Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9915001 | Molecular and Cellular Endocrinology | 2005 | 13 Pages |
Abstract
During pregnancy, pancreatic β 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 β cell function and phenotype, we tested the possibility that the effect of PRL on β 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 β cell specific genes, it does not appear to play a central role in the up-regulation of islet cell function during pregnancy.
Keywords
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Cell Biology
Authors
Irem Nasir, Mamdouh H. Kedees, Michelle E. Ehrlich, Gladys Teitelman,