Alterations in lysosomal and proteasomal markers in Parkinson's disease: Relationship to alpha-synuclein inclusions

• Published in: Neurobiology of disease Vol. 35; no. 3; pp. 385 - 398
• Main Authors: Chu, Yaping, Dodiya, Hemraj, Aebischer, Patrick, Olanow, C. Warren, Kordower, Jeffrey H
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.2009; Elsevier
• Subjects: Aged; Aged, 80 and over; Alpha-synuclein; alpha-Synuclein - genetics; alpha-Synuclein - metabolism; Animals; Cathepsin D - metabolism; Female; Genetic Vectors; HSC70 Heat-Shock Proteins - metabolism; Humans; Inclusion Bodies - metabolism; Inclusion Bodies - pathology; Lysosomal Membrane Proteins - metabolism; Lysosome; Male; Melanins - metabolism; Mutation; Neurology; Neurons - metabolism; Neurons - pathology; Parkinson Disease - metabolism; Parkinson Disease - pathology; Parkinson's disease; Proteasome; Proteasome Endopeptidase Complex - metabolism; Rats; Rats, Sprague-Dawley; Substantia Nigra - metabolism; Substantia Nigra - pathology; Parkinson's disease; Alpha-synuclein; Lysosome; Proteasome
• ISSN: 0969-9961; 1095-953X
• DOI: 10.1016/j.nbd.2009.05.023

Abstract We explored the relationship between ubiquitin proteasome system (UPS) and lysosomal markers and the formation of α-synuclein (α-syn) inclusions in nigral neurons in Parkinson disease (PD). Lysosome Associated Membrane Protein 1(LAMP1), Cathepsin D (CatD), and Heat Shock Protein73 (HSP73) immunoreactivity were significantly decreased within PD nigral neurons when compared to age-matched controls. This decrease was significantly greater in nigral neurons that contained α-syn inclusions. Immunoreactivity for 20S proteasome was similarly reduced in PD nigral neurons, but only in cells that contained inclusions. In aged control brains, there is staining for α-syn protein, but it is non-aggregated and there is no difference in LAMP1, CatD, HSP73 or 20S proteasome immunoreactivity between α-syn positive or negative neuromelanin-laden nigral neurons. Targeting over-expression of mutant human α-syn in the rat substantia nigra using viral vectors revealed that lysosomal and proteasomal markers were significantly decreased in the neurons that displayed α-syn-ir inclusions. These findings suggest that α-syn aggregation is a key feature associated with decline of proteasome and lysosome and support the hypothesis that cell degeneration in PD involves proteosomal and lysosomal dysfunction, impaired protein clearance, and protein accumulation and aggregation leading to cell death.