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本文引用的文献

1
Linking LRP12 CGG repeat expansion to inherited peripheral neuropathy.将LRP12基因CGG重复序列扩增与遗传性周围神经病联系起来。
J Neurol Neurosurg Psychiatry. 2025 Jan 16;96(2):140-149. doi: 10.1136/jnnp-2024-333403.
2
Autophagy preferentially degrades non-fibrillar polyQ aggregates.自噬优先降解无纤维状聚谷氨酰胺聚集体。
Mol Cell. 2024 May 16;84(10):1980-1994.e8. doi: 10.1016/j.molcel.2024.04.018.
3
The MuSK agonist antibody protects the neuromuscular junction and extends the lifespan in C9orf72-ALS mice.MuSK 激动剂抗体可保护神经肌肉接头并延长 C9orf72-ALS 小鼠的寿命。
Mol Ther. 2024 Jul 3;32(7):2176-2189. doi: 10.1016/j.ymthe.2024.05.016. Epub 2024 May 11.
4
Reactive astrocytes secrete the chaperone HSPB1 to mediate neuroprotection.反应性星形胶质细胞分泌伴侣蛋白 HSPB1 以介导神经保护作用。
Sci Adv. 2024 Mar 22;10(12):eadk9884. doi: 10.1126/sciadv.adk9884. Epub 2024 Mar 20.
5
Mitochondrial dysfunction and neurological disorders: A narrative review and treatment overview.线粒体功能障碍与神经疾病:综述与治疗概述
Life Sci. 2023 Dec 1;334:122257. doi: 10.1016/j.lfs.2023.122257. Epub 2023 Nov 8.
6
Lipid droplets modulate proteostasis, SQST-1/SQSTM1 dynamics, and lifespan in .脂滴调节蛋白质稳态、SQST-1/SQSTM1动态变化以及线虫的寿命。
iScience. 2023 Sep 16;26(10):107960. doi: 10.1016/j.isci.2023.107960. eCollection 2023 Oct 20.
7
Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease.神经传导研究在NOTCH2NLC相关神经元核内包涵体病中的诊断价值
J Peripher Nerv Syst. 2023 Dec;28(4):629-641. doi: 10.1111/jns.12599. Epub 2023 Oct 3.
8
Expression of expanded GGC repeats within NOTCH2NLC causes cardiac dysfunction in mouse models.NOTCH2NLC基因内扩展的GGC重复序列的表达在小鼠模型中导致心脏功能障碍。
Cell Biosci. 2023 Aug 29;13(1):157. doi: 10.1186/s13578-023-01111-6.
9
GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation.GGC 重复扩展导致 NOTCH2NLC 核糖体生物发生和翻译功能障碍。
Brain. 2023 Aug 1;146(8):3373-3391. doi: 10.1093/brain/awad058.
10
Expression of expanded GGC repeats within causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease.内源性扩展 GGC 重复序列的表达导致神经元核内包涵体病小鼠模型的行为缺陷和神经退行性变。
Sci Adv. 2022 Nov 25;8(47):eadd6391. doi: 10.1126/sciadv.add6391. Epub 2022 Nov 23.

热休克伴侣蛋白HSPB1通过恢复自噬通量减轻多聚甘氨酸诱导的神经变性。

Heat-shock chaperone HSPB1 mitigates poly-glycine-induced neurodegeneration via restoration of autophagic flux.

作者信息

Ding Ning, Song Yijie, Zhang Yuhang, Yu Wei, Li Xinnan, Li Wei, Li Lei

机构信息

School of Life Science and Technology, ShanghaiTech University, Shanghai, China.

Lingang Laboratory, Shanghai, China.

出版信息

Autophagy. 2025 Jun;21(6):1298-1315. doi: 10.1080/15548627.2025.2466144. Epub 2025 Feb 25.

DOI:10.1080/15548627.2025.2466144
PMID:39936620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12087658/
Abstract

The CGG repeat expansions in the 5'-UTR regions of certain genes have been implicated in various neurodegenerative and muscular disorders. However, the underlying pathogenic mechanisms are not well understood. In this study, we explore the role of the small molecular chaperone HSPB1 in counteracting neurodegeneration induced by poly-glycine (poly-G) aggregates. Employing a reporter system, we demonstrate that CGG repeat expansions within the 5'-UTR of the gene produce poly-G proteins, by repeat-associated non-AUG (RAN) translation. Through proximity labeling and subsequent mass spectrometry analysis, we characterize the composition of poly-G insoluble aggregates and reveal that these aggregates sequester key macroautophagy/autophagy receptors, SQSTM1/p62 and TOLLIP. This sequestration disrupts MAP1LC3/LC3 recruitment and impairs autophagosome formation, thereby compromising the autophagic pathway. Importantly, we show that HSPB1 facilitates the dissociation of these receptors from poly-G aggregates and consequently restores autophagic function. Overexpressing HSPB1 alleviates poly-G-induced neurodegeneration in mouse models. Taken together, these findings highlight a mechanistic basis for the neuroprotective effects of HSPB1 and suggest its potential as a therapeutic target in treating poly-G-associated neurodegenerative diseases.: AD: Alzheimer disease; AIF1/Iba1: allograft inflammatory factor 1; Baf A: bafilomycin A; BFP: blue fluorescent protein; CQ: chloroquine; EIF2A/eIF-2α: eukaryotic translation initiation factor 2A; FRAP: fluorescence recovery after photobleaching; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GFAP: glial fibrillary acidic protein; GFP: green fluorescent protein; HSPB1: heat shock protein family B (small) member 1; MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; NOTCH2NLC: notch 2 N-terminal like C; PD: Parkinson disease; PFA: paraformaldehyde; poly-A: poly-alanine; poly-G: poly-glycine; poly-R: poly-arginine; RAN translation: repeat-associated non-AUG translation; RBFOX3/NeuN: RNA binding fox-1 homolog 3; STED: stimulated emission depletion; TARDBP/TDP-43: TAR DNA binding protein; TG: thapsigargin; TOLLIP: toll interacting protein.

摘要

某些基因5'-UTR区域的CGG重复扩增与多种神经退行性疾病和肌肉疾病有关。然而,其潜在的致病机制尚不清楚。在本研究中,我们探讨了小分子伴侣HSPB1在对抗聚甘氨酸(poly-G)聚集体诱导的神经退行性变中的作用。利用报告系统,我们证明该基因5'-UTR内的CGG重复扩增通过重复相关非AUG(RAN)翻译产生poly-G蛋白。通过邻近标记和随后的质谱分析,我们对poly-G不溶性聚集体的组成进行了表征,并揭示这些聚集体隔离了关键的巨自噬/自噬受体SQSTM1/p62和TOLLIP。这种隔离破坏了MAP1LC3/LC3的募集并损害自噬体形成,从而损害自噬途径。重要的是,我们表明HSPB1促进这些受体从poly-G聚集体中解离,从而恢复自噬功能。在小鼠模型中过表达HSPB1可减轻poly-G诱导的神经退行性变。综上所述,这些发现突出了HSPB1神经保护作用的机制基础,并表明其作为治疗poly-G相关神经退行性疾病的治疗靶点的潜力。:AD:阿尔茨海默病;AIF1/Iba1:同种异体移植炎症因子1;Baf A:巴佛洛霉素A;BFP:蓝色荧光蛋白;CQ:氯喹;EIF2A/eIF-2α:真核翻译起始因子2A;FRAP:光漂白后荧光恢复;GAPDH:甘油醛-3-磷酸脱氢酶;GFAP:胶质纤维酸性蛋白;GFP:绿色荧光蛋白;HSPB1:热休克蛋白家族B(小)成员1;MAP1LC3B/LC3B:微管相关蛋白1轻链3β;NOTCH2NLC:Notch 2 N端样C;PD:帕金森病;PFA:多聚甲醛;poly-A:聚丙氨酸;poly-G:聚甘氨酸;poly-R:聚精氨酸;RAN翻译:重复相关非AUG翻译;RBFOX3/NeuN:RNA结合fox-1同源物3;STED:受激发射损耗;TARDBP/TDP-43:TAR DNA结合蛋白;TG:毒胡萝卜素;TOLLIP:Toll相互作用蛋白