Mitochondrial Dysfunction Accelerates Ageing.

Johannes Schroth, Sian M Henson
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引用次数: 3

Abstract

We review here the seminal findings of Desdin-Mico et al. showing that T cells with dysfunctional mitochondria induce multimorbity and premature senescence, due to mitochondrial transcription factor A (TFAM). They add further weight to the idea that targeting immunometabolism could be beneficial in combating the detrimental effects of age-related disease.

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线粒体功能障碍加速衰老。
我们在此回顾Desdin-Mico等人的开创性发现,这些发现表明线粒体功能障碍的T细胞由于线粒体转录因子A (TFAM)而诱导多病变和过早衰老。他们进一步支持了这样一种观点,即以免疫代谢为目标可能有助于对抗与年龄有关的疾病的有害影响。
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