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衰老过程中线粒体缺陷在小鼠和人类中积累的差异。

Differences in the accumulation of mitochondrial defects with age in mice and humans.

机构信息

Mitochondrial Research Group, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.

出版信息

Mech Ageing Dev. 2011 Nov-Dec;132(11-12):588-91. doi: 10.1016/j.mad.2011.10.004. Epub 2011 Oct 12.

Abstract

Mitochondrial DNA mutations and associated defects in cytochrome c oxidase (COX) are proposed to play an important role in human ageing; however there have been limited studies on the frequency of these defects in normal mouse ageing. Here we compare COX-deficiency in two epithelial tissues; the colon and the ciliary epithelium, from human and mouse. The pattern of accumulation of COX-deficiency is similar in both tissues in the two species; however the frequency of colonic crypts with COX-deficiency in aged humans is significantly higher than in aged mice, whereas the levels of COX-deficiency in the ciliary epithelium are higher in the mouse than in humans. This suggests the impact of mitochondrial defects on normal ageing may differ significantly between species.

摘要

线粒体 DNA 突变和细胞色素 c 氧化酶 (COX) 相关缺陷被认为在人类衰老中起重要作用;然而,关于这些缺陷在正常小鼠衰老中的发生频率的研究有限。在这里,我们比较了两种上皮组织(结肠和睫状上皮)中 COX 缺陷在人和小鼠中的差异。两种组织中 COX 缺陷的积累模式在两种物种中相似;然而,在老年人中,结肠隐窝 COX 缺陷的频率在人类中明显高于在小鼠中,而睫状上皮中的 COX 缺陷水平在小鼠中高于人类。这表明线粒体缺陷对正常衰老的影响在不同物种之间可能有很大差异。

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