Protein aggregation and degradation mechanisms in neurodegenerative diseases.

American journal of neurodegenerative disease Pub Date : 2013-01-01 Epub Date: 2013-03-08
Mari Takalo, Antero Salminen, Hilkka Soininen, Mikko Hiltunen, Annakaisa Haapasalo
{"title":"Protein aggregation and degradation mechanisms in neurodegenerative diseases.","authors":"Mari Takalo,&nbsp;Antero Salminen,&nbsp;Hilkka Soininen,&nbsp;Mikko Hiltunen,&nbsp;Annakaisa Haapasalo","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Neurodegenerative diseases are characterized by selective neuronal vulnerability and neurodegeneration in specific brain regions. The pathogenesis of these disorders centrally involves abnormal accumulation and aggregation of specific proteins, which are deposited in intracellular inclusions or extracellular aggregates that are characteristic for each disease. Increasing evidence suggests that genetic mutations or environmental factors can instigate protein misfolding and aggregation in these diseases. Consequently, neurodegenerative diseases are often considered as conformational diseases. This idea is further supported by studies implicating that impairment of the protein quality control (PQC) and clearance systems, such as the ubiquitin-proteasome system and autophagosome-lysosome pathway, may lead to the abnormal accumulation of disease-specific proteins. This suggests that similar pathological mechanisms may underlie the pathogenesis of the different neurodegenerative disorders. Interestingly, several proteins that are known to associate with neurodegenerative diseases have been identified as important regulators of PQC and clearance systems. In this review, we summarize the central features of abnormal protein accumulation in different common neurodegenerative diseases and discuss some aspects of specific disease-associated proteins regulating the PQC and clearance mechanisms, such as ubiquilin-1.</p>","PeriodicalId":72170,"journal":{"name":"American journal of neurodegenerative disease","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601466/pdf/ajnd0002-0001.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of neurodegenerative disease","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/3/8 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Neurodegenerative diseases are characterized by selective neuronal vulnerability and neurodegeneration in specific brain regions. The pathogenesis of these disorders centrally involves abnormal accumulation and aggregation of specific proteins, which are deposited in intracellular inclusions or extracellular aggregates that are characteristic for each disease. Increasing evidence suggests that genetic mutations or environmental factors can instigate protein misfolding and aggregation in these diseases. Consequently, neurodegenerative diseases are often considered as conformational diseases. This idea is further supported by studies implicating that impairment of the protein quality control (PQC) and clearance systems, such as the ubiquitin-proteasome system and autophagosome-lysosome pathway, may lead to the abnormal accumulation of disease-specific proteins. This suggests that similar pathological mechanisms may underlie the pathogenesis of the different neurodegenerative disorders. Interestingly, several proteins that are known to associate with neurodegenerative diseases have been identified as important regulators of PQC and clearance systems. In this review, we summarize the central features of abnormal protein accumulation in different common neurodegenerative diseases and discuss some aspects of specific disease-associated proteins regulating the PQC and clearance mechanisms, such as ubiquilin-1.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
神经退行性疾病中的蛋白质聚集和降解机制。
神经退行性疾病的特点是选择性神经元易感性和特定脑区域的神经变性。这些疾病的发病机制主要涉及特定蛋白质的异常积累和聚集,这些蛋白质沉积在细胞内包涵体或细胞外聚集体中,这是每种疾病的特征。越来越多的证据表明,基因突变或环境因素可引发这些疾病中的蛋白质错误折叠和聚集。因此,神经退行性疾病常被认为是构象性疾病。这一观点得到了进一步的支持,研究表明,蛋白质质量控制(PQC)和清除系统(如泛素-蛋白酶体系统和自噬体-溶酶体途径)的损伤可能导致疾病特异性蛋白质的异常积累。这表明类似的病理机制可能是不同神经退行性疾病发病机制的基础。有趣的是,一些已知与神经退行性疾病相关的蛋白质已被确定为PQC和清除系统的重要调节因子。在本文中,我们总结了不同常见神经退行性疾病中异常蛋白积累的主要特征,并讨论了调节PQC的特定疾病相关蛋白的一些方面及其清除机制,如泛素-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Exceptionally giant neglected sacral chordoma in a post-poliotic residual paralysis patient - a rare case scenario. Evaluation of willingness to obtain of Covid 19 vaccine in patients with multiple sclerosis. Short segment posterior fixation of unstable thoracolumbar vertebral fractures with fractured vertebra augmentation with intermediate pedicle screw - a clinicoradiological analysis. Single-cell RNA sequencing analysis and Alzheimer's disease: a bibliometric analysis. Leveraging genetic diversity to understand monogenic Parkinson's disease's landscape in AfrAbia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1