LRRK2 links genetic and sporadic Parkinson's disease.

LRRK2 links genetic and sporadic Parkinson's disease.
Biochem Soc Trans. 2019 Mar 05;:
Authors: Kluss JH, Mamais A, Cookson MR
Abstract
The past two decades in research has revealed the importance of leucine-rich repeat kinase 2 (LRRK2) in both monogenic and sporadic forms of Parkinson's disease (PD). In families, mutations in LRRK2 can cause PD with age-dependent but variable penetrance and genome-wide association studies have found variants of the gene that are risk factors for sporadic PD. Functional studies have suggested that the common mechanism that links all disease-associated variants is that they increase LRRK2 kinase activity, albeit in different ways. Here, we will discuss the roles of LRRK2 in areas of inflammation and vesicular trafficking in the context of monogenic and sporadic PD. We will also provide a hypothetical model that links inflammation and vesicular trafficking together in an effort to outline how these pathways might interact and eventually lead to neuronal cell death. We will also highlight the translational potential of LRRK2-specific kinase inhibitors for the treatment of PD.
PMID: 30837320 [PubMed - as supplied by publisher]

Source: Biochemical Society Transactions - March 4, 2019 Category: Biochemistry Authors: Kluss JH, Mamais A, Cookson MR Tags: Biochem Soc Trans Source Type: research