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Licensed Unlicensed Requires Authentication Published by De Gruyter June 17, 2011

LRRK2 Parkinson’s disease: from animal models to cellular mechanisms

  • Chin-Hsien Lin , Pei-I Tsai , Ruey-Meei Wu and Cheng-Ting Chien EMAIL logo


Mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) play a major role in the development of Parkinson’s disease. The most frequently defined mutations of LRRK2 are located in the central catalytic region of the LRRK2 protein, suggesting that dysregulations of its enzymatic activities contribute to PD pathogenesis. Herein, we review recent progress in research concerning how LRRK2 mutations affect cellular pathways and lead to neuronal degeneration. We also summarize recent evidence revealing the endogenous function of LRRK2 protein within cells. These concepts can be used to further understand disease pathophysiology and serve as a platform to develop therapeutic strategies for the treatment of Parkinson’s disease.

Corresponding author

Received: 2011-3-13
Accepted: 2011-4-19
Published Online: 2011-06-17
Published Online: 2011-06-17
Published in Print: 2011-08-01

©2011 by Walter de Gruyter Berlin Boston

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