• 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

相似文献

1
PHB2 (prohibitin 2) promotes PINK1-PRKN/Parkin-dependent mitophagy by the PARL-PGAM5-PINK1 axis.PHB2(抑制素 2)通过 PARL-PGAM5-PINK1 轴促进 PINK1-PRKN/Parkin 依赖性线粒体自噬。
Autophagy. 2020 Mar;16(3):419-434. doi: 10.1080/15548627.2019.1628520. Epub 2019 Jun 16.
2
mutations impair depolarization-induced mitophagy through inhibition of mitochondrial accumulation of RAB10.突变通过抑制 RAB10 在线粒体中的积累来损害去极化诱导的线粒体自噬。
Autophagy. 2020 Feb;16(2):203-222. doi: 10.1080/15548627.2019.1603548. Epub 2019 Apr 19.
3
PGAM5 regulates PINK1/Parkin-mediated mitophagy via DRP1 in CCCP-induced mitochondrial dysfunction.PGAM5通过动力相关蛋白1(DRP1)在CCCP诱导的线粒体功能障碍中调节PINK1/帕金蛋白介导的线粒体自噬。
Toxicol Lett. 2018 Mar 1;284:120-128. doi: 10.1016/j.toxlet.2017.12.004. Epub 2017 Dec 11.
4
Spautin-1 promotes PINK1-PRKN-dependent mitophagy and improves associative learning capability in an alzheimer disease animal model.Spautin-1 促进 PINK1-PRKN 依赖性线粒体自噬,并改善阿尔茨海默病动物模型中的联想学习能力。
Autophagy. 2024 Dec;20(12):2655-2676. doi: 10.1080/15548627.2024.2383145. Epub 2024 Aug 1.
5
Organelle-specific autophagy in inflammatory diseases: a potential therapeutic target underlying the quality control of multiple organelles.炎症性疾病中的细胞器特异性自噬:多种细胞器质量控制的潜在治疗靶点。
Autophagy. 2021 Feb;17(2):385-401. doi: 10.1080/15548627.2020.1725377. Epub 2020 Feb 12.
6
Alternative mitochondrial quality control mediated by extracellular release.通过细胞外释放实现的替代性线粒体质量控制。
Autophagy. 2021 Oct;17(10):2962-2974. doi: 10.1080/15548627.2020.1848130. Epub 2020 Dec 10.
7
PRKN-regulated mitophagy and cellular senescence during COPD pathogenesis.PRKN 调控的细胞自噬和细胞衰老在 COPD 发病机制中的作用。
Autophagy. 2019 Mar;15(3):510-526. doi: 10.1080/15548627.2018.1532259. Epub 2018 Oct 13.
8
Prohibitins, Phb1 and Phb2, function as Atg8 receptors to support yeast mitophagy and also play a negative regulatory role in Atg32 processing.抑素蛋白 Phb1 和 Phb2 作为 Atg8 的受体,在支持酵母线粒体自噬中发挥作用,同时在 Atg32 加工中起负调控作用。
Autophagy. 2024 Nov;20(11):2478-2489. doi: 10.1080/15548627.2024.2371717. Epub 2024 Jul 4.
9
Increased mitophagy protects cochlear hair cells from aminoglycoside-induced damage.增强的线粒体自噬可保护耳蜗毛细胞免受氨基糖苷类药物诱导的损伤。
Autophagy. 2023 Jan;19(1):75-91. doi: 10.1080/15548627.2022.2062872. Epub 2022 Apr 26.
10
Syntaxin 17 regulates the localization and function of PGAM5 in mitochondrial division and mitophagy.Syntaxin 17 调节 PGAM5 在线粒体分裂和线粒体自噬中的定位和功能。
EMBO J. 2018 Nov 2;37(21). doi: 10.15252/embj.201798899. Epub 2018 Sep 20.

引用本文的文献

1
Mitophagy in kidney transplantation ischemia-reperfusion injury.肾移植缺血再灌注损伤中的线粒体自噬
Int Urol Nephrol. 2025 Sep 1. doi: 10.1007/s11255-025-04761-2.
2
Mitochondrial quality control in diabetes mellitus and complications: molecular mechanisms and therapeutic strategies.糖尿病及其并发症中的线粒体质量控制:分子机制与治疗策略
Cell Death Dis. 2025 Aug 27;16(1):652. doi: 10.1038/s41419-025-07936-y.
3
Research progress on programmed cell death of cardiomyocytes in pressure-overload hypertrophic cardiomyopathy.压力超负荷肥厚型心肌病中心肌细胞程序性细胞死亡的研究进展
Apoptosis. 2025 Aug 14. doi: 10.1007/s10495-025-02146-5.
4
Mitochondrial echoes in the bloodstream: decoding ccf-mtDNA for the early detection and prognosis of hepatocellular carcinoma.血液中的线粒体回声:解码循环游离线粒体DNA用于肝细胞癌的早期检测和预后评估
Cell Biosci. 2025 Aug 12;15(1):118. doi: 10.1186/s13578-025-01456-0.
5
In situ cryo-ET visualization of mitochondrial depolarization and mitophagic engulfment.线粒体去极化和线粒体自噬吞噬的原位冷冻电镜观察
Proc Natl Acad Sci U S A. 2025 Aug 5;122(31):e2511890122. doi: 10.1073/pnas.2511890122. Epub 2025 Jul 31.
6
Perspectives on mitochondrial dysfunction in the regeneration of aging skeletal muscle.衰老骨骼肌再生中线粒体功能障碍的研究视角
Cell Mol Biol Lett. 2025 Jul 28;30(1):94. doi: 10.1186/s11658-025-00771-1.
7
Mitophagy related gene signature for prognosis and therapeutic evaluation in KIRC.肾透明细胞癌中用于预后和治疗评估的线粒体自噬相关基因特征
Sci Rep. 2025 Jul 26;15(1):27273. doi: 10.1038/s41598-025-10798-1.
8
PHB2 protects against pressure overload-induced myocardial remodeling in mice via stabilizing TOMM40 and regulating mitochondrial morphofunctional homeostasis.PHB2通过稳定TOMM40和调节线粒体形态功能稳态来保护小鼠免受压力超负荷诱导的心肌重塑。
Acta Pharmacol Sin. 2025 Jul 14. doi: 10.1038/s41401-025-01613-8.
9
Mechanism and regulation of mitophagy in liver diseases: a review.肝脏疾病中细胞自噬的机制与调控:综述
Front Cell Dev Biol. 2025 Jun 27;13:1614940. doi: 10.3389/fcell.2025.1614940. eCollection 2025.
10
Structures and functions of the MICOS: Pathogenesis and therapeutic implications in Alzheimer's disease.线粒体接触位点和嵴组织系统(MICOS)的结构与功能:在阿尔茨海默病中的发病机制及治疗意义
Acta Pharm Sin B. 2025 Jun;15(6):2966-2984. doi: 10.1016/j.apsb.2025.04.019. Epub 2025 Apr 22.

本文引用的文献

1
Sam50 Regulates PINK1-Parkin-Mediated Mitophagy by Controlling PINK1 Stability and Mitochondrial Morphology.Sam50 通过控制 PINK1 稳定性和线粒体形态来调节 PINK1-Parkin 介导的线粒体自噬。
Cell Rep. 2018 Jun 5;23(10):2989-3005. doi: 10.1016/j.celrep.2018.05.015.
2
PINK1 import regulation; a fine system to convey mitochondrial stress to the cytosol.PINK1 输入调控;将线粒体应激传递到细胞质的精细系统。
BMC Biol. 2018 Jan 10;16(1):2. doi: 10.1186/s12915-017-0470-7.
3
Prohibitin-2 negatively regulates AKT2 expression to promote prostate cancer cell migration.抑素-2 负调控 AKT2 的表达以促进前列腺癌细胞迁移。
Int J Mol Med. 2018 Feb;41(2):1147-1155. doi: 10.3892/ijmm.2017.3307. Epub 2017 Dec 4.
4
Targeting prohibitins with chemical ligands inhibits KRAS-mediated lung tumours.用化学配体靶向抑制素可抑制KRAS介导的肺癌。
Oncogene. 2017 Oct 19;36(42):5914. doi: 10.1038/onc.2017.307. Epub 2017 Aug 28.
5
A fluorescence-based imaging method to measure in vitro and in vivo mitophagy using mt-Keima.一种基于荧光的成像方法,用于使用 mt-Keima 测量体外和体内的线粒体自噬。
Nat Protoc. 2017 Aug;12(8):1576-1587. doi: 10.1038/nprot.2017.060. Epub 2017 Jul 13.
6
Prohibitins.抑制素。
Curr Biol. 2017 Jul 10;27(13):R629-R631. doi: 10.1016/j.cub.2017.04.030.
7
Mitophagy: Link to cancer development and therapy.线粒体自噬:与癌症发展和治疗的关联
Biochem Biophys Res Commun. 2017 Jan 15;482(3):432-439. doi: 10.1016/j.bbrc.2016.10.088. Epub 2017 Feb 3.
8
The pharmacological regulation of cellular mitophagy.细胞线粒体自噬的药理学调控。
Nat Chem Biol. 2017 Jan 19;13(2):136-146. doi: 10.1038/nchembio.2287.
9
Prohibitin 2 Is an Inner Mitochondrial Membrane Mitophagy Receptor. prohibitin 2是一种线粒体内膜线粒体自噬受体。
Cell. 2017 Jan 12;168(1-2):224-238.e10. doi: 10.1016/j.cell.2016.11.042. Epub 2016 Dec 22.
10
The membrane scaffold SLP2 anchors a proteolytic hub in mitochondria containing PARL and the i-AAA protease YME1L.膜支架蛋白SLP2在含有PARL和i-AAA蛋白酶YME1L的线粒体中锚定一个蛋白水解中心。
EMBO Rep. 2016 Dec;17(12):1844-1856. doi: 10.15252/embr.201642698. Epub 2016 Oct 13.

PHB2(抑制素 2)通过 PARL-PGAM5-PINK1 轴促进 PINK1-PRKN/Parkin 依赖性线粒体自噬。

PHB2 (prohibitin 2) promotes PINK1-PRKN/Parkin-dependent mitophagy by the PARL-PGAM5-PINK1 axis.

机构信息

Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, Hubei, PR. China.

Faculty of Pharmacy, University of Strasbourg-CNRS, Illkirch, France.

出版信息

Autophagy. 2020 Mar;16(3):419-434. doi: 10.1080/15548627.2019.1628520. Epub 2019 Jun 16.

DOI:10.1080/15548627.2019.1628520
PMID:31177901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6999623/
Abstract

Mitophagy, which is a conserved cellular process for selectively removing damaged or unwanted mitochondria, is critical for mitochondrial quality control and the maintenance of normal cellular physiology. However, the precise mechanisms underlying mitophagy remain largely unknown. Prior studies on mitophagy focused on the events in the mitochondrial outer membrane. PHB2 (prohibitin 2), which is a highly conserved membrane scaffold protein, was recently identified as a novel inner membrane mitophagy receptor that mediates mitophagy. Here, we report a new signaling pathway for PHB2-mediated mitophagy. Upon mitochondrial membrane depolarization or misfolded protein aggregation, PHB2 depletion destabilizes PINK1 in the mitochondria, which blocks the mitochondrial recruitment of PRKN/Parkin, ubiquitin and OPTN (optineurin), leading to an inhibition of mitophagy. In addition, PHB2 overexpression directly induces PRKN recruitment to the mitochondria. Moreover, PHB2-mediated mitophagy is dependent on the mitochondrial inner membrane protease PARL, which interacts with PHB2 and is activated upon PHB2 depletion. Furthermore, PGAM5, which is processed by PARL, participates in PHB2-mediated PINK1 stabilization. Finally, a ligand of PHB proteins that we synthesized, called FL3, was found to strongly inhibit PHB2-mediated mitophagy and to effectively block cancer cell growth and energy production at nanomolar concentrations. Thus, our findings reveal that the PHB2-PARL-PGAM5-PINK1 axis is a novel pathway of PHB2-mediated mitophagy and that targeting PHB2 with the chemical compound FL3 is a promising strategy for cancer therapy.: AIFM1: apoptosis inducing factor mitochondria associated 1; ATP5F1A/ATP5A1: ATP synthase F1 subunit alpha; BAF: bafilomycin A; CALCOCO2/NDP52: calcium binding and coiled-coil domain 2; CCCP: chemical reagent carbonyl cyanide m-chlorophenyl hydrazine; FL3: flavaglines compound 3; HSPD1/HSP60: heat shock protein family D (Hsp60) member 1; LC3B/MAP1LC3B: microtubule associated protein 1 light chain 3 beta; MEF: mouse embryo fibroblasts; MPP: mitochondrial-processing peptidase; MT-CO2/COX2: mitochondrially encoded cytochrome c oxidase II; MTS: mitochondrial targeting sequence; OA: oligomycin and antimycin A; OPTN: optineurin; OTC: ornithine carbamoyltransferase; PARL: presenilin associated rhomboid like; PBS: phosphate-buffered saline; PGAM5: PGAM family member 5, mitochondrial serine/threonine protein phosphatase; PHB: prohibitin; PHB2: prohibitin 2; PINK1: PTEN induced kinase 1; PRKN/Parkin: parkin RBR E3 ubiquitin protein ligase; Roc-A: rocaglamide A; TOMM20: translocase of outer mitochondrial membrane 20; TUBB: tubulin beta class I.

摘要

自噬,一种选择性清除受损或不需要的线粒体的保守细胞过程,对于线粒体质量控制和维持正常细胞生理功能至关重要。然而,自噬的确切机制在很大程度上仍然未知。先前的自噬研究主要集中在线粒体外膜的事件上。PHB2(阻遏素 2),一种高度保守的膜支架蛋白,最近被鉴定为一种新的内膜自噬受体,介导自噬。在这里,我们报告了一个新的 PHB2 介导的自噬信号通路。在线粒体去极化或错误折叠的蛋白质聚集时,PHB2 的耗竭会使 PINK1 在线粒体中不稳定,从而阻止 PRKN/Parkin、泛素和 OPTN(optineurin)在线粒体上的募集,从而抑制自噬。此外,PHB2 的过表达直接诱导 PRKN 向线粒体的募集。此外,PHB2 介导的自噬依赖于线粒体内膜蛋白酶 PARL,PARL 与 PHB2 相互作用,并在 PHB2 耗竭时被激活。此外,PGAM5,一种被 PARL 加工的蛋白,参与 PHB2 介导的 PINK1 稳定。最后,我们合成了一种 PHB 蛋白的配体,称为 FL3,发现它强烈抑制 PHB2 介导的自噬,并以纳摩尔浓度有效地阻断癌细胞的生长和能量产生。因此,我们的研究结果表明,PHB2-PARL-PGAM5-PINK1 轴是 PHB2 介导的自噬的一个新途径,用化学化合物 FL3 靶向 PHB2 是癌症治疗的一种很有前途的策略。AIFM1:凋亡诱导因子线粒体相关 1;ATP5F1A/ATP5A1:ATP 合酶 F1 亚基 alpha;BAF:巴弗霉素 A;CALCOCO2/NDP52:钙结合和卷曲螺旋结构域 2;CCCP:化学试剂羰基氰化物 m-氯苯腙;FL3:flavaglines 化合物 3;HSPD1/HSP60:热休克蛋白家族 D(Hsp60)成员 1;LC3B/MAP1LC3B:微管相关蛋白 1 轻链 3 beta;MEF:鼠胚胎成纤维细胞;MPP:线粒体加工肽酶;MT-CO2/COX2:线粒体编码细胞色素 c 氧化酶 II;MTS:线粒体靶向序列;OA:寡霉素和抗霉素 A;OPTN:optineurin;OTC:鸟氨酸氨甲酰转移酶;PARL:早老素相关的类环指蛋白;PBS:磷酸盐缓冲盐水;PGAM5:PGAM 家族成员 5,线粒体丝氨酸/苏氨酸蛋白磷酸酶;PHB:阻遏素;PHB2:阻遏素 2;PINK1:PTEN 诱导的激酶 1;PRKN/Parkin:Parkin RBR E3 泛素蛋白连接酶;Roc-A:rocaglamide A;TOMM20:外线粒体膜转运蛋白 20;TUBB:微管蛋白 beta 类 I。