The Basic Helix-Loop-Helix Transcription Factor NEUROG3 Is Required for Development of the Human Endocrine Pancreas

被引:88
作者
McGrath, Patrick S. [1 ]
Watson, Carey L. [2 ,3 ]
Ingram, Cameron [1 ]
Helmrath, Michael A. [2 ,3 ]
Wells, James M. [1 ,4 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Dev Biol, Cincinnati, OH 45229 USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Pediat Gen & Thorac Surg, Cincinnati, OH 45229 USA
[3] Univ Cincinnati, Dept Gen Surg, Cincinnati, OH USA
[4] Cincinnati Childrens Hosp Med Ctr, Div Endocrinol, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
EMBRYONIC STEM-CELLS; BETA-CELL; DIFFERENTIATION; GENE; NEUROGENIN-3; PROGENITORS; EXPRESSION; SPECIFICATION; ENDODERM; PAX4;
D O I
10.2337/db14-1412
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neurogenin3 (NEUROG3) is a basic helix-loop-helix transcription factor required for development of the endocrine pancreas in mice. In contrast, humans with NEUROG3 mutations are born with endocrine pancreas function, calling into question whether NEUROG3 is required for human endocrine pancreas development. To test this directly, we generated human embryonic stem cell (hESC) lines where both alleles of NEUROG3 were disrupted using CRISPR/Cas9-mediated gene targeting. NEUROG3(-/-) hESC lines efficiently formed pancreatic progenitors but lacked detectible NEUROG3 protein and did not form endocrine cells in vitro. Moreover, NEUROG3(-/-) hESC lines were unable to form mature pancreatic endocrine cells after engraftment of PDX1(+)/NKX6.1(+) pancreatic progenitors into mice. In contrast, a 75-90% knockdown of NEUROG3 caused a reduction, but not a loss, of pancreatic endocrine cell development. We conclude that NEUROG3 is essential for endocrine pancreas development in humans and that as little as 10% NEUROG3 is sufficient for formation of pancreatic endocrine cells.
引用
收藏
页码:2497 / 2505
页数:9
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