Interactions between interferon gamma, tumour necrosis factor alpha, and interleukin-1 in modulating progesterone and oestradiol production by human luteinized granulosa cells in culture

Hum Reprod. 1992 Nov;7(10):1361-4. doi: 10.1093/oxfordjournals.humrep.a137574.

Abstract

We have reported that the cytokines, interleukin-1 (IL-1), tumour necrosis factor alpha (TNF alpha), and interferon (IFN) alpha, beta, and gamma modulate the steroidogenic function of human luteinized granulosa cells in culture. In the present study we examined the interactions between these cytokines in modulating progesterone and oestradiol production by these cells. Neither IL-1 nor TNF alpha had significant effects on human chorionic gonadotrophin (HCG)-stimulated progesterone production, whereas IFN gamma (1-10 ng/ml) significantly reduced HCG-stimulated progesterone production by 26-37%. Concomitant treatment with IL-1 (1 ng/ml) did not further enhance the inhibitory effect of IFN gamma on HCG-stimulated progesterone production. In contrast, the combination of TNF alpha (1 ng/ml) and IFN gamma (10 ng/ml) acted synergistically to markedly inhibit HCG-stimulated progesterone production by 81%. In addition, IL-1 and TNF alpha, neither of which was effective alone, acted synergistically to reduce significantly HCG-stimulated progesterone production by 30%. The combination of TNF alpha and IFN gamma also markedly inhibited follicle stimulating hormone (FSH)-stimulated oestradiol production by 97%, a significantly greater inhibition than that obtained with either cytokine alone. These results suggest that the cytokines may interact to modulate the steroidogenic function of luteal cells in the developing corpus luteum.

MeSH terms

  • Analysis of Variance
  • Cells, Cultured
  • Chorionic Gonadotropin
  • Cytokines / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Estradiol / biosynthesis*
  • Female
  • Follicle Stimulating Hormone
  • Granulosa Cells / metabolism*
  • Humans
  • Interferon-gamma / pharmacology
  • Interleukin-1 / pharmacology
  • Luteal Phase / metabolism*
  • Progesterone / biosynthesis*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Chorionic Gonadotropin
  • Cytokines
  • Interleukin-1
  • Tumor Necrosis Factor-alpha
  • Progesterone
  • Estradiol
  • Interferon-gamma
  • Follicle Stimulating Hormone