A small molecule that directs differentiation of human ESCs into the pancreatic lineage

被引:365
作者
Chen, Shuibing [1 ]
Borowiak, Malgorzata [1 ]
Fox, Julia L. [1 ]
Maehr, Rene [1 ]
Osafune, Kenji [1 ]
Davidow, Lance [1 ]
Lam, Kelvin [1 ]
Peng, Lee F. [2 ]
Schreiber, Stuart L. [2 ]
Rubin, Lee L. [1 ]
Melton, Douglas [1 ]
机构
[1] Harvard Stem Cell Inst, Dept Stem Cell & Regenerat Biol, Cambridge, MA USA
[2] Harvard Univ, Howard Hughes Med Inst, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
关键词
PROTEIN-KINASE-C; EMBRYONIC STEM-CELLS; TRANS-RETINOIC ACID; DEFINITIVE ENDODERM; EXPRESSION; MOUSE; HEDGEHOG; (-)-INDOLACTAM-V; SPECIFICATION; INHIBITION;
D O I
10.1038/nchembio.154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stepwise differentiation from embryonic stem cells (ESCs) to functional insulin-secreting beta cells will identify key steps in beta-cell development and may yet prove useful for transplantation therapy for diabetics. An essential step in this schema is the generation of pancreatic progenitors-cells that express Pdx1 and produce all the cell types of the pancreas. High-content chemical screening identified a small molecule, (-)-indolactam V, that induces differentiation of a substantial number of Pdx1-expressing cells from human ESCs. The Pdx1-expressing cells express other pancreatic markers and contribute to endocrine, exocrine and duct cells, in vitro and in vivo. Further analyses showed that (-)-indolactam V works specifically at one stage of pancreatic development, inducing pancreatic progenitors from definitive endoderm. This study describes a chemical screening platform to investigate human ESC differentiation and demonstrates the generation of a cell population that is a key milepost on the path to making beta cells.
引用
收藏
页码:258 / 265
页数:8
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