p62/SQSTM1/A170: Physiology and pathology

被引:344
作者
Komatsu, Masaaki [1 ]
Kageyama, Shun [1 ]
Ichimura, Yoshinobu [1 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Prot Metab Project, Setagaya Ku, Tokyo 1568506, Japan
关键词
Autophagy; p62; LC3; mTORC1; Keap1; AUTOPHAGY-DEFICIENT MICE; TRANSCRIPTION FACTOR NRF2; SIGNALING ADAPTER P62; SELECTIVE AUTOPHAGY; PROTEIN AGGREGATION; CONJUGATION SYSTEM; STRESS-RESPONSE; PAGET-DISEASE; ACTIVATION; KEAP1;
D O I
10.1016/j.phrs.2012.07.004
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
p62/SQSTM1/A170 (hereafter referred to as p62) is a stress-inducible intracellular protein known to regulate various signal transduction pathways involved in cell survival and cell death. Comprehensive analysis of LC3 (an autophagosome localizing protein)-binding proteins resulted in the recognition of autophagy and p62. While autophagy modulates the level of p62 protein, p62 can suppress autophagy via activation of mTORC1. Moreover, growing lines of evidence point to the important role of p62 in directing ubiquitinated cargos toward autophagy as well as compaction of those cargos. Furthermore, this protein functions as a signaling hub for various signal transduction pathways, such as NF-kappa B signaling, apoptosis, and Nrf2 activation, whose dysregulation is associated with Paget disease of bone and tumorigenesis. In this review, we discuss the pathophysiological significance of p62 and its role in autophagy. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:457 / 462
页数:6
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