McGrath Patrick S, Watson Carey L, Ingram Cameron, Helmrath Michael A, Wells James M
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH Department of General Surgery, University of Cincinnati, Cincinnati, OH.
Diabetes. 2015 Jul;64(7):2497-505. doi: 10.2337/db14-1412. Epub 2015 Feb 3.
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.
神经生成素3(NEUROG3)是小鼠内分泌胰腺发育所需的一种碱性螺旋-环-螺旋转录因子。相比之下,携带NEUROG3突变的人类出生时具有内分泌胰腺功能,这使人质疑NEUROG3是否是人类内分泌胰腺发育所必需的。为了直接验证这一点,我们利用CRISPR/Cas9介导的基因靶向技术构建了NEUROG3两个等位基因均被破坏的人类胚胎干细胞(hESC)系。NEUROG3(-/-)hESC系能有效形成胰腺祖细胞,但缺乏可检测到的NEUROG3蛋白,并且在体外不能形成内分泌细胞。此外,将PDX1(+)/NKX6.1(+)胰腺祖细胞植入小鼠后,NEUROG3(-/-)hESC系无法形成成熟的胰腺内分泌细胞。相比之下,NEUROG3敲低75%-90%会导致胰腺内分泌细胞发育减少,但不会使其缺失。我们得出结论,NEUROG3对人类内分泌胰腺发育至关重要,并且低至10%的NEUROG3就足以形成胰腺内分泌细胞。