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溶酶体损伤反应和溶酶体吞噬作用对受损溶酶体的检测和清除。

Detection and Clearance of Damaged Lysosomes by the Endo-Lysosomal Damage Response and Lysophagy.

机构信息

Molecular Biology I, Centre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, 45141 Essen, Germany.

出版信息

Curr Biol. 2017 Dec 18;27(24):R1330-R1341. doi: 10.1016/j.cub.2017.11.012.

Abstract

Lysosomal membrane permeabilization or lysosomal rupture is recognized as a common and severe stress condition relevant for infection, cellular degeneration and cancer. However, the cellular response mechanisms that protect cells from the consequences of lysosomal damage and ensure lysosomal quality control and homeostasis have only recently been explored. Key elements of this response involve the specific sensing of the damage followed by extensive modification of the organelles with ubiquitin to mark them for clearance by selective macroautophagy, termed lysophagy. Efficient lysophagy is ensured by additional layers of regulation, including modulation by the ubiquitin-directed AAA-ATPase VCP/p97. Lysophagy shares many features with mitophagy, the macroautophagic removal of damaged mitochondria. This review aims to gather available data from different fields and to define the key steps necessary for sensing and subsequent clearance of damaged lysosomes. We conclude with a discussion of disease implications with a focus on neurodegeneration.

摘要

溶酶体膜通透性或破裂被认为是一种常见且严重的应激状态,与感染、细胞变性和癌症有关。然而,最近才开始探索保护细胞免受溶酶体损伤后果并确保溶酶体质量控制和动态平衡的细胞反应机制。该反应的关键要素包括对损伤的特异性感应,随后通过泛素对细胞器进行广泛修饰,以标记它们通过选择性巨自噬(称为溶酶体自噬)进行清除。通过其他调节层来确保有效的溶酶体自噬,包括泛素导向的 AAA-ATPase VCP/p97 的调节。溶酶体自噬与线粒体自噬(即受损线粒体的巨自噬去除)有许多共同特征。本综述旨在从不同领域收集现有数据,并确定感应和随后清除受损溶酶体所需的关键步骤。最后我们将讨论疾病的影响,并重点关注神经退行性疾病。

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