Mitochondrial function in peripheral blood cells across the human lifespan.

IF 4.1 Q2 GERIATRICS & GERONTOLOGY npj aging Pub Date : 2024-02-07 DOI:10.1038/s41514-023-00130-4
Johannes K Ehinger, Emil Westerlund, Eleonor Åsander Frostner, Michael Karlsson, Gesine Paul, Fredrik Sjövall, Eskil Elmér
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Abstract

Mitochondrial dysfunction is considered a hallmark of aging. Up to now, a gradual decline of mitochondrial respiration with advancing age has mainly been demonstrated in human muscle tissue. A handful of studies have examined age-related mitochondrial dysfunction in human blood cells, and only with small sample sizes and mainly in platelets. In this study, we analyzed mitochondrial respiration in peripheral blood mononuclear cells (PBMCs) and platelets from 308 individuals across the human lifespan (0-86 years). In regression analyses, with adjustment for false discovery rate (FDR), we found age-related changes in respiratory measurements to be either small or absent. The main significant changes were an age-related relative decline in complex I-linked respiration and a corresponding rise of complex II-linked respiration in PBMCs. These results add to the understanding of mitochondrial dysfunction in aging and to its possible role in immune cell and platelet senescence.

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人一生中外周血细胞的线粒体功能。
线粒体功能障碍被认为是衰老的标志。迄今为止,线粒体呼吸随年龄增长而逐渐下降的现象主要在人体肌肉组织中得到证实。只有少数研究检测了人血细胞中与年龄相关的线粒体功能障碍,而且样本量很小,主要是在血小板中。在这项研究中,我们分析了来自 308 人的外周血单核细胞(PBMCs)和血小板的线粒体呼吸,这些细胞来自人的整个生命周期(0-86 岁)。在对误诊率(FDR)进行调整的回归分析中,我们发现呼吸测量值与年龄相关的变化要么很小,要么没有。主要的重大变化是,与年龄相关的复合 I 链呼吸相对下降,而与年龄相关的复合 II 链呼吸相应上升。这些结果加深了人们对衰老过程中线粒体功能障碍及其在免疫细胞和血小板衰老过程中可能扮演的角色的认识。
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