• 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

当溶酶体老化时。

When lysosomes get old.

作者信息

Cuervo A M, Dice J F

机构信息

Department of Physiology, Tufts University School of Medicine, Boston, MA, USA.

出版信息

Exp Gerontol. 2000 Mar;35(2):119-31. doi: 10.1016/s0531-5565(00)00075-9.

DOI:10.1016/s0531-5565(00)00075-9
PMID:10767573
Abstract

Changes in the lysosomes of senescent tissues and organisms are common and have been used as biomarkers of aging. Lysosomes are responsible for the degradation of many macromolecules, including proteins. At least five different pathways for the delivery of substrate proteins to lysosomes are known. Three of these pathways decline with age, and the molecular explanations for these deficiencies are currently being studied. Other aspects of lysosomal proteolysis increase or do not change with age in spite of marked changes in lysosomal morphology and biochemistry. Age-related changes in certain lysosomal pathways of proteolysis remain to be studied. This area of research is important because abnormalities in lysosomal protein degradation pathways may contribute to several characteristics and pathologies associated with aging.

摘要

衰老组织和生物体的溶酶体变化很常见,并且已被用作衰老的生物标志物。溶酶体负责许多大分子的降解,包括蛋白质。已知至少有五种不同的将底物蛋白递送至溶酶体的途径。其中三种途径会随着年龄增长而衰退,目前正在研究这些缺陷的分子解释。尽管溶酶体形态和生物化学发生了显著变化,但溶酶体蛋白水解的其他方面随年龄增长而增加或没有变化。某些溶酶体蛋白水解途径中与年龄相关的变化仍有待研究。这一研究领域很重要,因为溶酶体蛋白降解途径的异常可能导致与衰老相关的几种特征和病理状况。

相似文献

1
When lysosomes get old.当溶酶体老化时。
Exp Gerontol. 2000 Mar;35(2):119-31. doi: 10.1016/s0531-5565(00)00075-9.
2
How do intracellular proteolytic systems change with age?细胞内蛋白水解系统如何随年龄变化?
Front Biosci. 1998 Jan 1;3:d25-43. doi: 10.2741/a264.
3
Microinjected ribonuclease A as a probe for lysosomal pathways of intracellular protein degradation.显微注射的核糖核酸酶A作为细胞内蛋白质降解溶酶体途径的探针。
J Protein Chem. 1988 Apr;7(2):115-27. doi: 10.1007/BF01025241.
4
Altered intracellular protein degradation in aging: a possible cause of proliferative arrest.衰老过程中细胞内蛋白质降解的改变:增殖停滞的一个可能原因。
Exp Gerontol. 1989;24(5-6):451-9. doi: 10.1016/0531-5565(89)90051-x.
5
Altered dynamics of the lysosomal receptor for chaperone-mediated autophagy with age.伴侣蛋白介导的自噬的溶酶体受体动力学随年龄改变。
J Cell Sci. 2007 Mar 1;120(Pt 5):782-91. doi: 10.1242/jcs.001073. Epub 2007 Feb 6.
6
[Influence of delta-sleep inducing peptide on the state of lysosomal membranes and intensity of lysosomal proteolysis in different rat tissues during physiological aging of the organism].[δ-睡眠诱导肽对机体生理衰老过程中不同大鼠组织溶酶体膜状态及溶酶体蛋白水解强度的影响]
Adv Gerontol. 2014;27(3):488-95.
7
Activation of a selective pathway of lysosomal proteolysis in rat liver by prolonged starvation.长期饥饿对大鼠肝脏溶酶体蛋白水解选择性途径的激活作用。
Am J Physiol. 1995 Nov;269(5 Pt 1):C1200-8. doi: 10.1152/ajpcell.1995.269.5.C1200.
8
Lysosomal metabolism of glycoproteins.糖蛋白的溶酶体代谢
Glycobiology. 2005 Jun;15(6):1R-15R. doi: 10.1093/glycob/cwi041. Epub 2005 Jan 12.
9
Targeting specific proteins for lysosomal proteolysis.
Biomed Biochim Acta. 1991;50(4-6):393-7.
10
Bioremediation meets biomedicine: therapeutic translation of microbial catabolism to the lysosome.生物修复与生物医学相遇:微生物分解代谢向溶酶体的治疗性转化。
Trends Biotechnol. 2002 Nov;20(11):452-5. doi: 10.1016/s0167-7799(02)02062-0.

引用本文的文献

1
Sit4 Genetically Interacts with Vps27 to Regulate Mitochondrial Function and Lifespan in .Sit4 与 Vps27 相互作用,调节. 中的线粒体功能和寿命。
Cells. 2024 Apr 9;13(8):655. doi: 10.3390/cells13080655.
2
The influencer effect of Dexmedetomidine on radioiodine relevant to lacrimal gland impairment.右美托咪定对放射性碘相关泪腺损伤的影响的影响者效应。
Int Ophthalmol. 2024 Feb 27;44(1):115. doi: 10.1007/s10792-024-03052-6.
3
Lysosomes in senescence and aging.衰老和老化中的溶酶体。
EMBO Rep. 2023 Nov 6;24(11):e57265. doi: 10.15252/embr.202357265. Epub 2023 Oct 9.
4
The Multifaceted Role of WNT Signaling in Alzheimer's Disease Onset and Age-Related Progression.WNT 信号在阿尔茨海默病发病和与年龄相关进展中的多方面作用。
Cells. 2023 Apr 21;12(8):1204. doi: 10.3390/cells12081204.
5
Proteostasis in aging-associated ocular disease.衰老相关眼病中的蛋白稳态。
Mol Aspects Med. 2022 Dec;88:101157. doi: 10.1016/j.mam.2022.101157. Epub 2022 Nov 29.
6
Oligodendroglial macroautophagy is essential for myelin sheath turnover to prevent neurodegeneration and death.少突胶质细胞巨自噬对于髓鞘鞘更替以防止神经退行性变和死亡是必需的。
Cell Rep. 2022 Oct 18;41(3):111480. doi: 10.1016/j.celrep.2022.111480.
7
Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies.继发性线粒体功能障碍作为溶酶体贮积病神经退行性功能障碍的病因,以及潜在治疗方法概述。
Int J Mol Sci. 2022 Sep 12;23(18):10573. doi: 10.3390/ijms231810573.
8
Proteolysis dysfunction in the process of aging and age-related diseases.衰老及与年龄相关疾病过程中的蛋白水解功能障碍。
Front Aging. 2022 Jul 22;3:927630. doi: 10.3389/fragi.2022.927630. eCollection 2022.
9
Region-Specific Characteristics of Astrocytes and Microglia: A Possible Involvement in Aging and Diseases.星形胶质细胞和小胶质细胞的区域特异性特征:可能与衰老和疾病有关。
Cells. 2022 Jun 12;11(12):1902. doi: 10.3390/cells11121902.
10
Autophagy in age-related macular degeneration.年龄相关性黄斑变性中的自噬作用。
Autophagy. 2023 Feb;19(2):388-400. doi: 10.1080/15548627.2022.2069437. Epub 2022 May 1.