Low-molecular-weight inhibitors of cell differentiation enable efficient growth of mouse iPS cells under feeder-free conditions

• Published in: Cytotechnology (Dordrecht) Vol. 67; no. 2; pp. 191 - 197
• Main Authors: Donai, Kenichiro, Inagaki, Akane, So, Kyoung-Ha, Kuroda, Kengo, Sone, Hideko, Kobayashi, Masayuki, Nishimori, Katsuhiko, Fukuda, Tomokazu
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.03.2015; Springer Nature B.V
• Subjects: Adaptation; Amino acids; Antibiotics; Biochemistry; Biomedicine; Biotechnology; Cell culture; Cell differentiation; Cell growth; Cell lines; Cell proliferation; Chemistry; Chemistry and Materials Science; Cloning; Collagen; Embryo cells; Embryo fibroblasts; Kinases; Morphology; Oct-4 protein; Phosphatase; Pluripotency; Regenerative medicine; Stem cells; Technical Note; United States > US; Japan; Feeder-free; Low-molecular-weight compounds; Serum-free; Cell culture condition; Induced pluripotent stem cells
• ISSN: 0920-9069; 1573-0778
• DOI: 10.1007/s10616-013-9686-8

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.