• 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

热休克蛋白在神经退行性变中的作用:潜在的治疗靶点

Impact of Heat Shock Proteins in Neurodegeneration: Possible Therapeutical Targets.

作者信息

Beretta Giangiacomo, Shala Aida Loshaj

机构信息

Department of Environmental Science and Policy, University of Milan, Milan, Italy.

Department of Pharmacy, Faculty of Medicine, University Hasan Prishtina, Pristina, Kosovo.

出版信息

Ann Neurosci. 2022 Jan;29(1):71-82. doi: 10.1177/09727531211070528. Epub 2022 Jan 31.

DOI:10.1177/09727531211070528
PMID:35875428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9305912/
Abstract

BACKGROUND

Human neurodegenerative diseases occur as a result of various factors. Regardless of the variety in the etiology of development, many of these diseases are characterized by the accumulation of pathological, misfolded proteins; hence, such diseases are considered as proteinopathies. While plenty of research study has been conducted in order to identify the pathophysiology of these proteinopathies, there is still a lack of understanding in terms of potential therapeutic targets.

SUMMARY

Molecular chaperones present the main workforce for cellular protection and stress response. Therefore, considering these functions, molecular chaperones present a promising target for research within the field of conformational diseases that arise from proteinopathies. Since the association between neurodegenerative disorders and their long-term consequences is well documented, the need for the development of new therapeutic strategies becomes even more critical.

KEY MESSAGE

In this review, we summarized the molecular function of heat shock proteins and recent progress on their role, involvement, and other mechanisms related to neurodegeneration caused by different etiological factors. Based on the relevant scientific data, we will highlight the functional classification of heat shock proteins, regulation, and their therapeutic potential for neurodegenerative disorders.

摘要

背景

人类神经退行性疾病由多种因素引发。尽管这些疾病的发病原因各不相同,但其中许多疾病的特征是病理性错误折叠蛋白的积累;因此,这类疾病被视为蛋白病。虽然为了确定这些蛋白病的病理生理学已经开展了大量研究,但在潜在治疗靶点方面仍缺乏了解。

总结

分子伴侣是细胞保护和应激反应的主要力量。因此,考虑到这些功能,分子伴侣是蛋白病引发的构象疾病领域中一个有前景的研究靶点。由于神经退行性疾病及其长期后果之间的关联已有充分记录,开发新治疗策略的需求变得更加迫切。

关键信息

在本综述中,我们总结了热休克蛋白的分子功能以及它们在由不同病因引起的神经退行性变中的作用、参与情况和其他相关机制的最新进展。基于相关科学数据,我们将重点介绍热休克蛋白的功能分类、调控及其对神经退行性疾病的治疗潜力。

相似文献

1
Impact of Heat Shock Proteins in Neurodegeneration: Possible Therapeutical Targets.热休克蛋白在神经退行性变中的作用:潜在的治疗靶点
Ann Neurosci. 2022 Jan;29(1):71-82. doi: 10.1177/09727531211070528. Epub 2022 Jan 31.
2
Neurodegeneration and the Heat Shock Protein 70 Machinery: Implications for Therapeutic Development.神经退行性变与热休克蛋白70机制:对治疗开发的启示
Curr Top Med Chem. 2016;16(25):2741-52. doi: 10.2174/1568026616666160413140741.
3
Folding or holding?-Hsp70 and Hsp90 chaperoning of misfolded proteins in neurodegenerative disease.折叠还是持留?——热休克蛋白 70 和 90 在神经退行性疾病中对错误折叠蛋白的伴侣作用。
J Biol Chem. 2022 May;298(5):101905. doi: 10.1016/j.jbc.2022.101905. Epub 2022 Apr 6.
4
Dealing with misfolded proteins: examining the neuroprotective role of molecular chaperones in neurodegeneration.应对错误折叠的蛋白质:研究分子伴侣在神经退行性变中的神经保护作用。
Molecules. 2010 Oct 8;15(10):6859-87. doi: 10.3390/molecules15106859.
5
Translational Shift of HSP90 as a Novel Therapeutic Target from Cancer to Neurodegenerative Disorders: An Emerging Trend in the Cure of Alzheimer's and Parkinson's Diseases.热休克蛋白90作为新型治疗靶点从癌症到神经退行性疾病的转化性转变:阿尔茨海默病和帕金森病治疗中的新趋势
Curr Drug Metab. 2017;18(9):868-876. doi: 10.2174/1389200218666170728115606.
6
Heat shock transcription factor 1-activating compounds suppress polyglutamine-induced neurodegeneration through induction of multiple molecular chaperones.热休克转录因子1激活化合物通过诱导多种分子伴侣来抑制多聚谷氨酰胺诱导的神经退行性变。
J Biol Chem. 2008 Sep 19;283(38):26188-97. doi: 10.1074/jbc.M710521200. Epub 2008 Jul 16.
7
Heat shock proteins at the crossroads between cancer and Alzheimer's disease.热休克蛋白处于癌症与阿尔茨海默病的交叉点上。
Biomed Res Int. 2014;2014:239164. doi: 10.1155/2014/239164. Epub 2014 Jul 24.
8
Mechanistic Insights into the Role of Molecular Chaperones in Protein Misfolding Diseases: From Molecular Recognition to Amyloid Disassembly.分子伴侣在蛋白质错误折叠疾病中的作用的机制见解:从分子识别到淀粉样纤维解体。
Int J Mol Sci. 2020 Dec 2;21(23):9186. doi: 10.3390/ijms21239186.
9
Stress and molecular chaperones in disease.疾病中的应激与分子伴侣
Int J Clin Lab Res. 2000;30(2):49-66. doi: 10.1007/s005990070016.
10
Heat shock protein 90 in neurodegenerative diseases.热休克蛋白 90 在神经退行性疾病中的作用。
Mol Neurodegener. 2010 Jun 3;5:24. doi: 10.1186/1750-1326-5-24.

引用本文的文献

1
Potential and value of rescuing dying neurons.拯救濒死神经元的潜力与价值
Neural Regen Res. 2026 Mar 1;21(3):1013-1022. doi: 10.4103/NRR.NRR-D-24-01134. Epub 2025 Apr 29.
2
HSP Modulators for the Correction of Cognitive, Mnemonic, and Behavioral Disorders After Prenatal Hypoxia.用于纠正产前缺氧后认知、记忆和行为障碍的热休克蛋白调节剂
Biomedicines. 2025 Apr 17;13(4):982. doi: 10.3390/biomedicines13040982.
3
Heat shock protein and Alzheimer's disease: an updated systematic review.热休克蛋白与阿尔茨海默病:一项最新的系统评价。

本文引用的文献

1
Heat shock protein is a key therapeutic target for nerve repair in autoimmune peripheral neuropathy and severe peripheral nerve injury.热休克蛋白是自身免疫性周围神经病和严重周围神经损伤神经修复的关键治疗靶点。
Brain Behav Immun. 2021 Jan;91:48-64. doi: 10.1016/j.bbi.2020.08.020. Epub 2020 Aug 25.
2
Small Heat Shock Proteins, Big Impact on Protein Aggregation in Neurodegenerative Disease.小分子热休克蛋白对神经退行性疾病中蛋白质聚集有重大影响。
Front Pharmacol. 2019 Sep 18;10:1047. doi: 10.3389/fphar.2019.01047. eCollection 2019.
3
Extracellular heat shock proteins in neurodegenerative diseases: New perspectives.
Ann Med Surg (Lond). 2025 Jan 7;87(3):1583-1588. doi: 10.1097/MS9.0000000000002887. eCollection 2025 Mar.
4
Chaperones as Potential Pharmacological Targets for Treating Protein Aggregation Illness.伴侣蛋白作为治疗蛋白质聚集疾病的潜在药理学靶点
Curr Protein Pept Sci. 2025 Jan 27. doi: 10.2174/0113892037338028241230092414.
5
Lateral hypothalamic area high-frequency deep brain stimulation rescues memory decline in aged rat: behavioral, molecular, and electrophysiological study.下丘脑外侧区高频深部脑刺激可挽救老年大鼠的记忆衰退:行为学、分子学及电生理学研究
Pflugers Arch. 2025 Mar;477(3):371-391. doi: 10.1007/s00424-024-03059-z. Epub 2025 Jan 21.
6
Different amyloid β42 preparations induce different cell death pathways in the model of SH-SY5Y neuroblastoma cells.不同的淀粉样蛋白 β42 制剂在 SH-SY5Y 神经母细胞瘤细胞模型中诱导不同的细胞死亡途径。
Cell Mol Biol Lett. 2024 Nov 17;29(1):143. doi: 10.1186/s11658-024-00657-8.
7
Protein arginine methyltransferases as regulators of cellular stress.蛋白质精氨酸甲基转移酶作为细胞应激的调节因子。
Exp Neurol. 2025 Feb;384:115060. doi: 10.1016/j.expneurol.2024.115060. Epub 2024 Nov 17.
8
Assessment of the therapeutic potential of Hsp70 activator against prion diseases using and models.使用[具体模型1]和[具体模型2]评估热休克蛋白70(Hsp70)激活剂对朊病毒疾病的治疗潜力。
Front Cell Dev Biol. 2024 Jul 22;12:1411529. doi: 10.3389/fcell.2024.1411529. eCollection 2024.
9
Senataxin deficiency disrupts proteostasis through nucleolar ncRNA-driven protein aggregation.Senataxin 缺陷通过核仁 ncRNA 驱动的蛋白质聚集破坏蛋白质稳态。
J Cell Biol. 2024 Jul 1;223(7). doi: 10.1083/jcb.202309036. Epub 2024 May 8.
10
Chaperones-A New Class of Potential Therapeutic Targets in Alzheimer's Disease.伴侣蛋白——阿尔茨海默病潜在治疗靶点的新类别。
Int J Mol Sci. 2024 Mar 17;25(6):3401. doi: 10.3390/ijms25063401.
细胞外热休克蛋白在神经退行性疾病中的作用:新视角。
Neurosci Lett. 2019 Oct 15;711:134462. doi: 10.1016/j.neulet.2019.134462. Epub 2019 Aug 30.
4
Up-regulation of heat shock protein 27 inhibits apoptosis in lumbosacral nerve root avulsion-induced neurons.热休克蛋白 27 的上调抑制腰骶神经根撕脱诱导的神经元凋亡。
Sci Rep. 2019 Aug 7;9(1):11468. doi: 10.1038/s41598-019-48003-9.
5
Global, regional, and national burden of neurological disorders, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.全球、区域和国家神经障碍负担,1990-2016 年:2016 年全球疾病负担研究的系统分析。
Lancet Neurol. 2019 May;18(5):459-480. doi: 10.1016/S1474-4422(18)30499-X. Epub 2019 Mar 14.
6
Local unfolding of the HSP27 monomer regulates chaperone activity.局部展开 HSP27 单体调节伴侣活性。
Nat Commun. 2019 Mar 6;10(1):1068. doi: 10.1038/s41467-019-08557-8.
7
Heat Shock Proteins in Alzheimer's Disease: Role and Targeting.阿尔茨海默病中的热休克蛋白:作用与靶向。
Int J Mol Sci. 2018 Sep 1;19(9):2603. doi: 10.3390/ijms19092603.
8
Phosphorylated recombinant HSP27 protects the brain and attenuates blood-brain barrier disruption following stroke in mice receiving intravenous tissue-plasminogen activator.磷酸化重组 HSP27 可保护大脑,并减轻接受静脉注射组织型纤溶酶原激活物的中风小鼠血脑屏障的破坏。
PLoS One. 2018 May 24;13(5):e0198039. doi: 10.1371/journal.pone.0198039. eCollection 2018.
9
Suppression of Alzheimer's disease-related phenotypes by the heat shock protein 70 inducer, geranylgeranylacetone, in APP/PS1 transgenic mice via the ERK/p38 MAPK signaling pathway.热休克蛋白70诱导剂香叶基香叶基丙酮通过ERK/p38 MAPK信号通路抑制APP/PS1转基因小鼠的阿尔茨海默病相关表型。
Exp Ther Med. 2017 Dec;14(6):5267-5274. doi: 10.3892/etm.2017.5253. Epub 2017 Oct 3.
10
Neurodegenerative disease: models, mechanisms, and a new hope.神经退行性疾病:模型、机制与新希望。
Dis Model Mech. 2017 May 1;10(5):499-502. doi: 10.1242/dmm.030205.