• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

p62 体:相分离、NRF2 激活和选择性自噬降解。

p62 bodies: Phase separation, NRF2 activation, and selective autophagic degradation.

机构信息

Department of Physiology, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

IUBMB Life. 2022 Dec;74(12):1200-1208. doi: 10.1002/iub.2689. Epub 2022 Nov 17.

DOI:10.1002/iub.2689
PMID:36331376
Abstract

When p62/Sequestosome-1 binds to a ubiquitinated protein, it undergoes liquid-liquid phase separation (LLPS) and forms a membraneless organelle, p62 body. There are two major physiological functions of the p62 body. One is effective autophagic degradation of ubiquitinated proteins and the other is antioxidant stress response, both of which contribute to cellular homeostasis. In this review, I review the history of p62 research in relation to autophagy and outline the formation, degradation, and physiological functions of the p62 body.

摘要

当 p62/自噬体相关蛋白 1(Sequestosome-1)与泛素化蛋白结合时,它会发生液-液相分离(LLPS)并形成无膜细胞器 p62 体。p62 体具有两个主要的生理功能。一个是有效降解泛素化蛋白的自噬作用,另一个是抗氧化应激反应,这两者都有助于细胞内的稳态。在这篇综述中,我回顾了与自噬相关的 p62 研究历史,并概述了 p62 体的形成、降解和生理功能。

相似文献

1
p62 bodies: Phase separation, NRF2 activation, and selective autophagic degradation.p62 体:相分离、NRF2 激活和选择性自噬降解。
IUBMB Life. 2022 Dec;74(12):1200-1208. doi: 10.1002/iub.2689. Epub 2022 Nov 17.
2
p62/SQSTM1 is a target gene for transcription factor NRF2 and creates a positive feedback loop by inducing antioxidant response element-driven gene transcription.p62/SQSTM1 是转录因子 NRF2 的靶基因,通过诱导抗氧化反应元件驱动的基因转录,形成正反馈回路。
J Biol Chem. 2010 Jul 16;285(29):22576-91. doi: 10.1074/jbc.M110.118976. Epub 2010 May 7.
3
NBR1-mediated p62-liquid droplets enhance the Keap1-Nrf2 system.NBR1 介导的 p62 液滴增强了 Keap1-Nrf2 系统。
EMBO Rep. 2020 Mar 4;21(3):e48902. doi: 10.15252/embr.201948902. Epub 2020 Jan 9.
4
Partial impairment of late-stage autophagic flux in murine splenocytes leads to sqstm1/p62 mediated nrf2-keap1 antioxidant pathway activation and induced proteasome-mediated degradation in malaria.在疟疾中,鼠脾细胞晚期自噬通量部分受损导致 sqstm1/p62 介导的 nrf2-keap1 抗氧化途径激活和诱导蛋白酶体介导的降解。
Microb Pathog. 2020 Oct;147:104289. doi: 10.1016/j.micpath.2020.104289. Epub 2020 Jul 18.
5
A noncanonical mechanism of Nrf2 activation by autophagy deficiency: direct interaction between Keap1 and p62.自噬缺陷激活 Nrf2 的非经典机制:Keap1 和 p62 之间的直接相互作用。
Mol Cell Biol. 2010 Jul;30(13):3275-85. doi: 10.1128/MCB.00248-10. Epub 2010 Apr 26.
6
p62 bodies: cytosolic zoning by phase separation.p62 体:相分离的细胞质分区。
J Biochem. 2024 Feb 25;175(2):141-146. doi: 10.1093/jb/mvad089.
7
SPOP mutations promote p62/SQSTM1-dependent autophagy and Nrf2 activation in prostate cancer.SPOP 突变促进前列腺癌中 p62/SQSTM1 依赖性自噬和 Nrf2 激活。
Cell Death Differ. 2022 Jun;29(6):1228-1239. doi: 10.1038/s41418-021-00913-w. Epub 2022 Jan 6.
8
MOAP-1-mediated dissociation of p62/SQSTM1 bodies releases Keap1 and suppresses Nrf2 signaling.MOAP-1 介导的 p62/SQSTM1 体解离释放 Keap1 并抑制 Nrf2 信号通路。
EMBO Rep. 2021 Jan 7;22(1):e50854. doi: 10.15252/embr.202050854. Epub 2021 Jan 4.
9
The selective autophagy substrate p62 activates the stress responsive transcription factor Nrf2 through inactivation of Keap1.选择性自噬底物 p62 通过失活 Keap1 激活应激反应转录因子 Nrf2。
Nat Cell Biol. 2010 Mar;12(3):213-23. doi: 10.1038/ncb2021. Epub 2010 Feb 21.
10
Phosphorylation of p62 activates the Keap1-Nrf2 pathway during selective autophagy.p62 的磷酸化在选择性自噬过程中激活 Keap1-Nrf2 通路。
Mol Cell. 2013 Sep 12;51(5):618-31. doi: 10.1016/j.molcel.2013.08.003. Epub 2013 Sep 5.

引用本文的文献

1
Post-Translational Modification of p62: Roles and Regulations in Autophagy.p62的翻译后修饰:自噬中的作用与调控
Cells. 2025 Jul 2;14(13):1016. doi: 10.3390/cells14131016.
2
ROS-mediated cell death and phase separation in gynecological malignancies.活性氧介导的妇科恶性肿瘤中的细胞死亡与相分离
Eur J Med Res. 2025 Jul 5;30(1):578. doi: 10.1186/s40001-025-02846-3.
3
KEAP1 retention in phase-separated p62 bodies drives liver damage under autophagy-deficient conditions.在自噬缺陷条件下,KEAP1滞留于相分离的p62小体中会导致肝损伤。
EMBO Rep. 2025 May 28. doi: 10.1038/s44319-025-00483-9.
4
Targeting GPX4 to Induce Ferroptosis Overcomes Chemoresistance Mediated by the PAX8-AS1/GPX4 Axis in Intrahepatic Cholangiocarcinoma.靶向GPX4诱导铁死亡可克服肝内胆管癌中PAX8-AS1/GPX4轴介导的化疗耐药性。
Adv Sci (Weinh). 2025 Aug;12(30):e01042. doi: 10.1002/advs.202501042. Epub 2025 May 20.
5
Autophagy Dysfunction and Neurodegeneration: Where Does It Go Wrong?自噬功能障碍与神经退行性变:问题出在哪里?
J Mol Biol. 2025 Sep 15;437(18):169219. doi: 10.1016/j.jmb.2025.169219. Epub 2025 May 16.
6
Autophagy inhibition enhances antifibrotic potential of placental mesenchymal stem cells of fetal origin via regulating TGF-β1 mediated protein degradation of HGF.自噬抑制通过调节转化生长因子-β1介导的肝细胞生长因子蛋白降解增强胎儿来源的胎盘间充质干细胞的抗纤维化潜能。
Sci Rep. 2025 Apr 21;15(1):13805. doi: 10.1038/s41598-025-97054-8.
7
Interferon-induced PARP14-mediated ADP-ribosylation in p62 bodies requires the ubiquitin-proteasome system.干扰素诱导的PARP14介导的p62小体中的ADP核糖基化需要泛素-蛋白酶体系统。
EMBO J. 2025 May;44(10):2741-2773. doi: 10.1038/s44318-025-00421-4. Epub 2025 Apr 7.
8
ROCK1 promotes B cell differentiation and proteostasis under stress through the heme-regulated proteins, BACH2 and HRI.ROCK1通过血红素调节蛋白BACH2和HRI在应激条件下促进B细胞分化和蛋白质稳态。
JCI Insight. 2025 Feb 4;10(5):e180507. doi: 10.1172/jci.insight.180507.
9
Inhibition of SQSTM1/p62 oligomerization and Keap1 sequestration by the Cullin-3 adaptor SHKBP1.通过Cullin-3衔接蛋白SHKBP1抑制SQSTM1/p62寡聚化和Keap1隔离
bioRxiv. 2025 Jan 22:2025.01.21.634088. doi: 10.1101/2025.01.21.634088.
10
Fucoidan Oligosaccharide Supplementation Relieved Kidney Injury and Modulated Intestinal Homeostasis in D-Galactose-Exposed Rats.岩藻依聚糖寡糖补充剂可缓解 D-半乳糖诱导的大鼠肾损伤并调节肠道稳态。
Nutrients. 2025 Jan 17;17(2):325. doi: 10.3390/nu17020325.