N-acetylcysteine modulates non-esterified fatty acid-induced pyroptosis and inflammation in granulosa cells

Mol Immunol. 2020 Nov:127:157-163. doi: 10.1016/j.molimm.2020.09.011. Epub 2020 Sep 25.

Abstract

In the perinatal period of dairy cows, negative energy balance (NEB) is likely to occur, which increases the level of non-esterified fatty acids (NEFA) in the follicular fluid, hinders the proliferation of granulosa cells (GCs), and thus endangers the development of oocytes and the fecundity of dairy cows. We found that there were oxidative stress and inflammatory response in the serum of cows with perinatal ketosis. Whether the oxidative stress induced by NEFA is involved in the pyroptosis and inflammation of GCs remains unclear. After NEFA treatment, the expression of NLRP3 and caspase-1 and the release of inflammatory cytokines IL-1β were increased in a dose-dependent manner, indicating that NEFA may contribute to pyroptosis. Besides, NEFA stimulation induced oxidative stress, resulting in the phosphorylation of NF-κB, and increased the production of interleukin (IL)-6 and nitric oxide (NO), indicating that NEFA may induce inflammation in GCs. However, the NEFA-mediated effects were observably reversed when the GCs were pre-treated with antioxidant and radical scavenger, N-acetylcysteine (NAC). Taken together, our results reveal that NEFA can induce pyroptosis and inflammation through NLRP3 inflammasome and TLR4/NF-κB pathway, respectively, and NAC can alleviate these conditions.

Keywords: Granulosa cells; N-acetylcysteine; NF-κB pathway; NLRP3 inflammasome; Oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / pharmacology*
  • Animals
  • Cattle
  • Cell Survival / drug effects
  • Fatty Acids, Nonesterified / toxicity*
  • Female
  • Granulosa Cells / drug effects
  • Granulosa Cells / pathology*
  • Inflammation / pathology*
  • Inflammation Mediators / metabolism
  • Ketosis / pathology
  • Models, Biological
  • Oxidation-Reduction / drug effects
  • Oxidative Stress / drug effects
  • Pyroptosis / drug effects*
  • Up-Regulation / drug effects

Substances

  • Fatty Acids, Nonesterified
  • Inflammation Mediators
  • Acetylcysteine