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Age-dependent changes in mitochondrial morphology and volume are not predictors of lifespan

机译:线粒体形态和体积的年龄依赖性变化不是寿命的预测因子

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摘要

Mitochondrial dysfunction is a hallmark of skeletal muscle degeneration during aging. One mechanism through which mitochondrial dysfunction can be caused is through changes in mitochondrial morphology. To determine the role of mitochondrial morphology changes in age-dependent mitochondrial dysfunction, we studied mitochondrial morphology in body wall muscles of the nematode C. elegans. We found that in this tissue, animals display a tubular mitochondrial network, which fragments with increasing age. This fragmentation is accompanied by a decrease in mitochondrial volume. Mitochondrial fragmentation and volume loss occur faster under conditions that shorten lifespan and occur slower under conditions that increase lifespan. However, neither mitochondrial morphology nor mitochondrial volume of five- and seven-day old wild-type animals can be used to predict individual lifespan. Our results indicate that while mitochondria in body wall muscles undergo age-dependent fragmentation and a loss in volume, these changes are not the cause of aging but rather a consequence of the aging process.
机译:线粒体功能障碍是衰老过程中骨骼肌变性的标志。可以引起线粒体功能障碍的一种机制是通过改变线粒体的形态。为了确定线粒体形态变化在年龄依赖性线粒体功能障碍中的作用,我们研究了线虫秀丽隐杆线虫体壁肌肉中的线粒体形态。我们发现,在这种组织中,动物显示出管状的线粒体网络,该网络随着年龄的增长而破碎。这种分裂伴随着线粒体体积的减少。线粒体破碎和体积损失在缩短寿命的条件下发生较快,而在增加寿命的条件下发生较慢。但是,五日龄和七日龄野生型动物的线粒体形态和线粒体体积均不能用于预测个体寿命。我们的结果表明,尽管体壁肌肉中的线粒体经历了年龄依赖性的破碎和体积损失,但这些变化并不是衰老的原因,而是衰老过程的结果。

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