人类衰老过程中骨骼肌mtDNA的定性和定量变化及线粒体编码基因的表达

Antoni Barrientos , Jordi Casademont , Francesc Cardellach , Esther Ardite , Xavier Estivill , Alvaro Urbano-Márquez , J.Carlos Fernández-Checa , Virginia Nunes
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引用次数: 89

摘要

人们普遍认为,线粒体遗传系统的年龄依赖性变化可能有助于人类衰老过程。我们最近报道了线粒体呼吸链酶的特定活性不变,不同底物的氧化能力随着年龄的增长而下降,部分原因是一些混杂变量,如体育活动或烟草消费。目前的研究涉及与年龄相关的肌肉mtDNA结构的变化及其在人类的生物发生。我们发现mtDNA重排随年龄增长的发生率较低,仅通过PCR检测到。mtDNA含量随年龄的增长而显著增加(b= 0.0115,P<0.0001)。此外,线粒体转录物的稳态水平不变,转录率降低(P<0.0001),线粒体膜脂过氧化增加(P<0.0001)。这些数据表明,在人类衰老过程中出现了微小的mtDNA结构变化。相比之下,线粒体稳态的改变最终导致线粒体生物发生速率的改变,可能在人类衰老过程中发挥作用。
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Qualitative and Quantitative Changes in Skeletal Muscle mtDNA and Expression of Mitochondrial-Encoded Genes in the Human Aging Process

It has been widely postulated that age-dependent changes in the mitochondrial genetic system may contribute to the human aging process. We recently reported unchanged specific activities of mitochondrial respiratory chain enzymes and a decrease in oxidation capacity of different substrates with aging, due, in part, to some confounding variables such as physical activity or tobacco consumption. The present study deals with age-related changes in muscle mtDNA structure and its biogenesis in humans. We found a low prevalence of mtDNA rearrangements with aging, only detected by PCR. The mtDNA content increased significantly with age (b= 0.0115,P< 0.0001). Also, an unchanged steady-state level of mitochondrial transcripts, a reduced transcription rate (P< 0.0001), and an increase in mitochondrial membrane lipid peroxidation (P< 0.0001) were observed in aging. These data demonstrate that minor structural mtDNA changes appear during the human aging process. By contrast, alterations in mitochondrial homeostasis ultimately producing modifications in mitochondrial biogenesis rates could play a role in the process of human senescence.

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