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溶酶体膜通透性改变与细胞死亡。

Lysosomal membrane permeabilization and cell death.

机构信息

Unit Biotechnology and Cell Signaling/Laboratory of Excellence Medalis, CNRS/Université de Strasbourg, Illkirch, France.

Departament of Cellular and Molecular Biology, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.

出版信息

Traffic. 2018 Dec;19(12):918-931. doi: 10.1111/tra.12613. Epub 2018 Sep 12.

Abstract

Lysosomes are membrane-enclosed organelles that mediate the intracellular degradation of macromolecules. They play an essential role in calcium regulation and have emerged as key signaling hubs in controlling the nutrient response. Maintaining lysosomal integrity and function is therefore crucial for cellular homeostasis. Different forms of stress can induce lysosomal membrane permeabilization (LMP), resulting in the translocation to the cytoplasm of intralysosomal components, such as cathepsins, inducing lysosomal-dependent cell death (LDCD). Here, we review recent advances that have furthered our understanding of the molecular mechanisms of LMP and the methods used to detect it. We discuss several endolysosomal damage-response mechanisms that mediate the repair or elimination of compromised lysosomes and summarize the role of LMP and cathepsins in LDCD and other cell death pathways. Finally, with the emergence of lysosomes as promising therapeutic targets for several human diseases, we review a variety of therapeutic strategies that seek to either destabilize lysosomes or to maintain, enhance or restore lysosomal function.

摘要

溶酶体是一种膜结合的细胞器,介导细胞内大分子的降解。它们在钙调节中起着重要作用,并且已经成为控制营养响应的关键信号枢纽。因此,维持溶酶体的完整性和功能对于细胞内稳态至关重要。不同形式的应激可以诱导溶酶体膜通透性(LMP),导致溶酶体内成分(如组织蛋白酶)向细胞质易位,诱导溶酶体依赖性细胞死亡(LDCD)。在这里,我们回顾了最近的进展,这些进展进一步加深了我们对 LMP 的分子机制以及检测方法的理解。我们讨论了几种内溶酶体损伤反应机制,这些机制介导受损溶酶体的修复或消除,并总结了 LMP 和组织蛋白酶在 LDCD 和其他细胞死亡途径中的作用。最后,随着溶酶体作为几种人类疾病有前途的治疗靶点的出现,我们回顾了各种旨在破坏溶酶体或维持、增强或恢复溶酶体功能的治疗策略。

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