Interleukin-1 stimulates growth and inhibits progesterone secretion in cultures of porcine granulosa cells

Endocrinology. 1989 Feb;124(2):884-90. doi: 10.1210/endo-124-2-884.

Abstract

Interleukin-1 (IL-1) significantly inhibited basal progesterone secretion and influenced the cell number in high density cultures of porcine granulosa cells harvested from small (1-2 mm) or medium (3-5 mm) follicles. These two effects of IL-1 showed similar but inverse dose-response relationships: Significant effects were observed at concentrations higher than 50 pg/ml, and the maximal effective concentration was 5 ng/ml, which reduced progesterone secretion by 53.5 +/- 2.1%. In contrast, IL-1 neither inhibited progesterone secretion nor did it influence cell number in cultures of fully mature granulosa cells harvested from the largest (8-11 mm) follicles. The growth-promoting effect of IL-1 on granulosa cells was further examined in the low density cultures, which revealed that IL-1 significantly stimulated proliferation of the less mature granulosa cells at concentrations higher than 50 pg/ml, and that at a maximal stimulatory concentration (25 ng/ml) it increased cell number to 206 +/- 11% of control. Although IL-1 increased cell number and reduced progesterone secretion of fully mature granulosa cells after 5 days in low density cultures, it seemed that the proliferating population were not the cells with luteinized morphology and positive 3 beta-hydroxysteroid dehydrogenase staining. The proliferating population of cells appeared to have less mature morphology and were negative for 3 beta-hydroxysteroid dehydrogenase staining.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxysteroid Dehydrogenases / metabolism
  • Animals
  • Cell Division / drug effects
  • Cells, Cultured
  • Female
  • Granulosa Cells / cytology*
  • Granulosa Cells / drug effects
  • Granulosa Cells / enzymology
  • Granulosa Cells / metabolism
  • Interleukin-1 / pharmacology*
  • Kinetics
  • Progesterone / metabolism*
  • Recombinant Proteins / pharmacology*
  • Swine

Substances

  • Interleukin-1
  • Recombinant Proteins
  • Progesterone
  • 3-Hydroxysteroid Dehydrogenases