic cells into mouse zygotes. Expressions of disease phenotypes are limited to tissues expressing mitochondrial dysfunction. Considering that all these mice share the same nuclear background, these observations suggest that accumulation of the mutant mtDNA and resultant expressions of mitochondrial dysfunction are responsible for expression of disease phenotypes. On the other hand, mitochondrial dysfunction and expression of clinical abnormalities were not observed until the mutant mtDNA accumulated predominantly. This protection is due to the presence of extensive and continuous interaction between exogenous mitochondria from cybrids and recipient mitochondria from embryos. Thus, we would like to propose a new hypothesis on mitochondrial biogenesis, interaction theory of mitochondria: mammalian mitochondria exchange genetic contents, and thus lost the individuality and function as a single dynamic cellular unit.
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- 2001
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38. Homozygosity Mapping to Chromosome 5p15 of a Gene Responsible for Hartnup Disorder
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Nozaki, Jun-ichi, Dakeishi, Miwako, Ohura, Toshihiro, Inoue, Kimiko, Manabe, Motomu, Wada, Yasuhiko, and Koizumi, Akio
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Hartnup disorder is an autosomal recessive phenotype involving a transporter for monoamino-monocarboxylic acids. Genetic analysis of the mouse model mapped its locus to human chromosome 11q13 (8). We report here the results of linkage analysis in two Japanese first cousin-marriage families. In the first family, the proband had Hartnup disorder and his deceased older brother was reported to have had typical Hartnup symptoms. The younger brother of the proband was shown to have decreased tryptophan absorption by oral loading test. In the second family, a 6-year-old girl, the proband, had specific hyperaminoaciduria. DNA was isolated from either blood samples or umbilical cord stumps. Genome-wide screening by homozygosity mapping was conducted. Taking into account that the older brother was affected and the younger brother was a carrier in the first family, homozygosity mapping (LOD score = 3.55) and GENEHUNTER (LOD score = 3.28) locates the locus of the Hartnup disorder on 5p15.
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- 2001
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39. Production of Male Cloned Mice from Fresh, Cultured, and Cryopreserved Immature Sertoli Cells1
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Ogura, Atsuo, Inoue, Kimiko, Ogonuki, Narumi, Noguchi, Akira, Takano, Kaoru, Nagano, Reiko, Suzuki, Osamu, Lee, Jiyoung, Ishino, Fumitoshi, and Matsuda, Junichiro
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Although it is generally accepted that relatively high efficiencies of somatic cell cloning in mammals can be achieved by using donor cells from the female reproductive system (e.g., cumulus/granulosa, oviduct, and mammary gland cells), there is little information on the possibility of using male-specific somatic cells as donor cells. In this study we injected the nucleus of immature mouse Sertoli cells isolated from the testes of newborn (Days 3–10) males into enucleated mature oocytes in order to examine the ability of their nuclei to support embryonic development. After activation of the oocytes that had received the freshly recovered immature Sertoli cells, some developed into the morula/blastocyst stage, depending on the age of the donor cells (22.0–37.4%). When transferred into pseudopregnant females, 7 (3.3%, 7 of 215) developed into normal pups at term. Nuclear transfer of immature Sertoli cells after 1 wk in culture also produced normal pups after embryo transfer (3.1%, 2 of 65). Even after cryopreservation in a conventional cryoprotectant solution, their ability as donor cells was maintained, as demonstrated by the birth of cloned young (6.7%, 7 of 105). Immature Sertoli cells transfected with green fluorescent protein gene also supported embryo development into morulae/blastocysts, which showed specific fluorescence. This study demonstrates that immature Sertoli cells, male-specific somatic cells, are potential donors for somatic cell cloning.
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- 2000
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40. Spermatogenesis. Mouse spermatid nuclei can support full term development after premature chromosome condensation within mature oocytes
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Ogura, Atsuo, Inoue, Kimiko, and Matsuda, Junichiro
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The nucleus of round spermatids, the earliest haploid male germ cells, can participate in the formation of normal zygotes when incorporated into activated oocytes. In this study, we injected mouse round spermatids into homologous mature oocytes that were kept arrested at metaphase II to induce premature chromosome condensation (PCC) of the spermatid nuclei. After full condensation of the spermatid chromosomes, the oocytes were activated by Sr2+-containing medium, into which cytochalasin B was added to prevent extrusion of the segregated female and male chromosomes as polar bodies. Out of 142 oocytes examined, 104 (73%) formed two male (pseudo)pronuclei and two female pronuclei. To restore the diploid state of these zygotes, one of the female pronuclei was removed. When cultured in vitro for 72 hours, all (n = 37) of the constructed embryos developed to the morula/blastocyst stage. When 2-cell embryos and morulae/blastocysts were transferred into pseudopregnant females, 14 (13/96) and 24% (9/37), respectively, developed into term offspring. This study indicates that the spermatid chromosomes, which had undergone PCC, moved safely to opposite poles after oocyte activation. Since round spermatids contain no (in the mouse) or little (in patients with spermatogenic failure) oocyte-activating factor, this method may be used to rescue oocytes that fail to be activated at the time of spermatid injection.
- Published
- 1999
41. Long-Term Postmortem Survival of Mitochondrial Genomes in Mouse Synaptosomes and Their Rescue in a Mitochondrial DNA-less Mouse Cell Line
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Ito, Sayaka, Inoue, Kimiko, Yanagisawa, Nami, Kaneko, Motohisa, and Hayashi, Jun-Ichi
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Mitochondrial DNA (mtDNA) transfer was carried out from postmortem mouse tissues to mouse mtDNA-less (ρ0) cells to determine how long it takes for autolysis of mtDNA after death and whether mtDNA in postmortem tissues can recover its function in ρ0cells. The results showed that mtDNA was stable in postmitotic tissues stored at 4°C. Moreover, mtDNA in postmortem brain tissues stored for up to 1 month still retained functional properties, causing complete recovery of mitochondrial respiratory function, when it was transferred to ρ0cells. These observations suggest that mtDNA in brain tissue can survive for 1 month after death and can start replication and gene expression in ρ0cells without showing any functional defects. This procedure might be applied to human autopsy brain tissues for examination of the influence of accumulated somatic mutations in mtDNA from aged subjects.
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- 1998
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42. Isolation and Characterization of Mitochondrial DNA-less Lines from Various Mammalian Cell Lines by Application of an Anticancer Drug, Ditercalinium
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Inoue, Kimiko, Takai, Daisaku, Hosaka, Hideka, Ito, Sayaka, Shitara, Hiroshi, Isobe, Kotoyo, Lepecq, Jean-Bernard, Segal-Bendirdjian, Evelyne, and Hayashi, Jun-Ichi
- Abstract
Since ethidium bromide was not effective in mouse cell lines for isolating mitochondrial DNA (mtDNA)-less cells (ρ0cells), we examined whether an anticancer drug, ditercalinium (DC), which has been shown to exclude mtDNA from mouse cell lines, could be effective in various mouse and human cell lines. We found that after DC treatment ρ0cells could be isolated from all cell lines of mouse or human origin tested. Moreover, these ρ0cells maintained ability to receive exogenously imported mtDNA and allow its replication and gene expression. These observations suggest that DC eliminates mtDNA from mouse and human cells without affecting the property to receive exogenous mtDNA. Therefore, DC could be applicable to cell lines expressing various differentiated phenotypes for studying whether mtDNA plays a significant role in expression of phenotypes by manipulating mtDNA elimination and reintroduction.
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- 1997
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43. Isolation of Mitochondrial DNA-less Mouse Cell Lines and Their Application for Trapping Mouse Synaptosomal Mitochondrial DNA with Deletion Mutations*
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Inoue, Kimiko, Ito, Sayaka, Takai, Daisaku, Soejima, Aki, Shisa, Hayase, LePecq, Jean-Bernard, Segal-Bendirdjian, Evelyne, Kagawa, Yasuo, and Hayashi, Jun-Ichi
- Abstract
For isolation of mouse mtDNA-less (ρ0) cell lines, we searched for various antimitochondrial drugs that were expected to decrease the mtDNA content and found that treatment with ditercalinium, an antitumor bis-intercalating agent, was extremely effective for completely excluding mtDNA in all the mouse cell lines we tested. The resulting ρ0mouse cells were successfully used for trapping the mtDNA of living nerve cells into dividing cultured cells by fusion of the ρ0cells with mouse brain synaptosomes, which represent synaptic endings isolated from nerve cells. With neuronal mtDNA obtained, all of the cybrid clones restored mitochondrial translation activity similarly regardless of whether the mtDNA was derived from young or aged mice, thus at least suggesting that defects in mitochondrial genomes are not involved in the age-associated mitochondrial dysfunction observed in the brain of aged mice. Furthermore, we could trap a very small amount of a common 5823-base pair deletion mutant mtDNA (ΔmtDNA5823) that was detectable by polymerase chain reaction in the cybrid clones. As the amount of mutant mtDNA with large scale deletions was expected to increase during prolonged cultivation of the cybrids, these cells should be available for establishment of mice containing the deletion mutant mtDNA.
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- 1997
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44. Mutant mtDNA at 1555 A to G in 12S rRNA Gene and Hypersusceptibility of Mitochondrial Translation to Streptomycin Can Be Co-Transferred to ρ0HeLa Cells
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Inoue, Kimiko, Takai, Daisaku, Soejima, Aki, Isobe, Kotoyo, Yamasoba, Tatsuya, Oka, Yoshitomo, Goto, Yu-ichi, and Hayashi, Jun-Ichi
- Abstract
Human skin fibroblast line 95–119, which had been isolated from the mother of a Japanese patient with aminoglycoside-induced deafness and a 1555 A to G mutation at 12S rRNA gene in mitochondrial DNA (mtDNA), was used to investigate the relationship between the 1555 mtDNA mutation and its pathogenicity. By the intercellular transfer of mtDNA with or without the 1555 mutation to mtDNA-less (ρ0) HeLa cells, we isolated cybrid clones and found that the mitochondrial translation in a cybrid clone repopulated with the homoplasmic 1555 mutation showed the highest susceptibility to streptomycin. These observations suggest that the genotype of the mutant mtDNA and the phenotype of hypersusceptibility to streptomycin observed in 95–119 fibroblasts were co-transferred simultaneously to ρ0HeLa cells, supporting the idea that the homoplasmic 1555 mtDNA mutation is involved in the pathogenesis leading to aminoglycoside-induced hearing loss.
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- 1996
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45. The Interorganellar Interaction between Distinct Human Mitochondria with Deletion Mutant mtDNA from a Patient with Mitochondrial Disease and with HeLa mtDNA*
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Takai, Daisaku, Inoue, Kimiko, Goto, Yu-ichi, Nonaka, Ikuya, and Hayashi, Jun-Ichi
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For the examination of possible intermitochondrial interaction of human mitochondria from different cells, cybrids were constructed by introducing HeLa mitochondria into cells with respiration-deficient (ρ−) mitochondria. Respiration deficiency was due to the predominance of mutant mtDNA with a 5,196-base pair deletion including five tRNA genes (ΔmtDNA5196). The HeLa mtDNA and ΔmtDNA5196encoded chloramphenicol-resistant (CAPr) and chloramphenicol-sensitive (CAPs) 16 S rRNA, respectively. The first evidence for the interaction was that polypeptides exclusively encoded by ΔmtDNA5196were translated on the introduction of HeLa mitochondria, suggesting supplementation of the missing tRNAs by ρ−mitochondria from HeLa mitochondria. Second, the exchange of mitochondrial rRNAs was observed; even in the presence of CAP, CAPsΔmtDNA5196-specific polypeptides as well as those encoded by CAPrHeLa mtDNA were translated in the cybrids. These phenomena can be explained assuming that the translation in ρ−mitochondria was restored by tRNAs and CAPr16 S rRNA supplied from HeLa mitochondria, unambiguously indicating interorganellar interaction. These observations introduce a new concept of the dynamics of the mitochondrial genetic system and help in understanding the relationship among mtDNA mutations and expression of human mitochondrial diseases and aging.
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- 1997
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46. Loss of H3K27me3 Imprinting in Somatic Cell Nuclear Transfer Embryos Disrupts Post-Implantation Development
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Matoba, Shogo, Wang, Huihan, Jiang, Lan, Lu, Falong, Iwabuchi, Kumiko A., Wu, Xiaoji, Inoue, Kimiko, Yang, Lin, Press, William, Lee, Jeannie T., Ogura, Atsuo, Shen, Li, and Zhang, Yi
- Abstract
Animal cloning can be achieved through somatic cell nuclear transfer (SCNT), although the live birth rate is relatively low. Recent studies have identified H3K9me3 in donor cells and abnormal Xistactivation as epigenetic barriers that impede SCNT. Here we overcome these barriers using a combination of Xistknockout donor cells and overexpression of Kdm4to achieve more than 20% efficiency of mouse SCNT. However, post-implantation defects and abnormal placentas were still observed, indicating that additional epigenetic barriers impede SCNT cloning. Comparative DNA methylome analysis of IVF and SCNT blastocysts identified abnormally methylated regions in SCNT embryos despite successful global reprogramming of the methylome. Strikingly, allelic transcriptomic and ChIP-seq analyses of pre-implantation SCNT embryos revealed complete loss of H3K27me3 imprinting, which may account for the postnatal developmental defects observed in SCNT embryos. Together, these results provide an efficient method for mouse cloning while paving the way for further improving SCNT efficiency.
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- 2018
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47. P39. Enhancer of Polycomb 1 is essential for spermiogenesis by regulating histone hyperacetylation status
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Dong, Yixin, Takada, Yuki, Isono, Kyo-ichi, Ohbo, Kazuyuki, Ogonuki, Narumi, Ogura, Atsuo, Inoue, Kimiko, Toyama, Yoshiro, Maekawa, Mamiko, Toshimori, Kiyotaka, and Koseki, Haruhiko
- Abstract
During spermiogenesis, the post-meiotic stage of spermatogenesis, the chromatin structure of spermatid undergoes dramatic changes: histones are replaced with transition proteins and subsequently with protamines, and the global chromatin is highly condensed. Histone acetylation results in a loose nucleosomal structure, and is believed to facilitate this chromatin transformation. Histone hyperacetylation emerges from step 8 round spermatid and elongating spermatid which are the initial steps of chromatin reorganization. The mechanisms responsible for this global histone modification are poorly understood. Here we showed that the deletion of murine Enhancer of Polycomb 1 (Epc1, a homologue of Drosophila Epc whose mutations enhancing the phenotypes of other Polycomb group mutants) resulted in an arrest of spermiogenesis at step 7 round spermatid coincidently with an evanescence of histone hyperacetylation. We further found that Epc1 associated with a histone acetyltransferase Tip60 in testis, and the depletion of Epc1 severely disrupted the distribution of Tip60. In some individuals, a few spermatids escaped from the arrest and their chromatin was recaptured with acetylated histones and incorporated with transition protein 2, although their levels were much lower than normal elongating spermatids. Treatment with TSA, a histone deacetylase inhibitor, also increased the incorporation of transition protein 2 into Epc1−/−spermatids. These data demonstrated that Epc1 associating with Tip60 plays an important role in histone hyperacetylation during male germ cell development.
- Published
- 2010
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48. Cellular Dynamics of Mouse Trophoblast Stem Cells: Identification of a Persistent Stem Cell Type1
- Author
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Motomura, Kaori, Oikawa, Mami, Hirose, Michiko, Honda, Arata, Togayachi, Sumie, Miyoshi, Hiroyuki, Ohinata, Yasuhide, Sugimoto, Michihiko, Abe, Kuniya, Inoue, Kimiko, and Ogura, Atsuo
- Abstract
Mouse trophoblast stem cells (TSCs) proliferate indefinitely in vitro, despite their highly heterogeneous nature. In this study, we sought to characterize TSC colony types by using methods based on cell biology and biochemistry for a better understanding of how TSCs are maintained over multiple passages. Colonies of TSCs could be classified into four major types: type 1 is compact and dome-shaped, type 4 is flattened but with a large multilayered cell cluster, and types 2 and 3 are their intermediates. A time-lapse analysis indicated that type 1 colonies predominantly appeared after passaging, and a single type 1 colony gave rise to all other types. These colony transitions were irreversible, but at least some type 1 colonies persisted throughout culture. The typical cells comprising type 1 colonies were small and highly motile, and they aggregated together to form primary colonies. A hierarchical clustering based on global gene expression profiles suggested that a TSC line containing more type 1 colony cells was similar to in vivo extraembryonic tissues. Among the known TSC genes examined, Elf5showed a differential expression pattern according to colony type, indicating that this gene might be a reliable marker of undifferentiated TSCs. When aggregated with fertilized embryos, cells from types 1 and 2, but not from type 4, distributed to the polar trophectoderm in blastocysts. These findings indicate that cells typically found in type 1 colonies can persist indefinitely as stem cells and are responsible for the maintenance of TSC lines. They may provide key information for future improvements in the quality of TSC lines.
- Published
- 2016
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49. Generation of Cloned Mice from Adult Neurons by Direct Nuclear Transfer1
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Mizutani, Eiji, Oikawa, Mami, Kassai, Hidetoshi, Inoue, Kimiko, Shiura, Hirosuke, Hirasawa, Ryutaro, Kamimura, Satoshi, Matoba, Shogo, Ogonuki, Narumi, Nagatomo, Hiroaki, Abe, Kuniya, Wakayama, Teruhiko, Aiba, Atsu, and Ogura, Atsuo
- Abstract
Whereas cloning mammals by direct somatic cell nuclear transfer has been successful using a wide range of donor cell types, neurons from adult brain remain “unclonable” for unknown reasons. Here, using a combination of two epigenetic approaches, we examined whether neurons from adult mice could be cloned. First, we used a specific antibody to discover cell types with reduced amounts of a repressive histone mark—dimethylated histone H3 lysine 9 (H3K9me2)—and identified CA1 pyramidal cells in the hippocampus and Purkinje cells in the cerebellum as candidates. Second, reconstructed embryos were treated with trichostatin A (TSA), a potent histone deacetylase inhibitor. Using CA1 cells, cloned offspring were obtained at high rates, reaching 10.2% and 4.6% (of embryos transferred) for male and female donors, respectively. Cerebellar Purkinje cell nuclei were too large to maintain their genetic integrity during nuclear transfer, leading to developmental arrest of embryos. However, gene expression analysis using cloned blastocysts corroborated a high rate of genomic reprogrammability of CA1 pyramidal and Purkinje cells. Neurons from the hippocampal dentate gyrus and cerebral cortex, which had higher amounts of H3K9me2, could also be used for producing cloned offspring, but the efficiencies were low. A more thorough analysis revealed that TSA treatment was essential for cloning adult neuronal cells. This study demonstrates, to our knowledge for the first time, that adult neurons can be cloned by nuclear transfer. Furthermore, our data imply that reduced amounts of H3K9me2 and increased histone acetylation appear to act synergistically to improve the development of cloned embryos
- Published
- 2015
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50. Establishment of Paternal Genomic Imprinting in Mouse Prospermatogonia Analyzed by Nuclear Transfer1
- Author
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Kamimura, Satoshi, Hatanaka, Yuki, Hirasawa, Ryutaro, Matsumoto, Kazuya, Oikawa, Mami, Lee, Jiyoung, Matoba, Shogo, Mizutani, Eiji, Ogonuki, Narumi, Inoue, Kimiko, Kohda, Takashi, Ishino, Fumitoshi, and Ogura, Atsuo
- Abstract
In mice, the establishment of paternal genomic imprinting in male germ cells starts at midgestation, as suggested by DNA methylation analyses of differentially methylated regions (DMRs). However, this information is based on averages from mixed populations of germ cells, and the DNA methylation pattern might not always provide a full representation of imprinting status. To obtain more detailed information on the establishment of paternal imprinting, single prospermatogonia at Embryonic Days 15.5 (E15.5), E16.5, and E17.5 and at Day 0.5 after birth were cloned using nuclear transfer; previous reports suggested that cloned embryos reflected the donor's genomic imprinting status. Then, the resultant fetuses (E9.5) were analyzed for the DNA methylation pattern of three paternal DMRs (IG-DMR, H19DMR, and Rasgrf1DMR) and the expression pattern of imprinted genes therein. The overall data indicated that establishment of genomic imprinting in all paternally imprinted regions was completed by E17.5, following a short intermediate period at E16.5. Furthermore, comparison between the methylation status of DMRs and the expression profiles of imprinted genes suggested that methylation of the IG-DMR, but not the H19DMR, solely governed the control of its imprinted gene cluster. The Rasgrf1DMR seemed to be imprinted later than the other two genes. We also found that the methylation status of the Gtl2DMR, the secondary DMR that acquires DNA methylation after fertilization, was likely to follow the methylation status of the upstream IG-DMR. Thus, the systematic analyses of prospermatogonium-derived embryos provided additional important information on the establishment of paternal imprinting.
- Published
- 2014
- Full Text
- View/download PDF
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