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.
Original language | English |
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Pages (from-to) | 1-13 |
Number of pages | 13 |
Journal | Molecular and Cellular Endocrinology |
Volume | 233 |
Issue number | 1-2 |
DOIs | |
State | Published - 15 Apr 2005 |
Externally published | Yes |
Keywords
- Glucocorticoids
- Insulin cells
- Pdx-1
- Pregnancy hormones
- Prolactin