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靶向线粒体-蛋白质稳态轴以延缓衰老。

Targeting the Mitochondria-Proteostasis Axis to Delay Aging.

作者信息

Zimmermann Andreas, Madreiter-Sokolowski Corina, Stryeck Sarah, Abdellatif Mahmoud

机构信息

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Field of Excellence BioHealth - University of Graz, Graz, Austria.

出版信息

Front Cell Dev Biol. 2021 Mar 11;9:656201. doi: 10.3389/fcell.2021.656201. eCollection 2021.

Abstract

Human life expectancy continues to grow globally, and so does the prevalence of age-related chronic diseases, causing a huge medical and economic burden on society. Effective therapeutic options for these disorders are scarce, and even if available, are typically limited to a single comorbidity in a multifaceted dysfunction that inevitably affects all organ systems. Thus, novel therapies that target fundamental processes of aging itself are desperately needed. In this article, we summarize current strategies that successfully delay aging and related diseases by targeting mitochondria and protein homeostasis. In particular, we focus on autophagy, as a fundamental proteostatic process that is intimately linked to mitochondrial quality control. We present genetic and pharmacological interventions that effectively extend health- and life-span by acting on specific mitochondrial and pro-autophagic molecular targets. In the end, we delve into the crosstalk between autophagy and mitochondria, in what we refer to as the mitochondria-proteostasis axis, and explore the prospect of targeting this crosstalk to harness maximal therapeutic potential of anti-aging interventions.

摘要

全球人类预期寿命持续增长,与年龄相关的慢性病患病率也在上升,给社会带来了巨大的医疗和经济负担。针对这些疾病的有效治疗方法稀缺,即便有,通常也仅限于多方面功能障碍中的单一合并症,而这种功能障碍不可避免地会影响所有器官系统。因此,迫切需要针对衰老基本过程的新型疗法。在本文中,我们总结了目前通过靶向线粒体和蛋白质稳态来成功延缓衰老及相关疾病的策略。特别地,我们聚焦于自噬,它作为一种基本的蛋白质稳态过程,与线粒体质量控制密切相关。我们介绍了通过作用于特定线粒体和促自噬分子靶点来有效延长健康寿命和寿命的基因和药物干预措施。最后,我们深入探讨自噬与线粒体之间的相互作用,即我们所说的线粒体 - 蛋白质稳态轴,并探索靶向这种相互作用以发挥抗衰老干预最大治疗潜力的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaf0/7991595/f976e310cc8d/fcell-09-656201-g001.jpg

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