The ERK signaling cascade inhibits gonadotropin-stimulated steroidogenesis

J Biol Chem. 2001 Apr 27;276(17):13957-64. doi: 10.1074/jbc.M006852200. Epub 2001 Jan 22.

Abstract

The response of granulosa cells to luteinizing hormone (LH) and follicle-stimulating hormone (FSH) is mediated mainly by cAMP/protein kinase A (PKA) signaling. Notably, the activity of the extracellular signal-regulated kinase (ERK) signaling cascade is elevated in response to these stimuli as well. We studied the involvement of the ERK cascade in LH- and FSH-induced steroidogenesis in two granulosa-derived cell lines, rLHR-4 and rFSHR-17, respectively. We found that stimulation of these cells with the appropriate gonadotropin induced ERK activation as well as progesterone production downstream of PKA. Inhibition of ERK activity enhanced gonadotropin-stimulated progesterone production, which was correlated with increased expression of the steroidogenic acute regulatory protein (StAR), a key regulator of progesterone synthesis. Therefore, it is likely that gonadotropin-stimulated progesterone formation is regulated by a pathway that includes PKA and StAR, and this process is down-regulated by ERK, due to attenuation of StAR expression. Our results suggest that activation of PKA signaling by gonadotropins not only induces steroidogenesis but also activates down-regulation machinery involving the ERK cascade. The activation of ERK by gonadotropins as well as by other agents may be a key mechanism for the modulation of gonadotropin-induced steroidogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Retracted Publication

MeSH terms

  • Animals
  • Cell Line
  • Chorionic Gonadotropin / metabolism
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • Female
  • Flavonoids / pharmacology
  • Follicle Stimulating Hormone / metabolism
  • Gonadotropins / metabolism*
  • Granulosa Cells / metabolism
  • Humans
  • Luteinizing Hormone / metabolism
  • MAP Kinase Signaling System
  • Microscopy, Fluorescence
  • Mitogen-Activated Protein Kinases / metabolism*
  • Models, Biological
  • Phosphoproteins / biosynthesis
  • Phosphorylation
  • Plasmids / metabolism
  • Progesterone / biosynthesis
  • Progesterone / metabolism
  • Protein Binding
  • Rats
  • Signal Transduction*
  • Steroids / biosynthesis*
  • Time Factors
  • Transfection

Substances

  • Chorionic Gonadotropin
  • Enzyme Inhibitors
  • Flavonoids
  • Gonadotropins
  • Phosphoproteins
  • Steroids
  • steroidogenic acute regulatory protein
  • Colforsin
  • Progesterone
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinases
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one