线粒体和端粒:携手合作。

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY
Biogerontology Pub Date : 2024-04-01 Epub Date: 2023-10-21 DOI:10.1007/s10522-023-10074-7
Mélina Vaurs, Elif Beyza Dolu, Anabelle Decottignies
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引用次数: 0

摘要

作为一种内共生体,14.5亿年前被原真核细胞吞噬的细菌逐渐进化为一种重要的细胞器,与宿主细胞有多种相互作用。特别是,线粒体和染色体末端端粒之间的紧密联系,提出了一种新的衰老理论,其中功能失调的端粒和线粒体是降低细胞健康度和促进细胞衰老的恶性循环的主要参与者。我们综述了氧化应激和线粒体功能障碍损害端粒的证据,并通过穿梭于细胞核和线粒体之间的端粒酶的透镜进一步讨论了端粒生物学与线粒体之间的相互关系。最后,我们详细阐述了线粒体基因组通过线粒体基因变体的表达在人类端粒长度遗传中的可能作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mitochondria and telomeres: hand in glove.

Mitochondria and telomeres: hand in glove.

Born as an endosymbiont, the bacteria engulfed by the proto-eukaryotic cell more than 1.45 billion years ago progressively evolved as an important organelle with multiple interactions with the host cell. In particular, strong connections between mitochondria and the chromosome ends, the telomeres, led to propose a new theory of ageing in which dysfunctional telomeres and mitochondria are the main actors of a vicious circle reducing cell fitness and promoting cellular ageing. We review the evidences that oxidative stress and dysfunctional mitochondria damage telomeres and further discuss the interrelationship between telomere biology and mitochondria through the lens of telomerase which shuttles between the nucleus and mitochondria. Finally, we elaborate on the possible role of the mitochondrial genome on the inheritance of human telomere length through the expression of mitochondrial gene variants.

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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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