Human and mouse adipose-derived cells support feeder-independent induction of pluripotent stem cells

Shigeki Sugii(Salk Institute for Biological Studies), Yasuyuki S. Kida(Salk Institute for Biological Studies), Teruhisa Kawamura(Salk Institute for Biological Studies), Jotaro Suzuki(Salk Institute for Biological Studies), Rita Vassena(Center of Regenerative Medicine in Barcelona), Yunqiang Yin(Salk Institute for Biological Studies), Margaret Lutz(Salk Institute for Biological Studies), W. Travis Berggren(Salk Institute for Biological Studies), Juan Carlos Izpisúa Belmonte(Salk Institute for Biological Studies), Ronald M. Evans(Salk Institute for Biological Studies)
Proceedings of the National Academy of Sciences
February 4, 2010
Cited by 176Open Access
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Abstract

Although adipose tissue is an expandable and readily attainable source of proliferating, multipotent stem cells, its potential for use in regenerative medicine has not been extensively explored. Here we report that adult human and mouse adipose-derived stem cells can be reprogrammed to induced pluripotent stem (iPS) cells with substantially higher efficiencies than those reported for human and mouse fibroblasts. Unexpectedly, both human and mouse iPS cells can be obtained in feeder-free conditions. We discovered that adipose-derived stem cells intrinsically express high levels of pluripotency factors such as basic FGF, TGFbeta, fibronectin, and vitronectin and can serve as feeders for both autologous and heterologous pluripotent cells. These results demonstrate a great potential for adipose-derived cells in regenerative therapeutics and as a model for studying the molecular mechanisms of feeder-free iPS generation and maintenance.


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