The Ca 2+ /Mn 2+ ion-pump PMR1 links elevation of cytosolic Ca 2+ levels to -synuclein toxicity in Parkinson's disease models

S. Büttner, L. Faes, W. N. Reichelt, F. Broeskamp, L. Habernig, S. Benke, N. Kourtis, D. Ruli, D. Carmona-Gutierrez, T. Eisenberg, P. D'Hooge, R. Ghillebert, V. Franssens, A. Harger, T. R. Pieber, P. Freudenberger, G. Kroemer, S. J. Sigrist, J. Winderickx, G. CallewaertN. Tavernarakis, F. Madeo

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    Résumé

    Parkinson's disease (PD) is characterized by the progressive loss of dopaminergic neurons, which arises from a yet elusive concurrence between genetic and environmental factors. The protein -synuclein (Syn), the principle toxic effector in PD, has been shown to interfere with neuronal Ca 2+ fluxes, arguing for an involvement of deregulated Ca 2+ homeostasis in this neuronal demise. Here, we identify the Golgi-resident Ca 2+ /Mn 2+ ATPase PMR1 (plasma membrane-related Ca 2+ -ATPase 1) as a phylogenetically conserved mediator of Syn-driven changes in Ca 2+ homeostasis and cytotoxicity. Expression of Syn in yeast resulted in elevated cytosolic Ca 2+ levels and increased cell death, both of which could be inhibited by deletion of PMR1. Accordingly, absence of PMR1 prevented Syn-induced loss of dopaminergic neurons in nematodes and flies. In addition, Syn failed to compromise locomotion and survival of flies when PMR1 was absent. In conclusion, the Syn-driven rise of cytosolic Ca 2+ levels is pivotal for its cytotoxicity and requires PMR1.

    langue originaleAnglais
    Pages (de - à)465-477
    Nombre de pages13
    journalCell Death and Differentiation
    Volume20
    Numéro de publication3
    Les DOIs
    étatPublié - 1 janv. 2013

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