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p62的相分离:自噬中的作用与调控

Phase separation of p62: roles and regulations in autophagy.

作者信息

Huang Xue, Zhang Jinpei, Yao Jia, Mi Na, Yang Aimin

机构信息

School of Life Sciences, Chongqing University, Chongqing 401331, China; Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing 400016, China.

State Key Laboratory of Pathogenesis, Prevention and Treatment of Central Asian High Incidence Diseases, Clinical Medical Research Institute, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang, China; Basic Medical College, Xinjiang Medical University, Urumqi, 830011, Xinjiang, China; Key Laboratory of High Incidence Disease Research in Xinjiang (Xinjiang Medical University), Ministry of Education, Urumqi, 830011, Xinjiang, China.

出版信息

Trends Cell Biol. 2025 Feb 25. doi: 10.1016/j.tcb.2025.01.010.

Abstract

The phase separation of the cargo receptor sequestome-1/p62 (SQSTM1/p62) is a critical mechanism for assembling signaling complexes in autophagy. During this process, p62 undergoes phase separation upon binding to polyubiquitin chains, concentrating ubiquitinated substrates within p62 droplets. These droplets further gather membrane sources and core autophagy machineries to facilitate autophagosome formation. The dynamics of p62 droplets are finely tuned in response to autophagy signals triggered by cellular stresses. Recent studies have revealed new regulatory mechanisms that highlight the significance of p62 phase separation in regulating autophagy. This review summarizes and discusses the molecular mechanisms of p62 phase separation and its roles in autophagy, with particular emphasis on the regulation of p62 droplets and their interaction modes with autophagic membranes.

摘要

货物受体隔离蛋白1/p62(SQSTM1/p62)的相分离是自噬中组装信号复合物的关键机制。在此过程中,p62与多聚泛素链结合后发生相分离,将泛素化底物浓缩在p62液滴内。这些液滴进一步聚集膜源和核心自噬机制,以促进自噬体形成。p62液滴的动态变化会根据细胞应激触发的自噬信号进行精细调节。最近的研究揭示了新的调控机制,突出了p62相分离在调节自噬中的重要性。本综述总结并讨论了p62相分离的分子机制及其在自噬中的作用,特别强调了p62液滴的调控及其与自噬膜的相互作用模式。

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