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dc.contributor.authorLYNCH, MARINAen
dc.contributor.authorLYNCH, MARINA ANNETTAen
dc.date.accessioned2014-10-21T15:45:47Z
dc.date.available2014-10-21T15:45:47Z
dc.date.issued2015en
dc.date.submitted2015en
dc.identifier.citationRaasay S. Jones and Marina A. Lynch, How dependent is synaptic plasticity on microglial phenotype?, Neuropharmacology, 96, A, 2015, 3 10en
dc.identifier.otherYen
dc.descriptionACCEPTEDen
dc.description.abstractMicroglia are particularly plastic cells which can be shifted from their resting state by numerous factors and adopt distinct phenotypes. The cells are multifunctional, though their main role is probably maintenance of homoeostasis. Resting cells are responsible for surveillance, whereas activation induces the cells to adopt neuroprotective or neurodetrimental roles, which are anti-inflammatory or pro-inflammatory respectively. The evidence indicates that activated cells with a pro-inflammatory phenotype predominate in neurodegenerative diseases and models of neurodegeneration and that this may significantly contribute to the deteriorating neuronal function. This question is considered in this review, in particular in the context of animal models of Alzheimer's disease (AD). This article is part of a Special Issue entitled ‘Neuroimmunology and Synaptic Function’en
dc.format.extent3 10en
dc.language.isoenen
dc.relation.ispartofseriesNeuropharmacologyen
dc.relation.ispartofseries96en
dc.relation.ispartofseriesAen
dc.rightsYen
dc.subjectNeuronal functionen
dc.subjectAlzheimer's disease;en
dc.subjectAgeen
dc.subjectInflammatory cytokinesen
dc.subjectAstrocytesen
dc.subjectMicrogliaen
dc.subjectNeuroinflammationen
dc.titleHow dependent is synaptic plasticity on microglial phenotype?en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/lynchmaen
dc.identifier.rssinternalid95928en
dc.identifier.doihttp://dx.doi.org/10.1016/j.neuropharm.2014.08.012en
dc.rights.ecaccessrightsopenAccess
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.identifier.urihttp://hdl.handle.net/2262/71681


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