13 results on '"Yuko Kagawa"'
Search Results
2. The impact of adjuvant surgical treatment of nontuberculous mycobacterial pulmonary disease on prognosis and outcome
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Kiyoharu Fukushima, Mari Miki, Yuki Matsumoto, Emi Uda, Yuji Yamamoto, Yuya Kogita, Yuko Kagawa, Takanori Matsuki, Hiroyuki Kagawa, Yohei Oshitani, Daisuke Motooka, Kazuyuki Tsujino, Kenji Yoshimura, Keisuke Miki, Akio Hayashi, Shota Nakamura, Seigo Kitada, Yukiyasu Takeuchi, and Hiroshi Kida
- Subjects
Nontuberculous mycobacteria ,Mycobacterium avium ,Mycobacterium abscessus ,Thoracic surgery ,Diseases of the respiratory system ,RC705-779 - Abstract
Abstract Background Lung resection in patients with nontuberculous mycobacterial pulmonary disease (NTM-PD) has been reported to be associated with favorable outcomes. However, little is known regarding the risk and prognostic factors for refractory and recurrent cases. We aimed to evaluate the overall impact and benefit of adjuvant lung surgery by comparing NTM-PD patients who underwent adjuvant lung resection with those treated exclusively with antibiotics. We also investigated the efficacy of serum IgA antibody against glycopeptidolipid (GPL) core antigen (GPL core antibody) to monitor disease activity and predict the recurrence of disease after adjuvant lung resection. Methods We retrospectively evaluated the clinical characteristics and surgical outcomes of 35 patients surgically treated for NTM-PD. Furthermore, we compared surgically treated patients and control patients treated exclusively with antibiotics who were matched statistically 1:1 using a propensity score calculated from age, sex, body mass index, and radiologic features of disease. Results In the surgically treated patients, the median age was 58 (interquartile range, 47–65) years and 65.7% were female. Twenty-eight patients had Mycobacterium avium complex. Operations comprised four pneumonectomies, two bilobectomies, one bilobectomy plus segmentectomy, 17 lobectomies, two segmentectomies, and nine lobectomies plus segmentectomies. Postoperative complications occurred in seven patients (20%), there were no operative deaths, and 33 (94.3%) patients achieved negative sputum culture conversion. Refractory and recurrent cases were associated with remnant bronchiectasis, contralateral shadows, and positive acid-fast bacilli staining or culture. Of 28 statistically matched pairs, long-term sustained negative culture conversion was observed in 23 (82.2%) surgical group patients and in 14 (50.0%) non-surgical group patients (0.0438). The mortality rate was lower in the surgical group, but did not reach statistical significance (one in the surgical group and four in the non-surgical group, p = 0.3516). GPL core antibody was correlated with disease activity and recurrence. Conclusions NTM-PD patients who underwent adjuvant lung resection experienced overall favorable outcomes and achieved sputum culture conversion more frequently. Long-term mortality may have been reduced by this procedure, and the level of GPL core antibody was shown to be a good clinical indicator of disease activity after surgery.
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- 2020
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3. Role of tyramine in calcium dynamics of GABAergic neurons and escape behavior in Caenorhabditis elegans
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Yuko Kagawa-Nagamura, Keiko Gengyo-Ando, Masamichi Ohkura, and Junichi Nakai
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Caenorhabditis elegans ,Tyramine ,Calcium imaging ,Neuromodulation ,Escape behavior ,Zoology ,QL1-991 - Abstract
Abstract Background Tyramine, known as a “trace amine” in mammals, modulates a wide range of behavior in invertebrates; however, the underlying cellular and circuit mechanisms are not well understood. In the nematode Caenorhabditis elegans (C. elegans), tyramine affects key behaviors, including foraging, feeding, and escape responses. The touch-evoked backward escape response is often coupled with a sharp omega turn that allows the animal to navigate away in the opposite direction. Previous studies have showed that a metabotropic tyramine receptor, SER-2, in GABAergic body motor neurons controls deep body bending in omega turns. In this study, we focused on the role of tyramine in GABAergic head motor neurons. Our goal is to understand the mechanism by which tyraminergic signaling alters neural circuit activity to control escape behavior. Results Using calcium imaging in freely moving C. elegans, we found that GABAergic RME motor neurons in the head had high calcium levels during forward locomotion but low calcium levels during spontaneous and evoked backward locomotion. This calcium decrease was also observed during the omega turn. Mutant analyses showed that tbh-1 mutants lacking only octopamine had normal calcium responses, whereas tdc-1 mutants lacking both tyramine and octopamine did not exhibit the calcium decrease in RME. This neuromodulation was mediated by SER-2. Moreover, tyraminergic RIM neuron activity was negatively correlated with RME activity in the directional switch from forward to backward locomotion. These results indicate that tyramine released from RIM inhibits RME via SER-2 signaling. The omega turn is initiated by a sharp head bend when the animal reinitiates forward movement. Interestingly, ser-2 mutants exhibited shallow head bends and often failed to execute deep-angle omega turns. The behavioral defect and the abnormal calcium response in ser-2 mutants could be rescued by SER-2 expression in RME. These results suggest that tyraminergic inhibition of RME is involved in the control of omega turns. Conclusion We demonstrate that endogenous tyramine downregulates calcium levels in GABAergic RME motor neurons in the head via the tyramine receptor SER-2 during backward locomotion and omega turns. Our data suggest that this neuromodulation allows deep head bending during omega turns and plays a role in the escape behavior in C. elegans.
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- 2018
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4. Genetically encoded green fluorescent Ca2+ indicators with improved detectability for neuronal Ca2+ signals.
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Masamichi Ohkura, Takuya Sasaki, Junko Sadakari, Keiko Gengyo-Ando, Yuko Kagawa-Nagamura, Chiaki Kobayashi, Yuji Ikegaya, and Junichi Nakai
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Medicine ,Science - Abstract
Imaging the activities of individual neurons with genetically encoded Ca(2+) indicators (GECIs) is a promising method for understanding neuronal network functions. Here, we report GECIs with improved neuronal Ca(2+) signal detectability, termed G-CaMP6 and G-CaMP8. Compared to a series of existing G-CaMPs, G-CaMP6 showed fairly high sensitivity and rapid kinetics, both of which are suitable properties for detecting subtle and fast neuronal activities. G-CaMP8 showed a greater signal (F(max)/F(min) = 38) than G-CaMP6 and demonstrated kinetics similar to those of G-CaMP6. Both GECIs could detect individual spikes from pyramidal neurons of cultured hippocampal slices or acute cortical slices with 100% detection rates, demonstrating their superior performance to existing GECIs. Because G-CaMP6 showed a higher sensitivity and brighter baseline fluorescence than G-CaMP8 in a cellular environment, we applied G-CaMP6 for Ca(2+) imaging of dendritic spines, the putative postsynaptic sites. By expressing a G-CaMP6-actin fusion protein for the spines in hippocampal CA3 pyramidal neurons and electrically stimulating the granule cells of the dentate gyrus, which innervate CA3 pyramidal neurons, we found that sub-threshold stimulation triggered small Ca(2+) responses in a limited number of spines with a low response rate in active spines, whereas supra-threshold stimulation triggered large fluorescence responses in virtually all of the spines with a 100% activity rate.
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- 2012
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5. Benign metastasizing leiomyoma found as bilateral multiple lung nodules: A case report
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Kotaro Kawagishi, Yukiyasu Takeuchi, Satoshi Kawanaka, Yuya Kogita, Yuko Kagawa, and Meinoshin Okumura
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- 2022
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6. Two cases of gallbladder metastasis of lung cancer
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Yuko Kagawa, Yuya Kogita, Kotaro Kawagishi, Akio Hayashi, Koji Urasaki, and Yukiyasu Takeuchi
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- 2022
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7. A new platform for long-term tracking and recording of neural activity and simultaneous optogenetic control in freely behaving Caenorhabditis elegans
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Masamichi Ohkura, Keiko Gengyo-Ando, Junichi Nakai, Xianfeng Fei, Koichi Hashimoto, Yuko Kagawa-Nagamura, and Min Chen
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0301 basic medicine ,Light ,Nerve net ,Computer science ,Confocal ,Green Fluorescent Proteins ,Channelrhodopsin ,Optogenetics ,Tracking (particle physics) ,Animals, Genetically Modified ,03 medical and health sciences ,Channelrhodopsins ,medicine ,Biological neural network ,Animals ,Wakefulness ,Caenorhabditis elegans ,Caenorhabditis elegans Proteins ,Automation, Laboratory ,Neurons ,biology ,business.industry ,General Neuroscience ,Tracking system ,biology.organism_classification ,030104 developmental biology ,medicine.anatomical_structure ,Calcium ,Nerve Net ,business ,Neuroscience - Abstract
Background Real-time recording and manipulation of neural activity in freely behaving animals can greatly advance our understanding of how neural circuits regulate behavior. Ca 2+ imaging and optogenetic manipulation with optical probes are key technologies for this purpose. However, integrating the two optical approaches with behavioral analysis has been technically challenging. New method Here, we developed a new imaging system, ICaST ( I ntegrated platform for Ca 2+ imaging, S timulation, and T racking), which combines an automatic worm tracking system and a fast-scanning laser confocal microscope, to image neurons of interest in freely behaving C. elegans. We optimized different excitation wavelengths for the concurrent use of channelrhodopsin-2 and G-CaMP, a green fluorescent protein (GFP)-based, genetically encoded Ca 2+ indicator. Results Using ICaST in conjunction with an improved G-CaMP7, we successfully achieved long-term tracking and Ca 2+ imaging of the AVA backward command interneurons while tracking the head of a moving animal. We also performed all-optical manipulation and simultaneous recording of Ca 2+ dynamics from GABAergic motor neurons in conjunction with behavior monitoring. Comparison with existing method(s) Our system differs from conventional systems in that it does not require fluorescent markers for tracking and can track any part of the worm’s body via bright-field imaging at high magnification. Consequently, this approach enables the long-term imaging of activity from neurons or nerve processes of interest with high spatiotemporal resolution. Conclusion Our imaging system is a powerful tool for studying the neural circuit mechanisms of C. elegans behavior and has potential for use in other small animals.
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- 2017
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8. Distinct roles of the two VPS33 proteins in the endolysosomal system inCaenorhabditis elegans
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Sawako Yoshina, Junichi Nakai, Shohei Mitani, Keiko Gengyo-Ando, Muneyoshi Otori, Eriko Kage-Nakadai, and Yuko Kagawa-Nagamura
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0301 basic medicine ,biology ,Endosome ,Protein subunit ,Endocytic cycle ,macromolecular substances ,Cell Biology ,Vacuole ,Endocytosis ,biology.organism_classification ,medicine.disease_cause ,Biochemistry ,Cell biology ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Structural Biology ,Protein targeting ,Organelle ,Genetics ,medicine ,Molecular Biology ,030217 neurology & neurosurgery ,Caenorhabditis elegans - Abstract
Sec1/Munc-18 (SM) family proteins are essential regulators in intracellular transport in eukaryotic cells. The SM protein Vps33 functions as a core subunit of two tethering complexes, class C core vacuole/endosome tethering (CORVET) and homotypic fusion and vacuole protein sorting (HOPS) in the endocytic pathway in yeast. Metazoan cells possess two Vps33 proteins, VPS33A and VPS33B, but their precise roles remain unknown. Here, we present a comparative analysis of Caenorhabditis elegans null mutants for these proteins. We found that the vps-33.1 (VPS33A) mutants exhibited severe defects in both endocytic function and endolysosomal biogenesis in scavenger cells. Furthermore, vps-33.1 mutations caused endocytosis defects in other tissues, and the loss of maternal and zygotic VPS-33.1 resulted in embryonic lethality. By contrast, vps-33.2 mutants were viable but sterile, with terminally arrested spermatocytes. The spermatogenesis phenotype suggests that VPS33.2 is involved in the formation of a sperm-specific organelle. The endocytosis defect in the vps-33.1 mutant was not restored by the expression of VPS-33.2, which indicates that these proteins have nonredundant functions. Together, our data suggest that VPS-33.1 shares most of the general functions of yeast Vps33 in terms of tethering complexes in the endolysosomal system, whereas VPS-33.2 has tissue/organelle specific functions in C. elegans.
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- 2016
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9. Treatment strategy for empyema with fistulas
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Yuya Kogita, Yukiyasu Takeuchi, Meinoshin Okumura, Yuko Kagawa, and Akio Hayashi
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medicine.medical_specialty ,business.industry ,Medicine ,Treatment strategy ,business ,medicine.disease ,Empyema ,Surgery - Published
- 2020
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10. A 58 years old man of left tuberculous empyema with fistulas underwent open-wound thoracotomy six months ago. First, latissimus dorsal muscle was meticulously dissected for a flap. Next, pleural cavity was derided and short length of both lower ribs’ ends were removed for thoracoplasty. After omental flap was prepared, fistulas were closed by suturing with omental flap. Moreover latissimus dorsi muscle flap was tied over and the wound was closed without residual empyema space
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Yukiyasu Takeuchi, Akio Hayashi, Yuko Kagawa, Yuya Kogita, and Meinoshin Okumura
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Materials Chemistry - Published
- 2020
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11. An EWS is able to be carried to the aimed bronchus easily by attached to a tip of a curettage
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Yuko Kagawa, Meinoshin Okumura, Yukiyasu Takeuchi, Akio Hayashi, and Yuya Kogita
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Bronchus ,medicine.medical_specialty ,medicine.anatomical_structure ,business.industry ,medicine.medical_treatment ,Materials Chemistry ,medicine ,business ,Curettage ,Surgery - Published
- 2020
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12. Distinct roles of the two VPS33 proteins in the endolysosomal system in Caenorhabditis elegans
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Keiko, Gengyo-Ando, Eriko, Kage-Nakadai, Sawako, Yoshina, Muneyoshi, Otori, Yuko, Kagawa-Nagamura, Junichi, Nakai, and Shohei, Mitani
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Male ,Microscopy, Confocal ,Vesicular Transport Proteins ,Endosomes ,Spermatozoa ,Endocytosis ,Animals, Genetically Modified ,Protein Transport ,Mutation ,Oocytes ,Animals ,Caenorhabditis elegans ,Caenorhabditis elegans Proteins ,Lysosomes ,Spermatogenesis - Abstract
Sec1/Munc-18 (SM) family proteins are essential regulators in intracellular transport in eukaryotic cells. The SM protein Vps33 functions as a core subunit of two tethering complexes, class C core vacuole/endosome tethering (CORVET) and homotypic fusion and vacuole protein sorting (HOPS) in the endocytic pathway in yeast. Metazoan cells possess two Vps33 proteins, VPS33A and VPS33B, but their precise roles remain unknown. Here, we present a comparative analysis of Caenorhabditis elegans null mutants for these proteins. We found that the vps-33.1 (VPS33A) mutants exhibited severe defects in both endocytic function and endolysosomal biogenesis in scavenger cells. Furthermore, vps-33.1 mutations caused endocytosis defects in other tissues, and the loss of maternal and zygotic VPS-33.1 resulted in embryonic lethality. By contrast, vps-33.2 mutants were viable but sterile, with terminally arrested spermatocytes. The spermatogenesis phenotype suggests that VPS33.2 is involved in the formation of a sperm-specific organelle. The endocytosis defect in the vps-33.1 mutant was not restored by the expression of VPS-33.2, which indicates that these proteins have nonredundant functions. Together, our data suggest that VPS-33.1 shares most of the general functions of yeast Vps33 in terms of tethering complexes in the endolysosomal system, whereas VPS-33.2 has tissue/organelle specific functions in C. elegans.
- Published
- 2015
13. Genetically encoded green fluorescent Ca2+ indicators with improved detectability for neuronal Ca2+ signals
- Author
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Junko Sadakari, Takuya Sasaki, Keiko Gengyo-Ando, Masamichi Ohkura, Junichi Nakai, Chiaki Kobayashi, Yuko Kagawa-Nagamura, and Yuji Ikegaya
- Subjects
Fluorescence-lifetime imaging microscopy ,Anatomy and Physiology ,Dendritic spine ,Science ,Dendritic Spines ,Green Fluorescent Proteins ,Neuroimaging ,Stimulation ,Hippocampal formation ,Biology ,Neurological System ,Neurological Signaling ,Postsynaptic potential ,Molecular Cell Biology ,Biological neural network ,Animals ,Humans ,Calcium Signaling ,Cells, Cultured ,Calcium signaling ,Computational Neuroscience ,Neurons ,Multidisciplinary ,Dentate gyrus ,Pyramidal Cells ,Computational Biology ,Anatomy ,Signaling in Selected Disciplines ,Calcium Imaging ,Single Neuron Function ,Rats ,Neuroanatomical Tract-Tracing Techniques ,Neuroanatomy ,Neurology ,Dentate Gyrus ,Biophysics ,Medicine ,Calcium ,Indicators and Reagents ,Cellular Types ,Molecular Neuroscience ,Research Article ,Signal Transduction ,Neuroscience ,HeLa Cells - Abstract
Imaging the activities of individual neurons with genetically encoded Ca(2+) indicators (GECIs) is a promising method for understanding neuronal network functions. Here, we report GECIs with improved neuronal Ca(2+) signal detectability, termed G-CaMP6 and G-CaMP8. Compared to a series of existing G-CaMPs, G-CaMP6 showed fairly high sensitivity and rapid kinetics, both of which are suitable properties for detecting subtle and fast neuronal activities. G-CaMP8 showed a greater signal (F(max)/F(min) = 38) than G-CaMP6 and demonstrated kinetics similar to those of G-CaMP6. Both GECIs could detect individual spikes from pyramidal neurons of cultured hippocampal slices or acute cortical slices with 100% detection rates, demonstrating their superior performance to existing GECIs. Because G-CaMP6 showed a higher sensitivity and brighter baseline fluorescence than G-CaMP8 in a cellular environment, we applied G-CaMP6 for Ca(2+) imaging of dendritic spines, the putative postsynaptic sites. By expressing a G-CaMP6-actin fusion protein for the spines in hippocampal CA3 pyramidal neurons and electrically stimulating the granule cells of the dentate gyrus, which innervate CA3 pyramidal neurons, we found that sub-threshold stimulation triggered small Ca(2+) responses in a limited number of spines with a low response rate in active spines, whereas supra-threshold stimulation triggered large fluorescence responses in virtually all of the spines with a 100% activity rate.
- Published
- 2012
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