Nasir Irem, Kedees Mamdouh H, Ehrlich Michelle E, Teitelman Gladys
Department of Anatomy and Cell Biology, SUNY-Downstate, Room 2-94, 450 Clarkson Avenue, Brooklyn, NY 11203, USA.
Mol Cell Endocrinol. 2005 Apr 15;233(1-2):1-13. doi: 10.1016/j.mce.2005.02.001.
During pregnancy, pancreatic beta cells undergo changes that are probably due to an increase in the lactogenic hormones prolactin (PRL) and placental lactogen (PL). Since the transcription factor PDX-1 is involved in the regulation of the beta cell function and phenotype, we tested the possibility that the effect of PRL on beta cells was mediated by PDX-1. Exposure of islet cells to PRL in vitro resulted in increased levels of PDX-1 protein and mRNA and a stimulation of pdx-1 transcription. However, PDX-1 levels in islets exposed in vivo to high concentration of prolactin was similar to controls. In vitro studies suggested that the up-regulation of PDX-1 by PRL was opposed by glucocorticoids (GC) at concentrations similar to those present in pregnant and control female mice. We conclude that, although pdx-1 is a key regulator of beta cell specific genes, it does not appear to play a central role in the up-regulation of islet cell function during pregnancy.
在怀孕期间,胰腺β细胞会发生变化,这可能是由于生乳激素催乳素(PRL)和胎盘催乳素(PL)水平升高所致。由于转录因子PDX-1参与β细胞功能和表型的调节,我们测试了PRL对β细胞的作用是否由PDX-1介导。体外将胰岛细胞暴露于PRL会导致PDX-1蛋白和mRNA水平升高,并刺激pdx-1转录。然而,体内暴露于高浓度催乳素的胰岛中PDX-1水平与对照组相似。体外研究表明,在与怀孕和对照雌性小鼠体内相似的糖皮质激素(GC)浓度下,PRL对PDX-1的上调作用受到抑制。我们得出结论,尽管pdx-1是β细胞特异性基因的关键调节因子,但它似乎在怀孕期间胰岛细胞功能的上调中并不起核心作用。