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Muscle Proteomic and Transcriptomic Profiling of Healthy Aging and Metabolic Syndrome in Men

机译:男性健康衰老和代谢综合征的肌肉蛋白质组学和转录组分析

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(1) Background: Aging is associated with a progressive decline in muscle mass and function. Aging is also a primary risk factor for metabolic syndrome, which further alters muscle metabolism. However, the molecular mechanisms involved remain to be clarified. Herein we performed omic profiling to decipher in muscle which dominating processes are associated with healthy aging and metabolic syndrome in old men. (2) Methods: This study included 15 healthy young, 15 healthy old, and 9 old men with metabolic syndrome. Old men were selected from a well-characterized cohort, and each vastus lateralis biopsy was used to combine global transcriptomic and proteomic analyses. (3) Results: Over-representation analysis of differentially expressed genes (ORA) and functional class scoring of pathways (FCS) indicated that healthy aging was mainly associated with upregulations of apoptosis and immune function and downregulations of glycolysis and protein catabolism. ORA and FCS indicated that with metabolic syndrome the dominating biological processes were upregulation of proteolysis and downregulation of oxidative phosphorylation. Proteomic profiling matched 586 muscle proteins between individuals. The proteome of healthy aging revealed modifications consistent with a fast-to-slow transition and downregulation of glycolysis. These transitions were reduced with metabolic syndrome, which was more associated with alterations in NADH/NAD+ shuttle and β-oxidation. Proteomic profiling further showed that all old muscles overexpressed protein chaperones to preserve proteostasis and myofiber integrity. There was also evidence of aging-related increases in reactive oxygen species but better detoxifications of cytotoxic aldehydes and membrane protection in healthy than in metabolic syndrome muscles. (4) Conclusions: Most candidate proteins and mRNAs identified herein constitute putative muscle biomarkers of healthy aging and metabolic syndrome in old men.
机译:(1)背景:衰老与肌肉质量和功能的进行性减退相关联。老化也是代谢综合症,其进一步涂改肌肉代谢的主要危险因素。然而,所涉及的分子机制仍有待阐明。在这里我们进行分析OMIC在肌肉解密其主导工艺与健康老龄化和老年男性代谢综合征相关。 (2)方法:这项研究包括15名健康的年轻,健康的15岁和9岁的男人与代谢综合征。从充分表征的群体选择老矣,每一股外侧肌活检用于全球转录组和蛋白质组分析结合起来。 (3)结果:差异表达的基因(ORA)和途径的功能类别的得分(FCS)过表达分析表明,健康老化,主要与细胞凋亡和免疫功能的upregulations和糖酵解和蛋白质分解代谢的downregulations相关联。 ORA和FCS表明,代谢综合征占主导地位的生物过程是蛋白质水解和氧化磷酸化的下调上调。蛋白质组图谱匹配的个体之间586个肌肉蛋白。健康老龄化的蛋白质组揭示了与糖酵解快到慢的转变和下调相一致的修改。这些过渡代谢综合征,这是更与NADH / NAD +班车和β氧化改变相关减少。蛋白质组图谱进一步表明,所有旧的肌肉过度表达的蛋白质分子伴侣保护蛋白内稳态和肌纤维的完整性。还有的活性氧与老化相关的增加,但细胞毒性醛和健康比在代谢综合征的肌肉膜保护的更好detoxifications证据。 (4)结论:认定大多数候选蛋白的mRNA,并在此构成健康老龄化与老年男性代谢综合征的假定肌肉的生物标志物。

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