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Parkin is known to mitigate α-synuclein–induced neuronal cell death in vitro, which suggests that the parkin gene therapy is a candidate for therapeutic strategies for Parkinson's disease (PD). In the present study, the parkin gene therapy was investigated for its ameliorative effects on α-synucleinopathy in substantia nigra (SN) of rats. A recombinant adeno-associated viral (rAAV) vector system has frequently been used for the gene transfer to rat SN, and we have previously demonstrated that this technique induced the α-synucleinopathy, which closely resembles pathogenetic changes in PD. Therefore, in the present study, the effect of parkin was examined by co-infection of rAAV-parkin with rAAV-α-synuclein into dopaminergic neurons in SN. At 13 weeks post-rAAV infection, α-synuclein overexpression induced dopaminergic neuron loss, while co-expression of parkin mitigated the α-synuclein toxicity. Moreover, α-synuclein–induced dopaminergic neuron loss consequently resulted in motor dysfunction, which was also mitigated by parkin. Taken together, our results indicate that the parkin gene therapy is effective against α-synucleinopathy, suggesting its potential suitability for patients with PD.