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自噬及溶酶体介导的蛋白质降解相关机制

Autophagy and related mechanisms of lysosome-mediated protein degradation.

作者信息

Dunn W A

机构信息

Department of Anatomy and Cell Biology, Box 100235, JHMHC, University of Florida College of Medicine, Gainesville, FL 32610, USA.

出版信息

Trends Cell Biol. 1994 Apr;4(4):139-43. doi: 10.1016/0962-8924(94)90069-8.

Abstract

Lysosomes play a central role in the degradation of extracellular and intracellular macromolecules. These organelles contain hydrolytic enzymes capable of degrading proteins, proteoglycans, nucleic acids, and lipids. The mechanisms involved in the delivery of such intracellular compounds to the lysosome have been characterized in several recent studies. The sequestration of intracellular macromolecules for intralysosomal degradation can occur by crinophagy, hsc73-mediated carrier transport, or autophagy. The major route of delivery of cellular proteins and RNA into lysosomes is by autophagy. Furthermore, autophagy is regulated by nutrients and hormones, thus allowing the cell to adjust its degradative state to environmental changes.

摘要

溶酶体在细胞外和细胞内大分子的降解过程中发挥着核心作用。这些细胞器含有能够降解蛋白质、蛋白聚糖、核酸和脂质的水解酶。最近的几项研究已经阐明了将此类细胞内化合物运输到溶酶体的机制。细胞内大分子被隔离用于溶酶体内降解可通过分泌自噬、热休克蛋白73(hsc73)介导的载体转运或自噬发生。细胞蛋白质和RNA进入溶酶体的主要途径是自噬。此外,自噬受营养物质和激素的调节,从而使细胞能够根据环境变化调整其降解状态。

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