Key Laboratory of Freshwater Aquatic Resources, Ministry of Agriculture and Rural Affairs, Shanghai Ocean University, Shanghai 201306, PR China.
International Research Center for Marine Biosciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
J Proteome Res. 2021 May 7;20(5):2923-2934. doi: 10.1021/acs.jproteome.1c00144. Epub 2021 Apr 14.
Hypoxia is one of the major stresses in aquaculture animals. Recently, we reported that hypoxia disrupts the endocrine system and inhibits testicular function of oriental river prawns (), but the molecular mechanism of testes responded to hypoxia remains largely unknown. In the present study, we aimed to integrate whole phosphoproteomic profiles of hypoxia-treated testes of the oriental river prawn (). We successfully isolated sperm cells and evaluated the mitochondrial morphology and function using laser confocal microscopy, flow cytometry, and biochemical analyses. Quantitative proteomics identified 117 differentially abundant phosphorylated proteins, and these proteins are mainly involved in the pathways related to cellular processes, including autophagy, apoptosis, and the FoxO signaling pathway. Protein-protein interaction analysis clustered these phosphoproteins into three groups, many of which have been suggested to impact carbohydrate metabolism, autophagy, and signal regulation in testes. Western blotting confirmed that phosphorylated proteins including AMPK, ULK1, and TP53 (of the AMPK pathway) may contribute to testicular dysfunction caused by hypoxia. Further, we investigated the potential roles of AMP-activated protein kinase (AMPK)'s in testes mitochondrial autophagy and apoptosis in as induced by hypoxia. Simultaneous knockdown of AMPKα in sperm cells led to a decrease in FOXO3a phosphorylation at Ser413, upregulation of caspase-3 and caspase-9 activities, and an increased apoptosis rate. These results improve our understanding of hypoxia-induced energy metabolism disorders in the testes of .
缺氧是水产养殖动物面临的主要应激之一。最近,我们报道了缺氧会破坏东方沼虾()的内分泌系统并抑制其睾丸功能,但睾丸对缺氧的反应的分子机制在很大程度上仍然未知。在本研究中,我们旨在整合缺氧处理的东方沼虾睾丸的全磷酸化蛋白质组图谱()。我们成功分离了精子细胞,并使用激光共聚焦显微镜、流式细胞术和生化分析评估了线粒体形态和功能。定量蛋白质组学鉴定出 117 个差异丰度磷酸化蛋白,这些蛋白主要参与与细胞过程相关的途径,包括自噬、细胞凋亡和 FoxO 信号通路。蛋白质-蛋白质相互作用分析将这些磷酸化蛋白聚类为三组,其中许多已被建议影响睾丸中的碳水化合物代谢、自噬和信号调节。Western blot 验证了磷酸化蛋白,包括 AMPK、ULK1 和 TP53(AMPK 途径),可能导致缺氧引起的睾丸功能障碍。此外,我们研究了缺氧诱导的 AMPK 在东方沼虾精子细胞中线粒体自噬和细胞凋亡中的作用。AMPKα 在精子细胞中的同时敲低导致 FOXO3a 在 Ser413 处的磷酸化减少、caspase-3 和 caspase-9 活性上调以及凋亡率增加。这些结果提高了我们对缺氧引起的东方沼虾睾丸能量代谢紊乱的理解。