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LRRK2-RAB 轴在囊泡运输和 α-突触核蛋白传播中的调节作用。

The LRRK2-RAB axis in regulation of vesicle trafficking and α-synuclein propagation.

机构信息

Departments of Biomedical Sciences and Medicine and Neuroscience Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

Departments of Biomedical Sciences and Medicine and Neuroscience Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2020 Mar 1;1866(3):165632. doi: 10.1016/j.bbadis.2019.165632. Epub 2019 Dec 6.

Abstract

LRRK2 and SNCA, the gene for α-synuclein, are the two of the most important genetic factors of Parkinson's disease (PD). A-synuclein is aggregated and accumulated in neurons and glia in PD and considered the pathogenic culprit of the disease. A-synuclein aggregates spread from a few discrete regions of the brain to larger areas as the disease progresses through cell-to-cell propagation mechanism. LRRK2 is involved in the regulation of vesicle trafficking, in particular in the endolysosomal and autophagic pathways. Studies also suggest that LRRK2 might regulate the pathogenic actions of α-synuclein. However, the relationship between these two proteins in the pathogenesis of PD remains elusive. Here, we review the current literature on the pathophysiological function of LRRK2 with an emphasis on its role in the endolysosomal and autophagic pathways. We also propose a potential mechanism by which LRRK2 is involved in the regulation of aggregation and the propagation of α-synuclein.

摘要

LRRK2 和 SNCA,即α-突触核蛋白的基因,是帕金森病(PD)最重要的两个遗传因素。在 PD 中,α-突触核蛋白在神经元和神经胶质中聚集和积累,被认为是该疾病的致病元凶。随着疾病的进展,通过细胞间传播机制,α-突触核蛋白的聚集物从大脑的几个离散区域扩散到更大的区域。LRRK2 参与囊泡运输的调节,特别是在内溶酶体和自噬途径中。研究还表明,LRRK2 可能调节α-突触核蛋白的致病作用。然而,这两种蛋白质在 PD 发病机制中的关系仍不清楚。在这里,我们综述了 LRRK2 的生理病理学功能的现有文献,重点介绍了它在溶酶体和自噬途径中的作用。我们还提出了一个潜在的机制,即 LRRK2 参与调节α-突触核蛋白的聚集和传播。

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