Regulation of Autophagy by LRRK2 in Caenorhabditis elegans

被引:15
作者
Saha, Shamol
Liu-Yesucevitz, Liqun
Wolozin, Benjamin [1 ,2 ]
机构
[1] Boston Univ, Sch Med, Dept Pharmacol, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
关键词
Autophagy; Parkinson's disease; Heat shock protein; Mitochondria; Endoplasmic reticulum; Stress; PROTEIN; DYSFUNCTION;
D O I
10.1159/000355654
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Mutations in LRRK2 (leucine-rich repeat kinase 2) are a common cause of familial Parkinson's disease. However, the mechanisms through which LRRK2 mutations contribute to neurodegeneration are poorly understood. Objective:We investigated the effects of WT, G2019S (GS), R1441C (RC) and kinase dead LRRK2 across multiple different cellular compartments in order to gain insight into the breadth of LRRK2 effects on cellular function. Methods: Nematodes expressing lgg-1::RFP, hsp1::GFP, hsp4::GFP and hsp6::GFP were crossed to nematode lines expressing WT, GS, RC or kinase dead LRRK2. Results: We observed that GS and RC LRRK2 inhibited autophagy, while WT, GS and RC LRRK2 increased the response of the mitochondrial hsp6 reporter to stress. The response of the hsp reporters under basal conditions was more nuanced. Conclusion: These results support a putative role of LRRK2 in the autophagic and mitochondrial systems. (C) 2013 S. Karger AG, Basel
引用
收藏
页码:110 / 113
页数:4
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