Abstract
Mutations in leucine-rich repeat kinase 2 (LRRK2) are thus far the most frequent genetic cause associated with autosomal dominant and idiopathic Parkinson's disease. To examine whether LRRK2 is directly associated with the pathological structures of Parkinson's disease, dementia with Lewy bodies, and other related disorders using highly specific antibodies to LRRK2. LRRK2 antibodies strongly labeled brainstem and cortical Lewy bodies, the pathological hallmarks of Parkinson's disease and dementia with Lewy bodies, respectively. We found that 20-100% (mean 60%) of alpha-synuclein-positive Lewy bodies contained LRRK2. While antibodies raised against various regions of LRRK2 were previously shown to label recombinant LRRK2 on Western blots, only antibodies raised against the N- and C-termini, but not the regions containing folded protein domains of LRRK2, immunolabeled Lewy bodies. In Alzheimer's disease, Hirano bodies were found to contain LRRK2 and the neurofibrillary tangles in progressive supranuclear palsy remained unlabeled. Information on the cellular localization of LRRK2 under normal and pathological conditions will deepen our understanding of its functions and molecular pathways relevant to the progression of Parkinson's disease and related disorders.
MeSH Terms
Adult
Aged
Aged, 80 and over
Brain Chemistry/physiology
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Middle Aged
Parkinson Disease/metabolism,pathology
Protein Serine-Threonine Kinases/analysis,metabolism
Tauopathies/metabolism,pathology
alpha-Synuclein/analysis,metabolism
tau Proteins/metabolism
Chemicals
alpha-Synuclein
tau Proteins
LRRK2 protein, human
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Protein Serine-Threonine Kinases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Perry George
Department of Pathology, Case Western Reserve University, Cleveland, Ohio, USA. george.perry@utsa.edu
Zhu Xiongwei
Babar Asim K
Siedlak Sandra L
Yang Qiwei
Ito Genta
Iwatsubo Takeshi
Smith Mark A
Chen Shu G
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