Spautin-1 promotes PINK1-PRKN-dependent mitophagy and improves associative learning capability in an alzheimer disease animal model.

Juan Yi, He-Ling Wang, Guang Lu, Hailong Zhang, Lina Wang, Zhen-Yu Li, Liming Wang, Yihua Wu, Dajing Xia, Evandro F Fang, Han-Ming Shen
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Abstract

Spautin-1 is a well-known macroautophagy/autophagy inhibitor via suppressing the deubiquitinases USP10 and USP13 and promoting the degradation of the PIK3C3/VPS34-BECN1 complex, while its effect on selective autophagy remains poorly understood. Mitophagy is a selective form of autophagy for removal of damaged and superfluous mitochondria via the autophagy-lysosome pathway. Here, we report a surprising discovery that, while spautin-1 remains as an effective autophagy inhibitor, it promotes PINK1-PRKN-dependent mitophagy induced by mitochondrial damage agents. Mechanistically, spautin-1 facilitates the stabilization and activation of the full-length PINK1 at the outer mitochondrial membrane (OMM) via binding to components of the TOMM complex (TOMM70 and TOMM20), leading to the disruption of the mitochondrial import of PINK1 and prevention of PARL-mediated PINK1 cleavage. Moreover, spautin-1 induces neuronal mitophagy in Caenorhabditis elegans (C. elegans) in a PINK-1-PDR-1-dependent manner. Functionally, spautin-1 is capable of improving associative learning capability in an Alzheimer disease (AD) C. elegans model. In summary, we report a novel function of spautin-1 in promoting mitophagy via the PINK1-PRKN pathway. As deficiency of mitophagy is closely implicated in the pathogenesis of neurodegenerative disorders, the pro-mitophagy function of spautin-1 might suggest its therapeutic potential in neurodegenerative disorders such as AD.Abbreviations: AD, Alzheimer disease; ATG, autophagy related; BafA1, bafilomycin A1; CALCOCO2/NDP52, calcium binding and coiled-coil domain 2; CCCP, carbonyl cyanide m-chlorophenyl hydrazone; COX4/COX IV, cytochrome c oxidase subunit 4; EBSS, Earle's balanced salt; ECAR, extracellular acidification rate; GFP, green fluorescent protein; IA, isoamyl alcohol; IMM, inner mitochondrial membrane; MAP1LC3/LC3, microtubule associated protein 1 light chain 3; MMP, mitochondrial membrane potential; mtDNA, mitochondrial DNA; nDNA, nuclear DNA; O/A, oligomycin-antimycin; OCR, oxygen consumption rate; OMM, outer mitochondrial membrane; OPTN, optineurin; PARL, presenilin associated rhomboid like; PINK1, PTEN induced kinase 1; PRKN, parkin RBR E3 ubiquitin protein ligase; p-Ser65-Ub, phosphorylation of Ub at Ser65; TIMM23, translocase of inner mitochondrial membrane 23; TOMM, translocase of outer mitochondrial membrane; USP10, ubiquitin specific peptidase 10; USP13, ubiquitin specific peptidase 13; VAL, valinomycin; YFP, yellow fluorescent protein.

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Spautin-1能促进PINK1-PRKN依赖性有丝分裂,并提高阿尔茨海默病动物模型的联想学习能力。
Spautin-1 通过抑制去泛素化酶 USP10 和 USP13 以及促进 PIK3C3/VPS34-BECN1 复合物的降解,是一种众所周知的大自噬/自噬抑制剂,但其对选择性自噬的影响仍鲜为人知。线粒体吞噬是一种选择性自噬形式,通过自噬-溶酶体途径清除受损和多余的线粒体。在这里,我们报告了一个令人惊讶的发现,即尽管水飞蓟素-1 仍是一种有效的自噬抑制剂,但它能促进线粒体损伤剂诱导的 PINK1-PRKN 依赖性有丝分裂。从机理上讲,spautin-1 通过与 TOMM 复合物(TOMM70 和 TOMM20)的成分结合,促进了全长 PINK1 在线粒体外膜(OMM)的稳定和激活,从而破坏了 PINK1 的线粒体输入,阻止了 PARL 介导的 PINK1 裂解。此外,spautin-1 还能以 PINK-1-PDR-1 依赖性方式诱导秀丽隐杆线虫(C. elegans)神经细胞的有丝分裂。在功能上,Spautin-1能够改善阿尔茨海默病(AD)优雅子模型的联想学习能力。总之,我们报告了 spautin-1 通过 PINK1-PRKN 途径促进有丝分裂的新功能。由于有丝分裂的缺乏与神经退行性疾病的发病机制密切相关,所以斯鲍汀-1的促进有丝分裂功能可能表明它对神经退行性疾病(如AD)具有治疗潜力。
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