American Center for Reproductive Medicine, Department of Urology, Cleveland Clinic Foundation, Cleveland, Ohio; Redox Biology Laboratory, Department of Zoology, School of Life Sciences, Ravenshaw University, Odisha, India.
American Center for Reproductive Medicine, Department of Urology, Cleveland Clinic Foundation, Cleveland, Ohio.
J Urol. 2018 Aug;200(2):414-422. doi: 10.1016/j.juro.2018.03.009. Epub 2018 Mar 9.
Varicocele may disrupt testicular microcirculation and induce hypoxia-ischemia related degenerative changes in testicular cells and spermatozoa. Superoxide production at low oxygen concentration exacerbates oxidative stress in men with varicocele. Therefore, the current study was designed to study the role of mitochondrial redox regulation and its possible involvement in sperm dysfunction in varicocele associated infertility.
We identified differentially expressed mitochondrial proteins in 50 infertile men with varicocele and in 10 fertile controls by secondary liquid chromatography-tandem mass spectroscopy data driven in silico analysis. Identified proteins were validated by Western blot and immunofluorescence. Seminal oxidation-reduction potential was measured.
We identified 22 differentially expressed proteins related to mitochondrial structure (LETM1, EFHC, MIC60, PGAM5, ISOC2 and import TOM22) and function (NDFSU1, UQCRC2 and COX5B, and the core enzymes of carbohydrate and lipid metabolism). Cluster analysis and 3-dimensional principal component analysis revealed a significant difference between the groups. All proteins studied were under expressed in infertile men with varicocele. Liquid chromatography-tandem mass spectroscopy data were corroborated by Western blot and immunofluorescence. Impaired mitochondrial function was associated with decreased expression of the proteins (ATPase1A4, HSPA2, SPA17 and APOA1) responsible for proper sperm function, concomitant with elevated seminal oxidation-reduction potential in the semen of infertile patients with varicocele.
Impaired mitochondrial structure and function in varicocele may lead to oxidative stress, reduced ATP synthesis and sperm dysfunction. Mitochondrial differentially expressed proteins should be explored for the development of biomarkers as a predictor of infertility in patients with varicocele. Antioxidant therapy targeting sperm mitochondria may help improve the fertility status of these patients.
精索静脉曲张可能会破坏睾丸微循环,并导致睾丸细胞和精子发生与缺氧缺血相关的退行性变化。在低氧浓度下,超氧化物的产生会加剧精索静脉曲张患者的氧化应激。因此,本研究旨在研究线粒体氧化还原调节的作用及其在精索静脉曲张相关不育症中精子功能障碍中的可能作用。
我们通过二次液相色谱-串联质谱数据驱动的计算机分析,鉴定了 50 名精索静脉曲张不育男性和 10 名生育能力正常男性的差异表达线粒体蛋白。通过 Western blot 和免疫荧光验证鉴定出的蛋白。测量精液氧化还原电位。
我们鉴定出与线粒体结构(LETM1、EFHC、MIC60、PGAM5、ISOC2 和导入 TOM22)和功能(NDFSU1、UQCRC2 和 COX5B,以及碳水化合物和脂质代谢的核心酶)相关的 22 种差异表达蛋白。聚类分析和三维主成分分析显示两组之间存在显著差异。所有研究的蛋白在精索静脉曲张不育男性中表达均下调。液相色谱-串联质谱数据得到 Western blot 和免疫荧光的验证。线粒体功能受损与负责精子正常功能的蛋白(ATPase1A4、HSPA2、SPA17 和 APOA1)表达下调有关,同时精索静脉曲张不育患者精液中的氧化还原电位升高。
精索静脉曲张中线粒体结构和功能受损可能导致氧化应激、ATP 合成减少和精子功能障碍。线粒体差异表达蛋白可作为预测精索静脉曲张患者不育的生物标志物进行探索。针对精子线粒体的抗氧化治疗可能有助于改善这些患者的生育状况。