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

被引:25
作者
Bae, Eun-Jin [1 ,2 ,3 ]
Lee, Seung-Jae [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Biomed Sci, 103 Daehak Ro, Seoul 03080, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Med, Seoul 03080, South Korea
[3] Seoul Natl Univ, Coll Med, Neurosci Res Inst, Seoul 03080, South Korea
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2020年 / 1866卷 / 03期
基金
新加坡国家研究基金会;
关键词
Parkinson's disease; LRRK2; alpha-Synuclein; Vesicle trafficking; Protein aggregation; FAMILIAL PARKINSONS-DISEASE; GTPASE-ACTIVATING PROTEINS; RAB35; GTPASE; CELL-DEATH; LEWY BODY; KINASE; MUTATIONS; LOCALIZATION; AUTOPHAGY; GENE;
D O I
10.1016/j.bbadis.2019.165632
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
LRRK2 and SNCA, the gene for a-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 alpha-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 alpha-synuclein.
引用
收藏
页数:7
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