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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基因中的突变与帕金森病(PD)的家族形式与Lewy病理相关联。 DNAJC13是一种与内体相关的蛋白质,并据信调节内体膜贩运。然而,DNAJC13突变和α-突触核蛋白(α-突触核蛋白(αsyn)病理到神经变性的机械链接仍然明显。在这项研究中,我们表明,PD连接的N855S-突变体DNAJC13导致内体隔室中的αSyn积累,可能是由于货物贩运早期内剂量有缺陷和/或再循环内体。在使用人αSyn转基因苍蝇的体内实验表明突变体DNAJC13不仅增加了飞纱中的不溶性αsyn的量,而且诱导了多巴胺能神经变性,粗眼表型和年龄依赖的运动障碍。这些研究结果表明,DNAJC13突变扰动多向内体贩运,导致αSyn的异常内体保留,这可能易于导致PD的神经变性过程。

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