炎症和代谢紊乱中单核细胞线粒体动力学特征

T. Tolstik, A. Bogatyreva, A. Grechko, Y. Oishi, A. Markin
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引用次数: 0

摘要

线粒体在细胞中不是单独存在的;它们形成了一个同质的网络,在这个网络中,分裂和融合的过程不断发生。这种平衡的改变,以及线粒体功能障碍,导致慢性和代谢疾病的发展。线粒体的代谢变化控制单核细胞的形成和分化。单核/巨噬细胞的促炎激活导致氧化磷酸化的减少和线粒体融合的增加。迄今为止,调节线粒体动力学以控制单核细胞生死的分子机制尚不清楚。此外,有充分证据表明线粒体代谢异常参与了许多疾病的发病机制。线粒体应激和损伤导致细胞死亡、代谢紊乱和炎症。在这篇综述中,我们详细考虑了线粒体过程在病理发展中的参与,并讨论了线粒体如何在治疗上受到影响。注意也提请到可能的诊断研究,目标线粒体动力学的疾病在单核细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of mitochondrial dynamics in monocytes in inflammatory and metabolic disorders
Mitochondria do not exist as separate formations in the cell; they form a homogeneous network in which the processes of division and fusion continuously occur. A shift in this balance, as well as mitochondrial dysfunction, leads to the development of chronic and metabolic disorders. Metabolic changes in mitochondria control the formation and differentiation of monocytes. Pro-inflammatory activation of monocytes/macrophages leads to a decrease in oxidative phosphorylation and an increase in mitochondrial fusion. To date, the molecular mechanisms that regulate mitochondrial dynamics to control life and death in monocytes are not well understood. In addition, there is ample evidence that abnormal mitochondrial metabolism is involved in the pathogenesis of many diseases. Mitochondrial stress and damage contribute to cell death, metabolic disorders, and inflammation. In this review, we consider in detail the involvement of mitochondrial processes in the development of pathologies and discuss how mitochondria can be therapeutically affected. Attention is also drawn to possible diagnostic studies that target mitochondrial dynamics of disorders in monocytes.
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CiteScore
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