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Impact of precise modulation of reactive oxygen species levels on spermatozoa proteins in infertile men

机译:精确调节活性氧水平对不育男性精子蛋白的影响

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Background: Elevated levels of reactive oxygen species (ROS) are detected in 25% to 80% of infertile men. They are involved in the pathology of male infertility. Understanding the effect of increasing levels of ROS on the differential expression of sperm proteins is important to understand the cellular processes and or/pathways that may be implicated in male infertility. The aim of this study was to examine differentially expressed proteins (DEPs) in spermatozoa from patients with low, medium and high ROS levels.Methods: A total of 42 infertile men presenting for infertility and 17 proven fertile men were enrolled in the study. ROS levels were measured by chemiluminescence assay. Infertile men were divided into Low (0- < 93 RLU/s/106 sperm) (n = 11), Medium (>93-500 RLU/s/106 sperm) (n = 17) and High ROS (>500 RLU/s/106 sperm) group (n = 14). All fertile men had ROS levels between 4-50 RLU/s/106 sperm. 4 subjects from fertile group and 4 each from the Low, Medium and High ROS were pooled. Protein extraction, protein estimation, gel separation of the proteins, in-gel digestion, LTQ-orbitrap elite hybrid mass spectrometry system was conducted. The DEPs, the cellular localization and pathways of DEPs involved were examined utilizing bioinformatics tools.Results: 1035 proteins were identified in the 3 groups by global proteomic analysis. Of these, 305 were DEPs. 51 were unique to the Low ROS group, 47 Medium ROS group and 104 were unique to the High ROS group. 6 DEPs were identified by Uniprot and DAVID that had distinct reproductive functions and they were expressed only in 3 ROS groups but not in the control.Conclusions: We have for the first time demonstrated the presence of 6 DEPs with distinct reproductive functions only in men with low, medium or high ROS levels. These DEPs can serve as potential biomarkers of oxidative stress induced male infertility.
机译:背景:在25%至80%的不育男性中检测到活性氧(ROS)水平升高。他们参与了男性不育的病理。了解ROS水平升高对精子蛋白质差异表达的影响对于理解可能与男性不育症有关的细胞过程和/或途径很重要。这项研究的目的是检查ROS水平低,中和高的患者精子中的差异表达蛋白(DEPs)。方法:共有42名具有不育症的不育男性和17名经证实的具有生育能力的男性参与研究。通过化学发光测定法测量ROS水平。不育男性分为低(0- <93 RLU / s / 106精子)(n = 11),中(> 93-500 RLU / s / 106精子)(n = 17)和高ROS(> 500 RLU / s / 106精子)组(n = 14)。所有可育男性的ROS水平在4-50 RLU / s / 106精子之间。汇集了来自可育组的4名受试者和来自低,中和高ROS的4名受试者。进行了蛋白质提取,蛋白质估计,蛋白质的凝胶分离,凝胶内消化,LTQ-orbitrap精英混合质谱系统。使用生物信息学工具检测了DEPs,DEPs的细胞定位和途径。结果:通过全局蛋白质组学分析,在3组中鉴定出1035种蛋白质。其中,有305个是DEP。低ROS组独特的有51个,中ROS组独特的有47个,高ROS组独特的有104个。 Uniprot和DAVID鉴定出6种具有不同生殖功能的DEPs,它们仅在3个ROS组中表达,而在对照组中没有表达。结论:我们首次证明只有在男性中存在6种具有不同生殖功能的DEPs。 ROS水平低,中或高。这些DEP可以作为氧化应激诱导的男性不育的潜在生物标志物。

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