Tumor necrosis factor-alpha inhibits follicle-stimulating hormone-induced differentiation in cultured rat granulosa cells

Biochem Biophys Res Commun. 1989 Sep 15;163(2):1038-46. doi: 10.1016/0006-291x(89)92326-7.

Abstract

We have investigated the effects of TNF-alpha on FSH-induced LH receptor expression, cAMP and progesterone production in cultured rat granulosa cells. TNF-alpha (0.5-100 ng/ml) inhibits the stimulating action of FSH on LH receptor formation in a dose-dependent manner with an IC50 of 1 ng/ml and an almost complete suppression of LH receptor induction for 50-100 ng/ml TNF-alpha. The inhibitory effect of TNF-alpha is not due to variations in cell number or viability but rather to a reduction of the LH receptor content per cell with no change in binding affinity (KD = 0.8 x 10(-10)M). TNF-alpha also inhibits the FSH-induced cAMP production but at a lower extent, with a maximum reduction of 60% for 100 ng/ml TNF-alpha. Moreover, TNF-alpha impairs the LH receptor formation induced by forskolin, cholera toxin or 8-Bromo-cAMP, indicating that the cytokine also acts at a step distal to FSH receptor and to cAMP formation. Finally, TNF-alpha decreases dramatically the progesterone synthesis that is stimulated by FSH, with a reduction to undetectable levels on and after 10 ng/ml TNF-alpha. These results suggest that TNF-alpha may drastically reduce the capacity of granulosa cells to differentiate upon FSH stimulation and to respond to LH during the physiological ovarian follicular maturation. Such anti-gonadotropic action of TNF-alpha on granulosa cell differentiation may be also relevant to the alteration of ovarian function during physiopathological processes like inflammatory or infection diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Cholera Toxin / pharmacology
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Female
  • Follicle Stimulating Hormone / pharmacology*
  • Granulosa Cells / cytology
  • Granulosa Cells / metabolism*
  • In Vitro Techniques
  • Progesterone / antagonists & inhibitors
  • Rats
  • Receptors, Gonadotropin / drug effects
  • Receptors, Gonadotropin / metabolism
  • Receptors, LH / drug effects
  • Receptors, LH / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Receptors, Gonadotropin
  • Receptors, LH
  • Tumor Necrosis Factor-alpha
  • Colforsin
  • Progesterone
  • Follicle Stimulating Hormone
  • Cholera Toxin
  • Cyclic AMP