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dc.contributor.authorEsposito, Elga
dc.contributor.authorZhang, Fang
dc.contributor.authorPark, Ji-Hyun
dc.contributor.authorMandeville, Emiri T
dc.contributor.authorLi, Wenlu
dc.contributor.authorCuartero, María Isabel
dc.contributor.authorLizasoaín, Ignacio
dc.contributor.authorMoro, María A
dc.contributor.authorLo, Eng H
dc.date.accessioned2023-10-16T11:01:28Z
dc.date.available2023-10-16T11:01:28Z
dc.date.issued2022-12
dc.identifier.citationStroke. 2022 Dec;53(12):e507-e511.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16561
dc.description.abstractBACKGROUND The immune response to acute cerebral ischemia is a major factor in stroke pathobiology. Circadian biology modulates some aspects of immune response. The goal of this study is to compare key parameters of immune response during the active/awake phase versus inactive/sleep phase in a mouse model of transient focal cerebral ischemia. METHODS Mice were housed in normal or reversed light cycle rooms for 3 weeks, and then they were blindly subjected to transient focal cerebral ischemia. Flow cytometry was used to examine immune responses in blood, spleen, and brain at 3 days after ischemic onset. RESULTS In blood, there were higher levels of circulating T cells in mice subjected to focal ischemia during zeitgeber time (ZT)1-3 (inactive or sleep phase) versus ZT13-15 mice (active or awake phase). In the spleen, organ weight and immune cell numbers were lower in ZT1-3 versus ZT13-15 mice. Consistent with these results, there was an increased infiltration of activated T cells into brain at ZT1-3 compared with ZT13-15. CONCLUSIONS This proof-of-concept study indicates that there are significant diurnal effects on the immune response after focal cerebral ischemia in mice. Hence, therapeutic strategies focused on immune targets should be reassessed to account for the effects of diurnal rhythms and circadian biology in nocturnal rodent models of stroke.es_ES
dc.description.sponsorshipSupported in part by the Rappaport Foundation and Leducq Foundation. The authors thank all team members of the MGH animal facility for help with light schedule switching.es_ES
dc.language.isoenges_ES
dc.publisherLippincott Williams & Wilkins (LWW) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshBrain Ischemia es_ES
dc.subject.meshStroke es_ES
dc.subject.meshIschemic Attack, Transientes_ES
dc.subject.meshAnimals es_ES
dc.subject.meshMice es_ES
dc.subject.meshSpleen es_ES
dc.subject.meshMice, Inbred C57BL es_ES
dc.subject.meshBrain es_ES
dc.subject.meshCerebral Infarction es_ES
dc.subject.meshIschemia es_ES
dc.subject.meshImmunity es_ES
dc.titleDiurnal Differences in Immune Response in Brain, Blood and Spleen After Focal Cerebral Ischemia in Mice.es_ES
dc.typejournal articlees_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID36321457es_ES
dc.format.volume53es_ES
dc.format.number12es_ES
dc.format.pagee507es_ES
dc.identifier.doi10.1161/STROKEAHA.122.040547es_ES
dc.contributor.funderFondation Leducq es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1524-4628es_ES
dc.relation.publisherversion10.1161/STROKEAHA.122.040547es_ES
dc.identifier.journalStrokees_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Fisiopatología Neurovasculares_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsopen accesses_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 Internacional