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H1foo Has a Pivotal Role in Qualifying Induced Pluripotent Stem Cells

Authors :
Akira Kunitomi
Shinsuke Yuasa
Fumihiro Sugiyama
Yuki Saito
Tomohisa Seki
Dai Kusumoto
Shin Kashimura
Makoto Takei
Shugo Tohyama
Hisayuki Hashimoto
Toru Egashira
Yoko Tanimoto
Saori Mizuno
Shoma Tanaka
Hironobu Okuno
Kazuki Yamazawa
Hideo Watanabe
Mayumi Oda
Ruri Kaneda
Yumi Matsuzaki
Toshihiro Nagai
Hideyuki Okano
Ken-ichi Yagami
Mamoru Tanaka
Keiichi Fukuda
Source :
Stem Cell Reports, Vol 6, Iss 6, Pp 825-833 (2016)
Publication Year :
2016
Publisher :
Elsevier, 2016.

Abstract

Summary: Embryonic stem cells (ESCs) are a hallmark of ideal pluripotent stem cells. Epigenetic reprogramming of induced pluripotent stem cells (iPSCs) has not been fully accomplished. iPSC generation is similar to somatic cell nuclear transfer (SCNT) in oocytes, and this procedure can be used to generate ESCs (SCNT-ESCs), which suggests the contribution of oocyte-specific constituents. Here, we show that the mammalian oocyte-specific linker histone H1foo has beneficial effects on iPSC generation. Induction of H1foo with Oct4, Sox2, and Klf4 significantly enhanced the efficiency of iPSC generation. H1foo promoted in vitro differentiation characteristics with low heterogeneity in iPSCs. H1foo enhanced the generation of germline-competent chimeric mice from iPSCs in a manner similar to that for ESCs. These findings indicate that H1foo contributes to the generation of higher-quality iPSCs. : In this article, Yuasa and colleagues show that the mammalian oocyte-specific linker histone H1foo has beneficial effects on iPSC generation. Induction of H1foo with Oct4, Sox2, and Klf4 enhanced the efficiency of iPSC generation and improved the quality of iPSCs with low heterogeneity in vitro and in vivo. These findings indicate that H1foo contributes to the generation of higher quality iPSCs.

Details

Language :
English
ISSN :
22136711
Volume :
6
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Stem Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.bf963277fe834fbd80ee19703ff21102
Document Type :
article
Full Text :
https://doi.org/10.1016/j.stemcr.2016.04.015