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Research Paper|Volume 11, Issue 15|pp 5535—5547

HO-1 reduces heat stress-induced apoptosis in bovine granulosa cells by suppressing oxidative stress

Yiru Wang1, Caixia Yang1, Nahla Abdalla Hassan Elsheikh1, Chengmin Li1, Fangxiao Yang1, Genlin Wang1, Lian Li1
  • 1College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China
Received: February 22, 2019Accepted: July 29, 2019Published: August 12, 2019

Copyright © 2019 Wang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Heat stress negatively affects reproduction in cattle by disrupting the normal function of ovarian granulosa cells (GCs), ultimately leading to oxidative damage and cell death via apoptosis. Heme oxygenase-1(HO-1) is a member of the heat shock protein family, which are associated with cellular antioxidant defenses and anti-apoptotic functions. Recent studies demonstrated that HO-1 is upregulated in heat-stressed cells. In the present study, we investigated the expression of HO-1 in bovine GCs transiently exposed to heat stress and characterized the expression and activity of key oxidative stress enzymes and molecules. We show that heat stress induced oxidative stress and apoptosis, and enhanced Nrf2 and HO-1 expression in primary GC cultures. Knocking down HO-1 expression using siRNA exacerbated both oxidative stress and apoptosis, whereas pre-treating GCs with hemin, which induces HO-1 expression, partially prevented these effects. These findings demonstrate that HO-1 attenuates heat stress-induced apoptosis in bovine GCs by decreasing production of reactive oxygen species and activating the antioxidant response.