Ying-Jie Niu, Dongjie Zhou, Wenjun Zhou, Zheng-Wen Nie, Ju-Yeon Kim, YoungJin Oh, So-Rim Lee, Xiang-Shun Cui
언어
영어(ENG)
URL
https://www.earticle.net/Article/A378895
※ 기관로그인 시 무료 이용이 가능합니다.
4,000원
원문정보
초록
영어
Nitric oxide (NO)-induced protein S-nitrosylation triggers mitochondrial dysfunction and was related to cell senescence. However, the exact mechanism of these damages is not clear. In the present study, to investigate the relationship between in vitro aging and NO-induced protein S-nitrosylation, oocytes were treated with sodium nitroprusside dihydrate (SNP), and the resultant S-nitrosylated proteins were detected through biotin-switch assay. The results showed that levels of protein S-nitroso thiols (SNO)s and expression of S-nitrosoglutathione reductase (GSNOR) increased, while activity and function of mitochondria were impaired during oocyte aging. Addition of SNP, a NO donor, to the oocyte culture led to accelerated oocyte aging, increased mitochondrial dysfunction and damage, apoptosis, ATP deficiency, and enhanced ROS production. These results suggested that the increased NO signal during oocyte aging in vitro, accelerated oocyte degradation due to increased protein S-nitrosylation, and ROS-related redox signaling.
목차
ABSTRACT INTRODUCTION MATERIALS AND METHODS Collection and in vitro maturation of cattle oocytes In vitro aging and SNP treatment Biotin-switchd assay for detection of S-nitrosylated proteins ROS measurements Total and active mitochondrial staining Immunofluorescence and confocal microscopy Analysis of MtDNA copy number ATP measurements Statistical analysis RESULTS Protein SNO level and GSNOR expression increases during oocyte aging Mitochondrial activity and function decrease during oocyte aging Treatment with SNP increases protein SNO level and leads to accumulation of damaged mitochondria Treatment with SNP increases ROS production and apoptosis level DISCUSSION CONFLICTS OF INTEREST ACKNOWLEDGEMENTS AUTHOR CONTRIBUTIONS AUTHOR’S POSITION AND ORCID NO. REFERENCES