MAPT/tau积累诱导的ISG15上调通过抑制HDAC6活性抑制自噬通量:阿尔茨海默病的恶性循环。

Qian Liu, Xin Wang, Zhi-Ting Fang, Jun-Ning Zhao, Xue-Xiang Rui, Bing-Ge Zhang, Ye He, Rui-Juan Liu, Jian Chen, Gao-Shang Chai, Gong-Ping Liu
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引用次数: 0

摘要

阿尔茨海默病(AD)是老年人普遍存在的一种神经退行性疾病,其特征是巨噬/自噬缺陷,导致细胞内MAPT/tau积累。虽然ISG15 (ISG15泛素样调节剂)已被确定为共济失调毛细血管扩张(a - t)中选择性自噬的调节因子,但其在AD中的作用仍未被探索。我们的研究表明,散发性AD患者和AD模型的大脑中ISG15水平在体内和体外升高。ISG15在细胞和海马中的过表达通过c端LRLRGG结合HDAC6抑制HDAC6(组蛋白去乙酰化酶6)活性。因此,这增加了CTTN(接触蛋白)乙酰化,破坏了CTTN和f -肌动蛋白向溶酶体的募集,并损害了自噬体(AP)-溶酶体(LY)的融合。这些破坏导致MAPT/tau积累、突触损伤、神经元丢失和认知缺陷。相反,在我们的HsMAPT(人类MAPT)病理模型中,ISG15敲低可以恢复HDAC6活性,促进AP-LY融合,改善认知功能。本研究确定ISG15是AD自噬通量的关键调节因子,提示靶向ISG15介导的自噬可能为AD提供治疗潜力。
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Upregulation of ISG15 induced by MAPT/tau accumulation represses autophagic flux by inhibiting HDAC6 activity: a vicious cycle in Alzheimer disease.

Alzheimer disease (AD), a prevalent neurodegenerative condition in the elderly, is marked by a deficit in macroautophagy/autophagy, leading to intracellular MAPT/tau accumulation. While ISG15 (ISG15 ubiquitin like modifier) has been identified as a regulator of selective autophagy in ataxia telangiectasia (A-T), its role in AD remains unexplored. Our study reveals elevated ISG15 levels in the brains of patients with sporadic AD and AD models in vivo and in vitro. ISG15 overexpression in cells and the hippocampus inhibited HDAC6 (histone deacetylase 6) activity through C-terminal LRLRGG binding to HDAC6. Consequently, this increased CTTN (cortactin) acetylation, disrupted CTTN and F-actin recruitment to lysosomes, and impaired autophagosome (AP)-lysosome (LY) fusion. These disruptions led to MAPT/tau accumulation, synaptic damage, neuronal loss, and cognitive deficits. Conversely, ISG15 knockdown in our HsMAPT (human MAPT) pathology model restored HDAC6 activity, promoted AP-LY fusion, and improved cognitive function. This study identifies ISG15 as a key regulator of autophagic flux in AD, suggesting that targeting ISG15-mediated autophagy could offer therapeutic potential for AD.Abbreviation: AAV: adeno-associated virus; AD: Alzheimer disease; ALP: autophagy-lysosomal pathway; ANOVA: analysis of variance; AP: autophagosome; BafA1: bafilomycin A1; CHX: cycloheximide; CQ: chloroquine; CTTN: cortactin; FC: fear conditioning; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GRIN/NMDARs: N-methyl-D-aspartate glutamate ionotropic receptor NMDA types; HDAC6: histone deacetylase 6; HEK293: human embryonic kidney 293; HsMAPT: human MAPT; IF: immunofluorescence; IHC: immunohistochemistry; IP: immunoprecipitation; ISG15: ISG15 ubiquitin like modifier; LAMP1: lysosomal associated membrane protein 1; LY: lysosome; MAPT: microtubule associated protein tau; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MWM: Morris water maze; NOR: novel object recognition; SQSTM1/p62: sequestosome 1; ZnF UBP: zinc finger ubiquitin-binding protein.

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