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衰老及与年龄相关疾病中的小分子热休克蛋白

Small heat shock proteins in ageing and age-related diseases.

作者信息

Charmpilas Nikolaos, Kyriakakis Emmanouil, Tavernarakis Nektarios

机构信息

Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, 70013, Heraklion, Crete, Greece.

Department of Biology, University of Crete, 70013, Heraklion, Crete, Greece.

出版信息

Cell Stress Chaperones. 2017 Jul;22(4):481-492. doi: 10.1007/s12192-016-0761-x. Epub 2017 Jan 10.

DOI:10.1007/s12192-016-0761-x
PMID:28074336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5465026/
Abstract

Small heat shock proteins (sHSPs) are gatekeepers of cellular homeostasis across species, preserving proteome integrity under stressful conditions. Nonetheless, recent evidence suggests that sHSPs are more than molecular chaperones with merely auxiliary role. In contrast, sHSPs have emerged as central lifespan determinants, and their malfunction has been associated with the manifestation of neurological disorders, cardiovascular disease and cancer malignancies. In this review, we focus on the role of sHSPs in ageing and age-associated diseases and highlight the most prominent paradigms, where impairment of sHSP function has been implicated in human pathology.

摘要

小分子热休克蛋白(sHSPs)是跨物种细胞稳态的守护者,在应激条件下维持蛋白质组的完整性。尽管如此,最近的证据表明,sHSPs不仅仅是具有辅助作用的分子伴侣。相反,sHSPs已成为寿命的核心决定因素,其功能失调与神经疾病、心血管疾病和癌症恶性肿瘤的表现有关。在这篇综述中,我们聚焦于sHSPs在衰老和年龄相关疾病中的作用,并强调了最突出的范例,即sHSP功能受损与人类病理学有关。

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Small heat shock proteins in ageing and age-related diseases.衰老及与年龄相关疾病中的小分子热休克蛋白
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本文引用的文献

1
Small Heat-shock Proteins Prevent α-Synuclein Aggregation via Transient Interactions and Their Efficacy Is Affected by the Rate of Aggregation.小分子热休克蛋白通过瞬时相互作用防止α-突触核蛋白聚集,其功效受聚集速率影响。
J Biol Chem. 2016 Oct 21;291(43):22618-22629. doi: 10.1074/jbc.M116.739250. Epub 2016 Sep 1.
2
HSPB3 protein is expressed in motoneurons and induces their survival after lesion-induced degeneration.热休克蛋白 B3 蛋白在运动神经元中表达,并在损伤诱导的退化后诱导其存活。
Exp Neurol. 2016 Dec;286:40-49. doi: 10.1016/j.expneurol.2016.08.014. Epub 2016 Aug 24.
3
Extracellular Release and Signaling by Heat Shock Protein 27: Role in Modifying Vascular Inflammation.热休克蛋白27的细胞外释放与信号传导:在调节血管炎症中的作用
Front Immunol. 2016 Jul 26;7:285. doi: 10.3389/fimmu.2016.00285. eCollection 2016.
4
dFOXO Activates Large and Small Heat Shock Protein Genes in Response to Oxidative Stress to Maintain Proteostasis in Drosophila.dFOXO在果蝇中响应氧化应激激活大小热休克蛋白基因以维持蛋白质稳态。
J Biol Chem. 2016 Sep 2;291(36):19042-50. doi: 10.1074/jbc.M116.723049. Epub 2016 Jul 19.
5
HspB5/αB-crystallin increases dendritic complexity and protects the dendritic arbor during heat shock in cultured rat hippocampal neurons.热休克蛋白B5/αB-晶状体蛋白可增加培养的大鼠海马神经元树突复杂性,并在热休克期间保护树突分支。
Cell Mol Life Sci. 2016 Oct;73(19):3761-75. doi: 10.1007/s00018-016-2219-9. Epub 2016 Apr 16.
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Phosphorylated Heat Shock Protein 20 (HSPB6) Regulates Transforming Growth Factor-α-Induced Migration and Invasion of Hepatocellular Carcinoma Cells.磷酸化热休克蛋白20(HSPB6)调节转化生长因子-α诱导的肝癌细胞迁移和侵袭
PLoS One. 2016 Apr 5;11(4):e0151907. doi: 10.1371/journal.pone.0151907. eCollection 2016.
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Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases.热休克蛋白B8的转录诱导介导了导致运动神经元疾病的错误折叠蛋白的清除。
Sci Rep. 2016 Mar 10;6:22827. doi: 10.1038/srep22827.
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Changes in Drosophila mitochondrial proteins following chaperone-mediated lifespan extension confirm a role of Hsp22 in mitochondrial UPR and reveal a mitochondrial localization for cathepsin D.伴侣介导的寿命延长后果蝇线粒体蛋白的变化证实了Hsp22在线粒体未折叠蛋白反应中的作用,并揭示了组织蛋白酶D的线粒体定位。
Mech Ageing Dev. 2016 Apr;155:36-47. doi: 10.1016/j.mad.2016.02.011. Epub 2016 Feb 28.
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HSPB1 Inhibits the Endothelial-to-Mesenchymal Transition to Suppress Pulmonary Fibrosis and Lung Tumorigenesis.HSPB1 通过抑制血管内皮细胞向间充质细胞转化抑制肺纤维化和肺癌发生。
Cancer Res. 2016 Mar 1;76(5):1019-30. doi: 10.1158/0008-5472.CAN-15-0952. Epub 2016 Jan 7.
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Pharmacological chaperone for α-crystallin partially restores transparency in cataract models.α-晶状体蛋白的药理学伴侣分子可部分恢复白内障模型的透明度。
Science. 2015 Nov 6;350(6261):674-7. doi: 10.1126/science.aac9145.