Burst-dependent bidirectional plasticity in the cerebellum Is driven by presynaptic NMDA receptors

dc.contributor.authorBouvier, Guy
dc.contributor.authorHiggins, David
dc.contributor.authorSpolidoro, Maria
dc.contributor.authorCarrel, Damien
dc.contributor.authorMathieu, Benjamin
dc.contributor.authorLéna, Clément
dc.contributor.authorDieudonné, Stéphane
dc.contributor.authorBarbour, Boris
dc.contributor.authorBrunel, Nicolas
dc.contributor.authorCasado, Mariano
dc.date.accessioned2018-06-01T08:13:28Z
dc.date.available2018-06-01T08:13:28Z
dc.date.issued2016-03-24
dc.description.abstractNumerous studies have shown that cerebellar function is related to the plasticity at the synapses between parallel fibers and Purkinje cells. How specific input patterns determine plasticity outcomes, as well as the biophysics underlying plasticity of these synapses, remain unclear. Here, we characterize the patterns of activity that lead to postsynaptically expressed LTP using both in vivo and in vitro experiments. Similar to the requirements of LTD, we find that high-frequency bursts are necessary to trigger LTP and that this burst-dependent plasticity depends on presynaptic NMDA receptors and nitric oxide (NO) signaling. We provide direct evidence for calcium entry through presynaptic NMDA receptors in a subpopulation of parallel fiber varicosities. Finally, we develop and experimentally verify a mechanistic plasticity model based on NO and calcium signaling. The model reproduces plasticity outcomes from data and predicts the effect of arbitrary patterns of synaptic inputs on Purkinje cells, thereby providing a unified description of plasticity.en
dc.description.sponsorshipEC/FP7/238686/EU/Timing and plasticity in the olivo-cerebellar system/CEREBNETen
dc.identifier.issn2211-1247
dc.identifier.urihttps://depositonce.tu-berlin.de/handle/11303/7894
dc.identifier.urihttp://dx.doi.org/10.14279/depositonce-7055
dc.language.isoenen
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subject.ddc570 Biowissenschaften; Biologiede
dc.subject.ddc610 Medizin und Gesundheitde
dc.subject.othercerebellumen
dc.subject.othersynapsesen
dc.subject.otherparallel fibersen
dc.subject.otherPurkinje cellsen
dc.subject.otherNMDA receptorsen
dc.subject.otherpresynapticen
dc.subject.othernitric oxideen
dc.subject.otherLTPen
dc.titleBurst-dependent bidirectional plasticity in the cerebellum Is driven by presynaptic NMDA receptorsen
dc.typeArticleen
dc.type.versionpublishedVersionen
dcterms.bibliographicCitation.doi10.1016/j.celrep.2016.03.004en
dcterms.bibliographicCitation.issue1en
dcterms.bibliographicCitation.journaltitleCell Reportsen
dcterms.bibliographicCitation.originalpublishernameElsevieren
dcterms.bibliographicCitation.originalpublisherplaceNew York, NYen
dcterms.bibliographicCitation.pageend116en
dcterms.bibliographicCitation.pagestart104en
dcterms.bibliographicCitation.volume15en
tub.accessrights.dnbfreeen
tub.affiliationFak. 4 Elektrotechnik und Informatik::Inst. Softwaretechnik und Theoretische Informatik::FG Modellierung kognitiver Prozessede
tub.affiliation.facultyFak. 4 Elektrotechnik und Informatikde
tub.affiliation.groupFG Modellierung kognitiver Prozessede
tub.affiliation.instituteInst. Softwaretechnik und Theoretische Informatikde
tub.publisher.universityorinstitutionTechnische Universität Berlinen

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