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The endocannabinoid 2-AG enhances spontaneous remyelination by targeting microglia

dc.contributor.authorMecha Rodríguez, Miriam
dc.contributor.authorYanguas Casás, Natalia
dc.contributor.authorFeliú Martínez, Ana
dc.contributor.authorMestre, L.
dc.contributor.authorCarrillo-Salinas, F.
dc.contributor.authorAzcoitia Elías, Iñigo
dc.contributor.authorYong, V. W.
dc.contributor.authorGuaza Rodríguez, Carmen
dc.date.accessioned2023-06-17T13:26:54Z
dc.date.available2023-06-17T13:26:54Z
dc.date.issued2019
dc.description.abstractRemyelination is an endogenous process by which functional recovery of damaged neurons is achieved by reinstating the myelin sheath around axons. Remyelination has been documented in multiple sclerosis (MS) lesions and experimental models, although it is often incomplete or fails to affect the integrity of the axon, thereby leading to progressive disability. Microglia play a crucial role in the clearance of the myelin debris produced by demyelination and in inflammation-dependent OPC activation, two processes necessary for remyelination to occur. We show here that following corpus callosum demyelination in the TMEV-IDD viral murine model of MS, there is spontaneous and partial remyelination that involves a temporal discordance between OPC mobilization and microglia activation. Pharmacological treatment with the endocannabinoid 2-AG enhances the clearance of myelin debris by microglia and OPC differentiation, resulting in complete remyelination and a thickening of the myelin sheath. These results highlight the importance of targeting microglia during the repair processes in order to enhance remyelination.
dc.description.departmentDepto. de Biología Celular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.sponsorshipRed Española de Esclerosis Múltiple (REEM)
dc.description.sponsorshipFondo de Investigación Sanitaria (FIS)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/56820
dc.identifier.doi10.1016/j.bbi.2018.12.013
dc.identifier.issn1090-2139
dc.identifier.officialurlhttps://www.sciencedirect.com/science/article/pii/S0889159118302411?via%3Dihub#!
dc.identifier.urihttps://hdl.handle.net/20.500.14352/13507
dc.journal.titleBrain, Behavior, and Immunity
dc.language.isoeng
dc.page.final126
dc.page.initial110
dc.publisherElsevier
dc.relation.projectID(SAF2013-42784-R); (SAF2016 76449-R)
dc.relation.projectID(RD12/0032/0008); (RD16/0015/0021)
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subject.cdu576
dc.subject.keywordRemyelination
dc.subject.keywordEndocannabinoids
dc.subject.keywordMicroglia
dc.subject.keywordPhagocytosis
dc.subject.keywordTMEV
dc.subject.ucmBiología celular (Biología)
dc.subject.unesco2407 Biología Celular
dc.titleThe endocannabinoid 2-AG enhances spontaneous remyelination by targeting microglia
dc.typejournal article
dc.volume.number77
dspace.entity.typePublication

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