Brain tyrosinase overexpression implicates age-dependent neuromelanin production in Parkinson's disease pathogenesis

Other authors

Institut Català de la Salut

[Carballo-Carbajal I, Laguna A, Romero-Giménez J, Cuadros T, Bové J, Martinez-Vicente M, Parent A, Gonzalez-Sepulveda M, Peñuelas N, Torra A, Rodríguez-Galván B] Grup de recerca en Malalties Neurodegeneratives, Vall d’Hebron Institut de Recerca, Barcelona, Spain. [Vila M] Grup de recerca en Malalties Neurodegeneratives, Vall d’Hebron Institut de Recerca, Barcelona, Spain. Department of Biochemistry and Molecular Biology, Autonomous University of Barcelona, Barcelona, Spain. Catalan Institution for Research and Advanced Studies (ICREA), Barcelona, Spain.

Vall d'Hebron Barcelona Hospital Campus

Publication date

2019-03-29T13:57:59Z

2019-03-29T13:57:59Z

2019-03-07



Abstract

Brain tyrosinase; Neuromelanin production; Parkinson’s


Tirosinasa cerebral; Producció de neuromelanina; Parkinson


Tirosinasa cerebral; Producción de neuromelanina; Parkinson


In Parkinson's disease (PD) there is a selective degeneration of neuromelanin-containing neurons, especially substantia nigra dopaminergic neurons. In humans, neuromelanin accumulates with age, the latter being the main risk factor for PD. The contribution of neuromelanin to PD pathogenesis remains unknown because, unlike humans, common laboratory animals lack neuromelanin. Synthesis of peripheral melanins is mediated by tyrosinase, an enzyme also present at low levels in the brain. Here we report that overexpression of human tyrosinase in rat substantia nigra results in age-dependent production of human-like neuromelanin within nigral dopaminergic neurons, up to levels reached in elderly humans. In these animals, intracellular neuromelanin accumulation above a specific threshold is associated to an age-dependent PD phenotype, including hypokinesia, Lewy body-like formation and nigrostriatal neurodegeneration. Enhancing lysosomal proteostasis reduces intracellular neuromelanin and prevents neurodegeneration in tyrosinase-overexpressing animals. Our results suggest that intracellular neuromelanin levels may set the threshold for the initiation of PD.

Document Type

Article


Published version

Language

English

Publisher

Nature Research

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Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

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