Progesterone-receptor antagonists and statins decrease de novo cholesterol synthesis and increase apoptosis in rat and human periovulatory granulosa cells in vitro

Biol Reprod. 2005 Mar;72(3):538-45. doi: 10.1095/biolreprod.104.033878. Epub 2004 Sep 22.

Abstract

Progesterone-receptor (PR) stimulation promotes survival in rat and human periovulatory granulosa cells. To investigate the mechanisms involved, periovulatory rat granulosa cells were incubated in vitro with or without the PR-antagonist Org 31710. Org 31710 caused the expected increase in apoptosis, and expression profiling using cDNA microarray analysis revealed regulation of several groups of genes with functional and/or metabolic connections. This regulation included decreased expression of genes involved in follicular rupture, increased stress responses, decreased angiogenesis, and decreased cholesterol synthesis. A decreased cholesterol synthesis was verified in experiments with both rat and human periovulatory granulosa cells treated with the PR-antagonists Org 31710 or RU 486 by measuring incorporation of [14C]acetate into cholesterol, cholesterol ester, and progesterone. Correspondingly, specific inhibition of cholesterol synthesis in periovulatory rat granulosa cells using 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors (lovastatin, mevastatin, or simvastatin) increased apoptosis, measured as DNA fragmentation and caspase-3/7 activity. The increase in apoptosis caused by simvastatin was reversed by addition of the cholesterol synthesis-intermediary mevalonic acid. These results show that PR antagonists reduce cholesterol synthesis in periovulatory granulosa cells and that cholesterol synthesis is important for granulosa cell survival.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology*
  • Cell Survival / physiology
  • Cholesterol / biosynthesis*
  • Estrenes / pharmacology
  • Female
  • Furans / pharmacology
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Granulosa Cells / drug effects
  • Granulosa Cells / metabolism*
  • Hormone Antagonists / pharmacology
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • In Vitro Techniques
  • Mifepristone / pharmacology
  • Oligonucleotide Array Sequence Analysis
  • Ovulation / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Progesterone / antagonists & inhibitors
  • Receptors, Progesterone / metabolism*
  • Signal Transduction / physiology

Substances

  • Estrenes
  • Furans
  • Hormone Antagonists
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Receptors, Progesterone
  • Org 31710
  • Mifepristone
  • Cholesterol