Common anti-apoptotic roles of parkin and α-synuclein in human dopaminergic cells

Parkin. a product of the gene responsible for autosomal recessive juvenile parkinsonism, (AR-JP), is an important player in the pathogenic process of Parkinson's disease (PD). Despite numerous studies including search for the substrate of parkin as an E3 ubiquitin-protein ligase. the mechanism by which loss-of-function of parkin induces selective dopaminergic neuronal death remains unclear. Related to this issue. here we show that antisense knockdown of parkin causes apoptotic cell death of human dopaminergic SH-SY5Y cells associated with caspase activation and accompanied by accumulation of oxidative dopamine (DA) metabolites due to auto-oxidation of DOPA and DA. Forced expression of alpha-synuclein (alpha-SN), another familial PD gene product, prevented accumulation of oxidative DOPA/DA metabolites and cell death caused by parkin loss. Our findings indicate that both parkin and alpha-SN share a common pathway in DA metabolism whose abnormality leads to accumulation of oxidative DA metabolites and subsequent cell death. alpha 2005 Elsevier Inc. All rights reserved.