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本帖最后由 bobo 于 2009-6-28 08:34 编辑 0 s8 B4 ]/ n$ z7 Z
0 s. Z& D4 Q, W4 T8 a7 c表观遗传学与干细胞——2009年亚洲生物高峰论坛录制(音频mp3)
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Hongkui Deng4 |! a, [+ x2 C. o( E4 ~2 n+ t8 ?! h
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Laboratory of Stem Cell and Generative Biology, College of Life Sciences, Peking University, Beijing 100871, China.: o; {8 g/ {) q1 k! ]2 L- L
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Human pluripotent stem cells represent a potentially unlimited source of functional pancreatic endocrine lineage cells. We established a new highly efficient approach to induce human embryonic stem (ES) cells and induced pluripotent stem (iPS) cells to differentiate into mature insulin-producing cells in a chemical-defined culture system. The differentiated cells obtained by this approach comprised nearly 25% insulin-positive cells as assayed by flow cytometry analysis, which released insulin/C-peptide in response to glucose stimuli in a manner comparable to that of adult human islets. Most of these insulin-producing cells co-expressed mature beta cell-specific markers such as NKX6-1 and PDX1, indicating a similar gene expression pattern to adult islet beta cells in vivo. This work provides a new model to study the mechanism of human pancreatic specialization and maturation in vitro, and enhances the possibility of utilizing patient-specific iPS cells for the treatment of diabetes
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