Effect of summer heat stress on gene expression in bovine uterine endometrial tissues

Anim Sci J. 2020 Jan-Dec;91(1):e13474. doi: 10.1111/asj.13474.

Abstract

Heat stress negatively affects reproductive functions in cows. Increased temperature disturbs fetal development in utero. However, the effect of heat stress on uterine endometrial tissues has not been fully examined. Using qPCR analysis, we measured the mRNA expression of various molecular markers in uterine endometrial tissue of dairy cows from Hokkaido, Japan, in winter and summer. Markers examined were heat shock proteins (HSPs), antioxidant enzymes (catalase, copper/zinc superoxide dismutase, manganese superoxide dismutase, and glutathione peroxidase 4), inflammatory cytokines, and interferon stimulated genes. Our results showed heat stress, body and milk temperatures were higher during summer than during winter. Expression levels of HSP27, HSP60, and HSP90 mRNA, and of catalase and copper/zinc superoxide dismutase mRNA were lower in summer than in winter. Tumor necrosis factor alpha expression was higher in summer than in winter. In conclusion, summer heat stress may reduce the expression of HSPs, affecting the levels of inflammatory cytokines in bovine uterine endometrial tissue.

Keywords: cow; heat stress; uterine endometrial tissue.

MeSH terms

  • Animals
  • Catalase / genetics*
  • Catalase / metabolism*
  • Cattle / genetics*
  • Cattle / physiology*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Endometrium / metabolism*
  • Extreme Heat*
  • Female
  • Fetal Development / genetics
  • Fetal Development / physiology
  • Gene Expression / genetics*
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / metabolism*
  • Heat-Shock Response / genetics*
  • Inflammation Mediators / metabolism
  • Metalloproteins / genetics
  • Metalloproteins / metabolism
  • RNA / genetics*
  • RNA / metabolism*
  • Reproduction
  • Seasons*
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Uterus / metabolism*

Substances

  • Cytokines
  • Heat-Shock Proteins
  • Inflammation Mediators
  • Metalloproteins
  • Tumor Necrosis Factor-alpha
  • RNA
  • Catalase
  • orgotein