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dc.contributor.authorFonfria, E.
dc.contributor.authorMarshall, I.C.B.
dc.contributor.authorBoyfield, I.
dc.contributor.authorSkaper, S.D.
dc.contributor.authorHughes, J.P.
dc.contributor.authorOwen, D.
dc.contributor.authorZhang, W.
dc.contributor.authorMiller, B.A.
dc.contributor.authorBenham, C.D.
dc.contributor.authorMcNulty, S.
dc.date.accessioned2009-06-03T13:39:38Z
dc.date.available2009-06-03T13:39:38Z
dc.date.issued2005
dc.identifier.citationFonfria , E , Marshall , I C B , Boyfield , I , Skaper , S D , Hughes , J P , Owen , D , Zhang , W , Miller , B A , Benham , C D & McNulty , S 2005 , ' Amyloid β-peptide(1-42) and hydrogen peroxide-induced toxicity are mediated by TRPM2 in rat primary striatal cultures ' , Journal of Neurochemistry , vol. 95 , no. 3 , pp. 715-723 . https://doi.org/10.1111/j.1471-4159.2005.03396.x
dc.identifier.issn0022-3042
dc.identifier.otherPURE: 127899
dc.identifier.otherPURE UUID: d12c5f26-0e38-49e3-a6f7-f3f89a3548cf
dc.identifier.otherdspace: 2299/3484
dc.identifier.otherScopus: 27644507847
dc.identifier.urihttp://hdl.handle.net/2299/3484
dc.description‘The definitive version is available at www.blackwell-synergy.com '. Copyright by Blackwell Publishing. DOI: 10.1111/j.1471-4159.2005.03396.x [Full text of this article is not available in the UHRA]
dc.description.abstractAmyloid β-peptide (Aβ) is the main component of senile plaques which characterize Alzheimer's disease and may induce neuronal death through mechanisms which include oxidative stress. To date, the signalling pathways linking oxidant stress, a component of several neurodegenerative diseases, to cell death in the CNS are poorly understood. Melastatin-like transient receptor potential 2 (TRPM2) is a Ca2+-permeant non-selective cation channel, which responds to increases in oxidative stress levels in the cell and is activated by oxidants such as hydrogen peroxide. We demonstrate here that Aβ and hydrogen peroxide both induce death in cultured rat striatal cells which express TRPM2 endogenously. Transfection with a splice variant that acts as a dominant negative blocker of TRPM2 function (TRPM2-S) inhibited both hydrogen peroxide- and Aβ-induced increases in intracellular-free Ca2+ and cell death. Functional inhibition of TRPM2 activation by the poly(ADP-ribose)polymerase inhibitor SB-750139, a modulator of intracellular pathways activating TRPM2, attenuated hydrogen peroxide- and Aβ-induced cell death. Furthermore, a small interfering RNA which targets TRPM2, reduced TRPM2 mRNA levels and the toxicity induced by hydrogen peroxide and Aβ. These data demonstrate that activation of TRPM2, functionally expressed in primary cultures of rat striatum, contributes to Aβ- and oxidative stress-induced striatal cell death.en
dc.language.isoeng
dc.relation.ispartofJournal of Neurochemistry
dc.titleAmyloid β-peptide(1-42) and hydrogen peroxide-induced toxicity are mediated by TRPM2 in rat primary striatal culturesen
dc.contributor.institutionDepartment of Human and Environmental Sciences
dc.description.statusPeer reviewed
dcterms.dateAccepted2005
rioxxterms.versionofrecordhttps://doi.org/10.1111/j.1471-4159.2005.03396.x
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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