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首页> 外文期刊>Human Molecular Genetics >Parkinson’s disease-linked DNAJC13 mutation aggravates alpha-synuclein-induced neurotoxicity through perturbation of endosomal trafficking
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Parkinson’s disease-linked DNAJC13 mutation aggravates alpha-synuclein-induced neurotoxicity through perturbation of endosomal trafficking

机译:帕金森病联合的DNAJC13突变通过对内体贩运的扰动加剧了α-突触核蛋白诱导的神经毒性

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摘要

Mutations in DNAJC13 gene have been linked to familial form of Parkinson’s disease (PD) with Lewy pathology. DNAJC13 is an endosome-related protein and believed to regulate endosomal membrane trafficking. However, the mechanistic link between DNAJC13 mutation and α-synuclein (αSYN) pathology toward neurodegeneration remains poorly understood. In this study, we showed that PD-linked N855S-mutant DNAJC13 caused αSYN accumulation in the endosomal compartment, presumably due to defective cargo trafficking from the early endosome to the late and/or recycling endosome. In vivo experiments using human αSYN transgenic flies showed that mutant DNAJC13 not only increased the amount of insoluble αSYN in fly head but also induced dopaminergic neurodegeneration, rough eye phenotype and age-dependent locomotor impairment. Together, these findings suggest that DNAJC13 mutation perturbs multi-directional endosomal trafficking, resulting in the aberrant endosomal retention of αSYN, which might predispose to the neurodegenerative process that leads to PD.
机译:DNAJC13基因突变与家族性帕金森病(PD)的Lewy病理学有关。DNAJC13是一种内体相关蛋白,据信可调节内体膜运输。然而,DNAJC13突变和α-突触核蛋白(α-SYN)病理学与神经退行性变之间的机制联系仍知之甚少。在这项研究中,我们发现PD连接的N855S突变体DNAJC13导致α-SYN在内体室中积累,这可能是由于从早期内体到晚期和/或回收内体的货物运输缺陷所致。利用人α-SYN转基因果蝇进行的体内实验表明,突变体DNAJC13不仅增加了果蝇头部不溶性α-SYN的数量,而且还诱导多巴胺能神经退行性变、眼睛粗糙表型和年龄依赖性运动损伤。总之,这些发现表明DNAJC13突变扰乱了多向内体运输,导致α-SYN的异常内体保留,这可能会诱发导致PD的神经退行性过程。

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