首页> 外文期刊>Antioxidants and redox signalling >Aberrant Upregulation of Compensatory Redox Molecular Machines May Contribute to Sperm Dysfunction in Infertile Men with Unilateral Varicocele: A Proteomic Insight
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Aberrant Upregulation of Compensatory Redox Molecular Machines May Contribute to Sperm Dysfunction in Infertile Men with Unilateral Varicocele: A Proteomic Insight

机译:代偿性氧化还原的异常上调可能有助于单侧毒素的不育男性的精子功能障碍:蛋白质组学洞察力

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Aims: To understand the molecular pathways involved in oxidative stress (OS)-mediated sperm dysfunction against a hypoxic and hyperthermic microenvironment backdrop of varicocele through a proteomic approach.Results: Protein selection (261) based on their role in redox homeostasis and/or oxidative/hyperthermic/hypoxic stress response from the sperm proteome data set of unilateral varicocele (UV) in comparison with fertile control displayed 85 to be differentially expressed. Upregulation of cellular oxidant detoxification and glutathione and reduced nicotinamide adenine dinucleotide (NADH) metabolism accompanied with downregulation of protein folding, energy metabolism, and heat stress responses were observed in the UV group. Ingenuity pathway analysis (IPA) predicted suppression of oxidative phosphorylation (OXPHOS) (validated by Western blotting [WB]) along with augmentation in OS and mitochondrial dysfunction in UV. The top affected networks indicated by IPA involved heat shock proteins (HSPs: HSPA2 and HSP90B1). Their expression profile was corroborated by immunocytochemistry and WB. Hypoxia-inducible factor 1A as an upstream regulator of HSPs was predicted by MetaCore. Occurrence of reductive stress in UV spermatozoa was corroborated by thiol redox status.Innovation: This is the first evidence of a novel pathway showing aberrant redox homeostasis against chronic hypoxic insult in varicocele leading to sperm dysfunction.Conclusions: Upregulation of antioxidant system and dysfunctional OXPHOS would have shifted the redox balance of biological redox couples (GSH/GSSG, NAD+/NADH, and NADP+/NADPH) to a more reducing state leading to reductive stress. Chronic reductive stress-induced OS may be involved in sperm dysfunction in infertile men with UV, where the role of HSPs cannot be ignored. Intervention with antioxidant therapy warrants proper prior investigation.
机译:目的:要通过蛋白质组学方法了解氧化应激(OS)介导的氧化应激(OS)介导的精子功能障碍的分子途径。结果:蛋白质选择(261),基于它们在氧化还原稳态和/或氧化中的作用/从精子蛋白质组数据集的单侧VariCele(UV)的热热/缺氧应力响应与育种控制显示85进行差异表达。在UV基团中观察到伴随蛋白质折叠,能量代谢和热应激反应的细胞氧化剂排毒和谷胱甘肽腺嘌呤二核苷酸(NADH)代谢的上调,并在UV基团中观察到。 Indenuey途径分析(IPA)预测抑制氧化磷酸化(毒剂)(通过Western Blotting [Wb]验证)以及UV中的OS和线粒体功能障碍的增强。 IPA指示的顶层受影响的网络涉及热休克蛋白(HSPS:HSPA2和HSP90B1)。他们的表情谱通过免疫细胞化学和WB来证实。缺氧诱导因子1A作为HSP的上游调节剂被甲状腺手术预测。通过硫醇氧化铈状态证实了UV精子的还原胁迫的发生。这是一种新的途径的第一个证据,呈现出异常氧化还原性血管障碍的毒素,导致精子功能障碍。结论:抗氧化系统和功能障碍毒弹的上调已将生物氧化还原耦合(GSH / GSSG,NAD + / NADH和NADP + / NADH)的氧化还原平衡转移到更低的状态,导致还原应力。慢性还原应激诱导的OS可以参与具有UV的不育的人中的精子功能障碍,其中HSP的作用不能忽视。抗氧化治疗的干预认证认证。

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