Low-molecular-weight inhibitors of cell differentiation enable efficient growth of mouse iPS cells under feeder-free conditions
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  • 作者:Kenichiro Donai (1)
    Akane Inagaki (1)
    Kyoung-Ha So (1)
    Kengo Kuroda (1)
    Hideko Sone (2)
    Masayuki Kobayashi (3)
    Katsuhiko Nishimori (1)
    Tomokazu Fukuda (1)
  • 关键词:Induced pluripotent stem cells ; Cell culture condition ; Serum ; free ; Feeder ; free ; Low ; molecular ; weight compounds
  • 刊名:Cytotechnology
  • 出版年:2015
  • 出版时间:March 2015
  • 年:2015
  • 卷:67
  • 期:2
  • 页码:191-197
  • 全文大小:2,582 KB
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  • 作者单位:Kenichiro Donai (1)
    Akane Inagaki (1)
    Kyoung-Ha So (1)
    Kengo Kuroda (1)
    Hideko Sone (2)
    Masayuki Kobayashi (3)
    Katsuhiko Nishimori (1)
    Tomokazu Fukuda (1)

    1. Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-amamiyamachi, Aoba-ku, Sendai, 981-8555, Japan
    2. Environmental Exposure Research Section, Center for Environmental Risk Research, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki, 305-8506, Japan
    3. Graduate School of Bioresource Sciences, Akita Prefectural University, 241-438 Kaidobata-Nishi, Nakano, Shimoshinjo, Akita, 010-0195, Japan
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Biotechnology
    Biomedicine
    Biochemistry
  • 出版者:Springer Netherlands
  • ISSN:1573-0778
文摘
Embryonic stem cells and induced pluripotent stem (iPS) cells are usually maintained on feeder cells derived from mouse embryonic fibroblasts (MEFs). In recent years, the cell culture of iPS cells under serum- and feeder-free conditions is gaining attention in overcoming the biosafety issues for clinical applications. In this study, we report on the use of multiple small-molecular inhibitors (i.e., CHIR99021, PD0325901, and Thiazovivin) to efficiently cultivate mouse iPS cells without feeder cells in a chemically-defined and serum-free condition. In this condition, we showed that mouse iPS cells are expressing the Nanog, Oct3/4, and SSEA-1 pluripotent markers, indicating that the culture condition is optimized to maintain the pluripotent status of iPS cells. Without these small-molecular inhibitors, mouse iPS cells required the adaptation period to start the stable cell proliferation. The application of these inhibitors enabled us the shortcut culture method for the cellular adaptation. This study will be useful to efficiently establish mouse iPS cell lines without MEF-derived feeder cells.

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