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Formation of parkin aggregates and enhanced PINK1 accumulation during the pathogenesis of Parkinson's disease.

Authors
Um, JW; Park, HJ; Song, J; Jeon, I; Lee, G; Lee, PH; Chung, KC
Citation
Biochemical and biophysical research communications, 393(4):824-828, 2010
Journal Title
Biochemical and biophysical research communications
ISSN
0006-291X1090-2104
Abstract
Parkinson's disease (PD) is a devastating neurodegenerative disease characterized by a distinct set of motor symptoms. Loss-of-function mutations in PTEN-induced kinase 1 (PINK1) or parkin have been linked to early-onset autosomal recessive forms of familial PD. We have recently shown that parkin (an E3 ubiquitin ligase) and PINK1 (a serine/threonine kinase) affect one other's stability, solubility, and tendency to form cytoprotective aggresomes (Um et al., 2009). Here we validated the functional relevance of this mutual interaction under pathologic PD conditions, by investigating the changes of expression and solubility of these factors in response to PD-linked toxins. Consistent with our previous cell culture data, exposure of human dopaminergic neuroblastoma SH-SY5Y cells to PD-linked toxins (1-methyl-4-phenylpyridinium ion, 6-hydroxydopamine, or MG132) reduced Nonidet P-40-soluble parkin levels and induced PINK1 accumulation. Consistent with our previous findings from parkin knockout mice, rat models of PD (6-hydroxydopamine-, rotenone-, or MG132-induced PD) were also associated with an increase in soluble and insoluble PINK1 levels as well as enhanced formation of parkin aggregates. These findings suggest that both PINK1 and parkin play important roles in regulating the formation of Lewy bodies during the pathogenesis of sporadic and familial PD.
MeSH terms
1-Methyl-4-phenylpyridinium/toxicityAnimalsBrain/drug effects/*metabolism/pathologyCell LineDisease Models, AnimalHumansLeupeptins/toxicityLewy Bodies/*metabolism/pathologyMiceOxidopamine/toxicityParkinson Disease/*metabolism/pathologyProtein Kinases/*metabolismRatsSolubilityUbiquitin-Protein Ligases/*metabolism
DOI
10.1016/j.bbrc.2010.02.090
PMID
20171192
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Journal Papers > School of Medicine / Graduate School of Medicine > Physiology
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