LRRK2 interactions with α-synuclein in Parkinson’s disease brains and in cell models View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2012-11-27

AUTHORS

Patrícia Silva Guerreiro, Yue Huang, Amanda Gysbers, Danni Cheng, Wei Ping Gai, Tiago Fleming Outeiro, Glenda Margaret Halliday

ABSTRACT

Mutations in the genes encoding leucine-rich repeat kinase 2 (LRRK2) and α-synuclein are associated with both autosomal dominant and idiopathic forms of Parkinson's disease (PD). α-Synuclein is the main protein in Lewy bodies, hallmark inclusions present in both sporadic and familial PD. We show that in PD brain tissue, the levels of LRRK2 are positively related to the increase in α-synuclein phosphorylation and aggregation in affected brain regions (amygdala and anterior cingulate cortex), but not in the unaffected visual cortex. In disease-affected regions, we show co-localization of these two proteins in neurons and Lewy body inclusions. Further, in vitro experiments show a molecular interaction between α-synuclein and LRRK2 under endogenous and over-expression conditions. In a cell culture model of α-synuclein inclusion formation, LRRK2 co-localizes with the α-synuclein inclusions, and knocking down LRRK2 increases the number of smaller inclusions. In addition to providing strong evidence for an interaction between LRRK2 and α-synuclein, our results shed light on the complex relationship between these two proteins in the brains of patients with PD and the underlying molecular mechanisms of the disease. More... »

PAGES

513-522

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00109-012-0984-y

DOI

http://dx.doi.org/10.1007/s00109-012-0984-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1026045143

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/23183827


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