Stimulation of steroidogenesis in immature rat Leydig cells evoked by interleukin-1alpha is potentiated by growth hormone and insulin-like growth factors

Endocrinology. 2005 Jan;146(1):221-30. doi: 10.1210/en.2004-0485. Epub 2004 Oct 14.

Abstract

The cytokine IL-1alpha is produced constitutively by the intact testis, but its function in this organ remains largely unknown. In this study we examined cooperation between IL-1alpha and GH and IGFs with regard to stimulation of steroidogenesis by Leydig cells from 40-d-old rats in vitro. IL-1alpha alone stimulated testosterone (T) and dihydrotestosterone (DHT) production. GH, IGF-I, or IGF-II alone was without effect on T production, but they were found to elevate DHT release, albeit without an obvious dose-response effect. Costimulation with IL-1alpha and GH or with IL-1alpha and IGF-I or IGF-II elevated the rate of steroidogenesis (both T and DHT) above that observed with IL-1alpha alone. GH was found to increase the level of IGF-I in the cultured Leydig cells, an effect that was potentiated by IL-1alpha. The costimulatory effect of GH on steroidogenesis was abolished by treatment with picropodophyllin, a specific inhibitor of the IGF-I receptor, indicating that the action of GH is mediated via IGF-I. Moreover, cells costimulated with IL-1alpha and GH exhibited a marked decrease in the level of intact IGF-binding protein-3 in the culture medium due to the induction of proteolytic activity toward this binding protein. In contrast, secretion of IGF-binding protein-2 was increased by such costimulation. These findings suggest that the stimulation of steroidogenesis in Leydig cells evoked by GH and IGFs requires cooperation with IL-1alpha. This cooperation may play an important role in connection with postnatal Leydig cell maturation and steroidogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / biosynthesis*
  • Animals
  • Cell Division / drug effects
  • Cells, Cultured
  • Dihydrotestosterone / metabolism
  • Drug Synergism
  • Growth Hormone / pharmacology*
  • Insulin-Like Growth Factor Binding Proteins / metabolism
  • Insulin-Like Growth Factor I / pharmacology
  • Insulin-Like Growth Factor II / pharmacology
  • Interleukin-1 / pharmacology*
  • Leydig Cells / cytology
  • Leydig Cells / drug effects*
  • Leydig Cells / metabolism*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, IGF Type 1 / antagonists & inhibitors
  • Somatomedins / pharmacology*
  • Testosterone / metabolism

Substances

  • Androgens
  • Insulin-Like Growth Factor Binding Proteins
  • Interleukin-1
  • Somatomedins
  • Dihydrotestosterone
  • Testosterone
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II
  • Growth Hormone
  • Receptor, IGF Type 1