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线粒体蛋白质组的比较分析揭示了体外液体保存后碳离子辐射诱导公羊精子活力增强的机制。

Comparative Analysis of Mitochondrial Proteome Reveals the Mechanism of Enhanced Ram Sperm Motility Induced by Carbon Ion Radiation After In Vitro Liquid Storage.

作者信息

He Yuxuan, Li Hongyan, Zhang Yong, Hu Junjie, Shen Yulong, Feng Jin, Zhao Xingxu

机构信息

College of Veterinary Medicine, Gansu Agricultural University, Lanzhou, China.

Department of Radiation Medicine, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, China.

出版信息

Dose Response. 2019 Jan 10;17(1):1559325818823998. doi: 10.1177/1559325818823998. eCollection 2019 Jan-Mar.

Abstract

The aim of this study was to reveal the mechanism of enhanced ram sperm motility induced by heavy ion radiation (HIR) after in vitro liquid storage. Ram semen was stored for 24 hours at 5°C and then irradiated with 0.1 Gy carbon ion radiation (CIR). In comparison to nonirradiated (NIR) sperm, the motility, viability, and adenosine triphosphate content were all higher in CIR sperm, and the reactive oxygen species levels were lower. Moreover, 87 differential mitochondrial protein spots were detected in 2-dimensional gels between CIR and NIR sperm and were identified as 52 corresponding proteins. In addition, 33 differential proteins were involved in a main pathway network, including COX5B, ERAB/HSD17B10, ETFA, SDHB, and SOD2, which are known to be involved in cell communication, energy production, and antioxidant responses. We used immunoblotting and immunofluorescence to analyze the content and localization of these proteins, respectively, and the levels of these proteins in CIR sperm were lower than those in NIR sperm. An understanding of the molecular function of these proteins could provide further insight into the mechanisms underlying high sperm motility induced by HIR in rams.

摘要

本研究的目的是揭示体外液体保存后重离子辐射(HIR)诱导公羊精子活力增强的机制。公羊精液在5°C下保存24小时,然后用0.1 Gy碳离子辐射(CIR)照射。与未照射(NIR)的精子相比,CIR精子的活力、存活率和三磷酸腺苷含量均更高,活性氧水平更低。此外,在二维凝胶中检测到CIR和NIR精子之间有87个差异线粒体蛋白斑点,并鉴定出52个相应的蛋白质。另外,33种差异蛋白参与了一个主要的通路网络,包括COX5B、ERAB/HSD17B10、ETFA、SDHB和SOD2,已知这些蛋白参与细胞通讯、能量产生和抗氧化反应。我们分别使用免疫印迹和免疫荧光分析这些蛋白的含量和定位,CIR精子中这些蛋白的水平低于NIR精子。了解这些蛋白的分子功能可以进一步深入了解HIR诱导公羊精子高活力的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/139d/6343446/5cc43b43c472/10.1177_1559325818823998-fig1.jpg

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