Palgi J, Stumpf E, Otonkoski T
Transplantation Laboratory, Haartman Institute and the Hospital for Children and Adolescents, University of Helsinki, PO Box 21 (Haartmaninkatu 3), FIN-00014, Helsinki, Finland.
Mol Cell Endocrinol. 2000 Jul 25;165(1-2):41-9. doi: 10.1016/s0303-7207(00)00265-3.
AR42J is an exocrine pancreatic cell line that has been reported to differentiate towards an endocrine phenotype when stimulated with various growth factors, such as activin A, hepatocyte growth factor (HGF), betacellulin or glucagon-like peptide 1. In our experiments, AR42J-B13 cells differentiated morphologically in response to the growth factor treatment as reported previously. However, they failed to express the insulin gene. We found that the cells did not express several transcription factors known to be found in the beta-cell, including Nkx6.1, isl-1, Pax4 and Pax6. In addition, the mRNA level for pdx-1 and Nkx2.2 were very low in comparison to the insulinoma cell lines INS-1 and RINm5F. However, some transcription factors typically found in beta-cells and neuroendocrine cells were expressed also in the AR42J-B13 cells. These included BETA2/NeuroD, HNF1alpha, C/EBPbeta and IA-1. Unlike the insulinoma cells, AR42J cells expressed the exocrine transcription factor p48. In order to induce endocrine differentiation, we transfected the AR42J-B13 cells with the full length cDNAs of isl-1, Nkx6.1, Nkx2.2 and pdx-1 under the control of the CMV promoter, both separately and in combinations. The expression of Nkx2.2 led consistently to the appearance of pancreatic polypeptide but not insulin, glucagon or somatostatin mRNA. The PP mRNA expression in Nkx2.2 cDNA transfected cells was independent of the growth factor treatment used for differentiating AR42J cells. In conclusion, the AR42J-B13 line possesses some features of a pancreatic neuroendocrine cell. However, we were unable to confirm the capacity of these cells to differentiate into insulin-producing cells. Our results indicate that Nkx2.2 plays a role in the transcriptional regulation of PP expression.
AR42J是一种外分泌胰腺细胞系,据报道,当受到各种生长因子刺激时,如激活素A、肝细胞生长因子(HGF)、β细胞ulin或胰高血糖素样肽1,它会向内分泌表型分化。在我们的实验中,AR42J - B13细胞在生长因子处理下如先前报道的那样发生了形态学分化。然而,它们未能表达胰岛素基因。我们发现这些细胞不表达已知在β细胞中存在的几种转录因子,包括Nkx6.1、胰岛 - 1、Pax4和Pax6。此外,与胰岛素瘤细胞系INS - 1和RINm5F相比,pdx - 1和Nkx2.2的mRNA水平非常低。然而,一些通常在β细胞和神经内分泌细胞中发现的转录因子在AR42J - B13细胞中也有表达。这些包括BETA2 / NeuroD、HNF1α、C / EBPβ和IA - 1。与胰岛素瘤细胞不同,AR42J细胞表达外分泌转录因子p48。为了诱导内分泌分化,我们用CMV启动子控制下的isl - 1、Nkx6.1、Nkx2.2和pdx - 1的全长cDNA分别或组合转染AR42J - B13细胞。Nkx2.2的表达一致地导致了胰多肽的出现,但没有胰岛素、胰高血糖素或生长抑素mRNA的出现。Nkx2.2 cDNA转染细胞中PP mRNA的表达与用于分化AR42J细胞的生长因子处理无关。总之,AR42J - B13细胞系具有胰腺神经内分泌细胞的一些特征。然而,我们无法证实这些细胞分化为胰岛素产生细胞的能力。我们的结果表明Nkx2.2在PP表达的转录调控中起作用。