Ogihara Takeshi, Fujitani Yoshio, Uchida Toyoyoshi, Kanno Rei, Choi Jong Bock, Hirose Takahisa, Kawamori Ryuzo, Watada Hirotaka
Department of Medicine, Metabolism and Endocrinology, Juntendo University School of Medicine, Tokyo, Japan.
Endocr J. 2008 Aug;55(4):691-8. doi: 10.1507/endocrj.k07e-169. Epub 2008 May 28.
Neurogenin 3 (Ngn3) is a transcription factor that regulates an initial step of differentiation from uncommitted pancreatic progenitors into endocrine cells. Additional transcription factors are required for complete differentiation into mature pancreatic beta cells. In this study, we established an in vitro model system of beta-cell differentiation by adenovirus-mediated expression of several transcription factors in AR42J-B13 cells, a pancreatic progenitor-like cell line derived from exocrine pancreas. Exogenous expression of Ngn3 in AR42J-B13 cells induced expression of Nkx2.2, Pax4, and Pax6, which are all essential for beta-cell differentiation in mouse embryos. However, Ngn3 did not induce more downstream regulators of beta-cell differentiation, Nkx6.1 and Maf A. Coexpression of Nkx6.1 and Ngn3 induced endogenous expression of the insulin 2 gene, while coexpression of Maf A and Ngn3 induced both insulin 1 and 2 genes in AR42J-B13 cells. Our data demonstrated that Ngn3 expressed together with Nkx6.1 or MafA induces AR42J-B13 cells to differentiate into insulin-producing cells, supporting the use of these cells as a model system for studying beta-cell differentiation in vitro.
神经生成素3(Ngn3)是一种转录因子,可调节未分化的胰腺祖细胞向内分泌细胞分化的初始步骤。完全分化为成熟的胰腺β细胞还需要其他转录因子。在本研究中,我们通过腺病毒介导的几种转录因子在AR42J-B13细胞(一种源自外分泌胰腺的胰腺祖细胞样细胞系)中的表达,建立了β细胞分化的体外模型系统。AR42J-B13细胞中外源表达Ngn3可诱导Nkx2.2、Pax4和Pax6的表达,这些都是小鼠胚胎中β细胞分化所必需的。然而,Ngn3并未诱导更多β细胞分化的下游调节因子Nkx6.1和Maf A。Nkx6.1和Ngn3共表达可诱导胰岛素2基因的内源性表达,而Maf A和Ngn3共表达可诱导AR42J-B13细胞中胰岛素1和2基因的表达。我们的数据表明,Ngn3与Nkx6.1或MafA共同表达可诱导AR42J-B13细胞分化为胰岛素产生细胞,支持将这些细胞用作体外研究β细胞分化的模型系统。