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Exercise reduces circulating biomarkers of cellular senescence in humans

机译:运动减少人类细胞衰老的循环生物标志物

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摘要

Cellular senescence has emerged as a significant and potentially tractable mechanism of aging and multiple aging‐related conditions. Biomarkers of senescent cell burden, including molecular signals in circulating immune cells and the abundance of circulating senescence‐related proteins, have been associated with chronological age and clinical parameters of biological age in humans. The extent to which senescence biomarkers are affected by interventions that enhance health and function has not yet been examined. Here, we report that a 12‐week structured exercise program drives significant improvements in several performance‐based and self‐reported measures of physical function in older adults. Impressively, the expression of key markers of the senescence program, including p16, p21, cGAS, and TNFα, were significantly lowered in CD3+ T cells in response to the intervention, as were the circulating concentrations of multiple senescence‐related proteins. Moreover, partial least squares discriminant analysis showed levels of senescence‐related proteins at baseline were predictive of changes in physical function in response to the exercise intervention. Our study provides first‐in‐human evidence that biomarkers of senescent cell burden are significantly lowered by a structured exercise program and predictive of the adaptive response to exercise.
机译:细胞衰老已经成为老龄化和老龄化的多个相关条件的显著和潜在的易处理机制。的衰老细胞的负担,其中包括在循环免疫细胞的分子信号和循环衰老相关的蛋白质的丰度,生物标志物已与实足年龄和人类生物学年龄的临床参数。到衰老的生物标志物是由增强健康和功能的干预措施的影响程度尚未审查。在这里,我们报告说,在中老年人身体机能的几个基于表现,自我报告的措施,12周的结构化的锻炼计划驱动显著的改善。令人印象深刻,衰老方案的主要标记,包括p16蛋白的表达, P21,CGAS,和TNFα,在CD3 + T细胞显著降低响应于干预,因为是多个衰老相关蛋白的循环浓度。在基线衰老相关的蛋白质。此外,偏最小二乘法判别分析显示水平响应运动干预是预测身体机能的变化。我们的研究提供了首次在人类的证据表明,衰老细胞负担生物标志物显著通过结构化的锻炼计划降低和预测锻炼的适应性反应。

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