Zhang Y Q, Mashima H, Kojima I
Department of Cell Biology, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Japan.
Diabetes. 2001 Feb;50 Suppl 1:S10-4. doi: 10.2337/diabetes.50.2007.s10.
Pancreatic AR42J cells possess both exocrine and neuroendocrine properties and convert to insulin-producing cells upon treatment with activin A and hepatocyte growth factor (HGF). We studied changes in the mRNA expression of various transcription factors during the course of differentiation. Among the transcription factors studied, expression levels of Pax4 and neurogenin3 changed significantly. These two factors were not detected in naive cells, whereas their mRNA levels were markedly increased after treatment with activin A and HGF. Thus, these two factors were induced by activin A. Transfection of Pax4 did not induce any changes in morphology or expression of pancreatic polypeptide (PP). Furthermore, introduction of antisense Pax4 did not affect the conversion into insulin-producing cells induced by activin A and HGF. In contrast, transfection of neurogenin3 induced morphological changes similar to those induced by activin A. In addition, transfection of neurogenin3 induced the expression of PP. Conversely, introduction of antisense neurogenin3 blocked the differentiation of AR42J cells induced by activin A and HGF. These results indicate that activin A regulates the expression of neurogenin3, which is critical for the differentiation of AR42J into endocrine cells.
胰腺AR42J细胞兼具外分泌和神经内分泌特性,在用激活素A和肝细胞生长因子(HGF)处理后可转化为胰岛素生成细胞。我们研究了分化过程中各种转录因子mRNA表达的变化。在所研究的转录因子中,Pax4和神经生成素3的表达水平变化显著。在未处理的细胞中未检测到这两种因子,而在用激活素A和HGF处理后它们的mRNA水平显著升高。因此,这两种因子是由激活素A诱导产生的。转染Pax4并未引起形态学或胰多肽(PP)表达的任何变化。此外,导入反义Pax4并不影响激活素A和HGF诱导的向胰岛素生成细胞的转化。相反,转染神经生成素3诱导出与激活素A诱导的相似的形态学变化。另外,转染神经生成素3诱导了PP的表达。相反,导入反义神经生成素3阻断了激活素A和HGF诱导的AR42J细胞的分化。这些结果表明,激活素A调节神经生成素3的表达,而神经生成素3对于AR42J细胞分化为内分泌细胞至关重要。