Role of tumor necrosis factor-α, interferon-γ and Fas-ligand on in vitro nitric oxide activity in the corpus luteum

Cytokine. 2013 Oct;64(1):18-21. doi: 10.1016/j.cyto.2013.07.015. Epub 2013 Aug 12.

Abstract

Normal reproductive function involves the expression of inflammatory mediators. Regarding the corpus luteum (CL), cytokines promote the cross-talk between immune, vascular and steroidogenic cells, among others. Moreover, TNF, IFNG and FASL were shown to regulate equine CL establishment and regression. We hypothesized that cytokines action on equine CL may be mediated by nitric oxide (NO), through the regulation of endothelial NO synthase (eNOS) expression. TNF increased eNOS mRNA level and NO metabolite (nitrite) production during CL growth. Cytokines combined action (TNF+IFNG+FASL) promoted eNOS protein upregulation in mid-CL and nitrite production in mid and late-CL. However, in late-CL, TNF alone decreased nitrite secretion. These results indicate that in equine CL, cytokines TNF, IFNG and FASL regulate NO activity, via eNOS expression modulation.

Keywords: Corpus luteum; Fas-ligand; IFN-γ; Nitric oxide; TNF-α.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Corpus Luteum / enzymology
  • Corpus Luteum / growth & development
  • Corpus Luteum / metabolism*
  • Fas Ligand Protein / metabolism*
  • Female
  • Horses
  • Interferon-gamma / metabolism*
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase Type III / genetics
  • Nitric Oxide Synthase Type III / metabolism
  • Nitrites / metabolism
  • RNA, Messenger / biosynthesis
  • Tumor Necrosis Factor-alpha / metabolism*
  • Up-Regulation

Substances

  • Fas Ligand Protein
  • Nitrites
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Interferon-gamma
  • Nitric Oxide Synthase Type III