• 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

线粒体自噬起始阶段的动态变化。

The dynamics of mitochondrial autophagy at the initiation stage.

机构信息

Signalling Programme, Babraham Institute, Cambridge CB22 3AT, U.K.

出版信息

Biochem Soc Trans. 2021 Nov 1;49(5):2199-2210. doi: 10.1042/BST20210272.

DOI:10.1042/BST20210272
PMID:34665253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8589415/
Abstract

The pathway of mitochondrial-specific autophagy (mitophagy, defined here as the specific elimination of mitochondria following distinct mitochondrial injuries or developmental/metabolic alterations) is important in health and disease. This review will be focussed on the earliest steps of the pathway concerning the mechanisms and requirements for initiating autophagosome formation on a mitochondrial target. More specifically, and in view of the fact that we understand the basic mechanism of non-selective autophagy and are beginning to reshape this knowledge towards the pathways of selective autophagy, two aspects of mitophagy will be covered: (i) How does a machinery normally working in association with the endoplasmic reticulum (ER) to make an autophagosome can also do so at a site distinct from the ER such as on the surface of the targeted cargo? and (ii) how does the machinery deal with cargo of multiple sizes?

摘要

线粒体特异性自噬(mitophagy,这里定义为在特定的线粒体损伤或发育/代谢改变后,线粒体的特异性消除)途径在健康和疾病中很重要。本综述将集中讨论该途径的早期步骤,涉及启动针对线粒体靶标的自噬体形成的机制和要求。更具体地说,鉴于我们已经了解了非选择性自噬的基本机制,并开始将这方面的知识重塑为选择性自噬途径,本文将涵盖 mitophagy 的两个方面:(i)正常与内质网(ER)结合以形成自噬体的机制如何也能在 ER 之外的特定部位(如靶向货物的表面)发挥作用?(ii)该机制如何处理不同大小的货物?

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/7e8c0e8d49db/BST-49-2199-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/dd329a5f976d/BST-49-2199-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/79c344306d53/BST-49-2199-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/c0ed0e6fd0db/BST-49-2199-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/7e8c0e8d49db/BST-49-2199-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/dd329a5f976d/BST-49-2199-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/79c344306d53/BST-49-2199-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/c0ed0e6fd0db/BST-49-2199-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e00/8589415/7e8c0e8d49db/BST-49-2199-g0004.jpg

相似文献

1
The dynamics of mitochondrial autophagy at the initiation stage.线粒体自噬起始阶段的动态变化。
Biochem Soc Trans. 2021 Nov 1;49(5):2199-2210. doi: 10.1042/BST20210272.
2
PINK1 and BECN1 relocalize at mitochondria-associated membranes during mitophagy and promote ER-mitochondria tethering and autophagosome formation.在细胞自噬过程中,PINK1和BECN1在线粒体相关膜上重新定位,并促进内质网与线粒体的连接以及自噬体的形成。
Autophagy. 2017 Apr 3;13(4):654-669. doi: 10.1080/15548627.2016.1277309. Epub 2017 Feb 17.
3
Selective Autophagy of Mitochondria on a Ubiquitin-Endoplasmic-Reticulum Platform.泛素-内质网平台上的线粒体选择性自噬。
Dev Cell. 2019 Sep 9;50(5):627-643.e5. doi: 10.1016/j.devcel.2019.06.016. Epub 2019 Jul 25.
4
SIGMAR1/Sigma-1 receptor ablation impairs autophagosome clearance.SIGMAR1/Sigma-1 受体缺失会损害自噬体的清除。
Autophagy. 2019 Sep;15(9):1539-1557. doi: 10.1080/15548627.2019.1586248. Epub 2019 Mar 14.
5
FUNDC1 alleviates doxorubicin-induced cardiotoxicity by restoring mitochondrial-endoplasmic reticulum contacts and blocked autophagic flux.FUNDC1 通过恢复线粒体-内质网接触和阻断自噬通量来减轻阿霉素诱导的心脏毒性。
Theranostics. 2024 Jun 17;14(9):3719-3738. doi: 10.7150/thno.92771. eCollection 2024.
6
Targeted siRNA Screens Identify ER-to-Mitochondrial Calcium Exchange in Autophagy and Mitophagy Responses in RPE1 Cells.靶向siRNA筛选鉴定RPE1细胞自噬和线粒体自噬反应中内质网到线粒体的钙交换
Int J Mol Sci. 2015 Jun 11;16(6):13356-80. doi: 10.3390/ijms160613356.
7
Evidence for the involvement of lipid rafts localized at the ER-mitochondria associated membranes in autophagosome formation.内质网-线粒体相关膜上定位的脂筏参与自噬体形成的证据。
Autophagy. 2016 Jun 2;12(6):917-35. doi: 10.1080/15548627.2016.1160971. Epub 2016 Apr 28.
8
Amyloid Β-Peptide Increases Mitochondria-Endoplasmic Reticulum Contact Altering Mitochondrial Function and Autophagosome Formation in Alzheimer's Disease-Related Models.淀粉样β肽增加线粒体与内质网的接触,改变阿尔茨海默病相关模型中的线粒体功能和自噬体形成。
Cells. 2020 Nov 28;9(12):2552. doi: 10.3390/cells9122552.
9
BHRF1, a BCL2 viral homolog, disturbs mitochondrial dynamics and stimulates mitophagy to dampen type I IFN induction.BHRF1,一种 BCL2 病毒同源物,扰乱线粒体动力学并刺激线粒体自噬,以抑制 I 型 IFN 的诱导。
Autophagy. 2021 Jun;17(6):1296-1315. doi: 10.1080/15548627.2020.1758416. Epub 2020 May 13.
10
Diverse Cellular Roles of Autophagy.自噬的多种细胞作用
Annu Rev Cell Dev Biol. 2019 Oct 6;35:453-475. doi: 10.1146/annurev-cellbio-100818-125300. Epub 2019 Jul 5.

引用本文的文献

1
Manipulating autophagic degradation in human diseases: from mechanisms to interventions.调控人类疾病中的自噬降解:从机制到干预措施
Life Med. 2022 Oct 11;1(2):120-148. doi: 10.1093/lifemedi/lnac043. eCollection 2022 Oct.
2
Nucleus-Mitochondria Contact Sites Are Associated With Asynthetic Fission in Zebrafish Skin.细胞核-线粒体接触位点与斑马鱼皮肤中的非同步裂变相关。
Contact (Thousand Oaks). 2024 Mar 14;7:25152564241239445. doi: 10.1177/25152564241239445. eCollection 2024 Jan-Dec.
3
Buyang Huanwu Decoction alleviates cerebral ischemic injury through modulating caveolin-1-mediated mitochondrial quality control.

本文引用的文献

1
Distinct fission signatures predict mitochondrial degradation or biogenesis.独特的裂变特征可预测线粒体的降解或生物发生。
Nature. 2021 May;593(7859):435-439. doi: 10.1038/s41586-021-03510-6. Epub 2021 May 5.
2
Membrane supply and remodeling during autophagosome biogenesis.自噬体生物发生过程中的膜供应和重塑。
Curr Opin Cell Biol. 2021 Aug;71:112-119. doi: 10.1016/j.ceb.2021.02.001. Epub 2021 Apr 27.
3
ATG4 family proteins drive phagophore growth independently of the LC3/GABARAP lipidation system.ATG4 家族蛋白独立于 LC3/GABARAP 脂质化系统驱动噬泡生长。
补阳还五汤通过调节小窝蛋白-1介导的线粒体质量控制减轻脑缺血损伤。
Front Pharmacol. 2023 May 10;14:1137609. doi: 10.3389/fphar.2023.1137609. eCollection 2023.
4
Structural basis for ATG9A recruitment to the ULK1 complex in mitophagy initiation.自噬起始中 ATG9A 招募到 ULK1 复合物的结构基础。
Sci Adv. 2023 Feb 15;9(7):eadg2997. doi: 10.1126/sciadv.adg2997.
5
Mitophagy in the aging nervous system.衰老神经系统中的线粒体自噬
Front Cell Dev Biol. 2022 Oct 11;10:978142. doi: 10.3389/fcell.2022.978142. eCollection 2022.
Mol Cell. 2021 May 6;81(9):2013-2030.e9. doi: 10.1016/j.molcel.2021.03.001. Epub 2021 Mar 26.
4
Regulation of PRKN-independent mitophagy.PRKN 非依赖性线粒体自噬的调控。
Autophagy. 2022 Jan;18(1):24-39. doi: 10.1080/15548627.2021.1888244. Epub 2021 Feb 25.
5
Wetting regulates autophagy of phase-separated compartments and the cytosol.湿润调节相分离隔室和细胞质的自噬。
Nature. 2021 Mar;591(7848):142-146. doi: 10.1038/s41586-020-2992-3. Epub 2021 Jan 20.
6
Biomolecular condensates in autophagy regulation.自噬调控中的生物分子凝聚物。
Curr Opin Cell Biol. 2021 Apr;69:23-29. doi: 10.1016/j.ceb.2020.12.011. Epub 2021 Jan 11.
7
Molecular mechanisms and physiological functions of mitophagy.线粒体自噬的分子机制和生理功能。
EMBO J. 2021 Feb 1;40(3):e104705. doi: 10.15252/embj.2020104705. Epub 2021 Jan 13.
8
p62/SQSTM1-droplet serves as a platform for autophagosome formation and anti-oxidative stress response.p62/SQSTM1 液滴可作为自噬体形成和抗氧化应激反应的平台。
Nat Commun. 2021 Jan 4;12(1):16. doi: 10.1038/s41467-020-20185-1.
9
A framework for understanding the functions of biomolecular condensates across scales.理解生物分子凝聚物在不同尺度上功能的框架。
Nat Rev Mol Cell Biol. 2021 Mar;22(3):215-235. doi: 10.1038/s41580-020-00303-z. Epub 2020 Nov 9.
10
Structure, lipid scrambling activity and role in autophagosome formation of ATG9A.ATG9A 的结构、脂质翻转活性及其在自噬体形成中的作用。
Nat Struct Mol Biol. 2020 Dec;27(12):1194-1201. doi: 10.1038/s41594-020-00520-2. Epub 2020 Oct 26.