Fachbereich Veterinärmedizin


Service-Navigation

    Publikationsdatenbank

    Substitution p.A350V in Na(+)/Mg(2+) Exchanger SLC41A1, potentially associated with Parkinson's Disease, is a gain-of-function mutation (2013)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Kolisek, Martin (WE 2)
    Sponder, G. (WE 2)
    Mastrototaro, L. (WE 2)
    Smorodchenko, A.
    Launay, P.
    Vormann, J.
    Schweigel-Röntgen, M.
    Quelle
    PLoS one; 8(8) — S. e71096
    ISSN: 1932-6203
    Sprache
    Englisch
    Verweise
    URL (Volltext): http://edocs.fu-berlin.de/docs/receive/FUDOCS_document_000000019523
    DOI: 10.1371/journal.pone.0071096
    Pubmed: 23976986
    Kontakt
    Institut für Veterinär-Physiologie

    Oertzenweg 19 b
    14163 Berlin
    Tel.+49 30 838 62600 Fax.+49 30 838-62610
    email:physiologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Parkinson's disease (PD) is a complex multifactorial ailment predetermined by the interplay of various environmental and genetic factors. Systemic and intracellular magnesium (Mg) deficiency has long been suspected to contribute to the development and progress of PD and other neurodegenerative diseases. However, the molecular background is unknown. Interestingly, gene SLC41A1 located in the novel PD locus PARK16 has recently been identified as being a Na(+)/Mg(2+) exchanger (NME, Mg(2+) efflux system), a key component of cellular magnesium homeostasis. Here, we demonstrate that the substitution p.A350V potentially associated with PD is a gain-of-function mutation that enhances a core function of SLC41A1, namely Na(+)-dependent Mg(2+) efflux by 69±10% under our experimental conditions (10-minute incubation in high-Na(+) (145 mM) and completely Mg(2+)-free medium). The increased efflux capacity is accompanied by an insensitivity of mutant NME to cAMP stimulation suggesting disturbed hormonal regulation and leads to a reduced proliferation rate in p.A350V compared with wt cells. We hypothesize that enhanced Mg(2+)-efflux conducted by SLC41A1 variant p.A350V might result, in the long-term, in chronic intracellular Mg(2+)-deficiency, a condition that is found in various brain regions of PD patients and that exacerbates processes triggering neuronal damage.