Effects of lipopolysaccharide on maturation of bovine oocyte in vitro and its possible mechanisms
PDF | HTML | How to cite
Metrics: PDF 1774 views | HTML 2782 views | ?
Shan-Jiang Zhao1,*, Yun-Wei Pang1,*, Xue-Ming Zhao1, Wei-Hua Du1, Hai-Sheng Hao1, Hua-Bin Zhu1
1Embryo Biotechnology and Reproduction Laboratory, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China
*These authors contributed equally to this work
Hua-Bin Zhu, email: [email protected]
Keywords: lipopolysaccharide, oocyte, cytoskeleton, oxidative stress, epigenetic modifications
Received: September 24, 2016 Accepted: December 07, 2016 Published: December 16, 2016
Lipopolysaccharide disturbs the secretion of gonadotropin, endometrial function and implantation efficiency. However, there is little information regarding the effects of lipopolysaccharide on cyclic ovary activity, especially oocyte maturation. Therefore, we aimed to investigate the effects of lipopolysaccharide on the maturation potential of bovine oocytes. We found that lipopolysaccharide exposure significantly decreased the first polar body extrusion rate and delayed the cell cycle progression. The abnormal spindle rate was significantly increased in lipopolysaccharide treatment group, accompanied by disrupted localization and level of phosphorylated mitogen-activated protein kinase (p-MAPK). Moreover, lipopolysaccharide treatment significantly increased intracellular reactive oxygen species (ROS) levels and the early apoptotic rate in oocytes. The pro-apoptotic caspase-3 and Bax mRNA levels and caspase-3 protein level were significantly increased, whereas the anti-apoptotic Bcl-2 and XIAP transcript abundance were significantly decreased in lipopolysaccharide exposure group. Furthermore, the dimethyl-histone H3 lysine 4 (H3K4me2) level was significantly increased, while the DNA methylation (5-mC) and dimethyl-histone H3 lysine 9 (H3K9me2) levels were markedly decreased in oocytes treated with lipopolysaccharide. In conclusion, lipopolysaccharide exposure inhibits the maturation potential of bovine oocytes by affecting cell cycle, cytoskeletal dynamics, oxidative stress, and epigenetic modifications.
All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.