4.7 Article

A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells

Journal

SCIENTIFIC REPORTS
Volume 4, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/srep03594

Keywords

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Funding

  1. Leading Project of the Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  2. Funding Program for World-Leading Innovative Research and Development on Science and Technology (FIRST Program) of Japan Society for the Promotion of Science
  3. Japan Society for the Promotion of Science
  4. MEXT
  5. New Energy and Industrial Technology Development Organization (NEDO) of Japan
  6. Coordination, Support and Training Program for Translational Research of the Ministry of Education Culture, Sports, Science and Technology of Japan
  7. Grants-in-Aid for Scientific Research [24590353, 25860747, 24790277, 24592124] Funding Source: KAKEN

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In order to apply human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs) to regenerative medicine, the cells should be produced under restricted conditions conforming to GMP guidelines. Since the conventional culture system has some issues that need to be addressed to achieve this goal, we developed a novel culture system. We found that recombinant laminin-511 E8 fragments are useful matrices for maintaining hESCs and hiPSCs when used in combination with a completely xeno-free (Xf) medium, StemFit (TM). Using this system, hESCs and hiPSCs can be easily and stably passaged by dissociating the cells into single cells for long periods, without any karyotype abnormalities. Human iPSCs could be generated under feeder-free (Ff) and Xf culture systems from human primary fibroblasts and blood cells, and they possessed differentiation abilities. These results indicate that hiPSCs can be generated and maintained under this novel Ff and Xf culture system.

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