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线粒体蛋白酶:线粒体可塑性的多面调节因子。

Mitochondrial Proteases: Multifaceted Regulators of Mitochondrial Plasticity.

机构信息

Max Planck Institute for Biology of Ageing, 50931 Cologne, Germany; email:

Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.

出版信息

Annu Rev Biochem. 2020 Jun 20;89:501-528. doi: 10.1146/annurev-biochem-062917-012739. Epub 2020 Feb 19.

Abstract

Mitochondria are essential metabolic hubs that dynamically adapt to physiological demands. More than 40 proteases residing in different compartments of mitochondria, termed mitoproteases, preserve mitochondrial proteostasis and are emerging as central regulators of mitochondrial plasticity. These multifaceted enzymes limit the accumulation of short-lived, regulatory proteins within mitochondria, modulate the activity of mitochondrial proteins by protein processing, and mediate the degradation of damaged proteins. Various signaling cascades coordinate the activity of mitoproteases to preserve mitochondrial homeostasis and ensure cell survival. Loss of mitoproteases severely impairs the functional integrity of mitochondria, is associated with aging, and causes pleiotropic diseases. Understanding the dual function of mitoproteases as regulatory and quality control enzymes will help unravel the role of mitochondrial plasticity in aging and disease.

摘要

线粒体是重要的代谢中心,能够动态适应生理需求。超过 40 种位于线粒体不同隔室的蛋白酶被称为线粒体蛋白酶,它们维持着线粒体的蛋白质稳态,并成为线粒体可塑性的核心调节因子。这些多方面的酶限制了寿命短的调节蛋白在线粒体中的积累,通过蛋白质加工调节线粒体蛋白的活性,并介导受损蛋白的降解。各种信号级联反应协调线粒体蛋白酶的活性,以维持线粒体的动态平衡并确保细胞的存活。线粒体蛋白酶的缺失严重损害了线粒体的功能完整性,与衰老有关,并导致多种疾病。了解线粒体蛋白酶作为调节和质量控制酶的双重功能将有助于揭示线粒体可塑性在衰老和疾病中的作用。

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