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dc.contributor.authorRuiz de Martín Esteban, Samuel
dc.contributor.authorBenito Cuesta, Irene
dc.contributor.authorTerradillos Irastorza, Itziar ORCID
dc.contributor.authorMartínez Relimpio, Ana María
dc.contributor.authorArnanz, Andrea
dc.contributor.authorRuiz Pérez, Gonzalo
dc.contributor.authorKorn, Claudia
dc.contributor.authorRaposo, Catarina
dc.contributor.authorSarott, Roman C.
dc.contributor.authorWestphal, Matthias V.
dc.contributor.authorElezgarai Gabantxo, Izaskun ORCID
dc.contributor.authorCarreira, Erick M.
dc.contributor.authorHillard, Cecilia J.
dc.contributor.authorGrether, Uwe
dc.contributor.authorGrandes Moreno, Pedro Rolando ORCID
dc.contributor.authorGrande, María Teresa
dc.contributor.authorRomero, Julián
dc.date.accessioned2022-09-27T18:26:00Z
dc.date.available2022-09-27T18:26:00Z
dc.date.issued2022-04
dc.identifier.citationFrontiers in Pharmacology 13 : (2022) // Article ID 841766es_ES
dc.identifier.issn1663-9812
dc.identifier.urihttp://hdl.handle.net/10810/57850
dc.description.abstractThe distribution and roles of the cannabinoid CB2 receptor in the CNS are still a matter of debate. Recent data suggest that, in addition to its presence in microglial cells, the CB2 receptor may be also expressed at low levels, yet biologically relevant, in other cell types such as neurons. It is accepted that the expression of CB2 receptors in the CNS is low under physiological conditions and is significantly elevated in chronic neuroinflammatory states associated with neurodegenerative diseases such as Alzheimer's disease. By using a novel mouse model (CB2EGFP/f/f), we studied the distribution of cannabinoid CB2 receptors in the 5xFAD mouse model of Alzheimer's disease (by generating 5xFAD/CB2EGFP/f/f mice) and explored the roles of CB2 receptors in microglial function. We used a novel selective and brain penetrant CB2 receptor agonist (RO6866945) as well as mice lacking the CB2 receptor (5xFAD/CB2-/-) for these studies. We found that CB2 receptors are expressed in dystrophic neurite-associated microglia and that their modulation modifies the number and activity of microglial cells as well as the metabolism of the insoluble form of the amyloid peptide. These results support microglial CB2 receptors as potential targets for the development of amyloid-modulating therapies.es_ES
dc.description.sponsorshipFunding The present work has been supported by a grant from Ministerio de Ciencia e Innovacion (ref PID2019-108992RB-I00 and ref PID2019-107548RB-I00) to JR and PG, respectively, by the Basque Government (ref IT1230-19) to PG, and the Research and Education Component of the Advancing a Healthier Wisconsin Endowment at the Medical College of Wisconsin to CJH.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2019-108992RB-I00es_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2019-107548RB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectcannabinoidses_ES
dc.subjectCB2 receptores_ES
dc.subjectamyloides_ES
dc.subjectAlzheimer's diseasees_ES
dc.subjectmicrogliaes_ES
dc.titleCannabinoid CB2 Receptors Modulate Microglia Function and Amyloid Dynamics in a Mouse Model of Alzheimer's Diseasees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 Ruiz de Martín Esteban, Benito-Cuesta, Terradillos, Martínez- Relimpio, Arnanz, Ruiz-Pérez, Korn, Raposo, Sarott, Westphal, Elezgarai, Carreira, Hillard, Grether, Grandes, Grande and Romero. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fphar.2022.841766/fulles_ES
dc.identifier.doi10.3389/fphar.2022.841766
dc.departamentoesNeurocienciases_ES
dc.departamentoeuNeurozientziakes_ES


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© 2022 Ruiz de Martín Esteban, Benito-Cuesta, Terradillos, Martínez-
Relimpio, Arnanz, Ruiz-Pérez, Korn, Raposo, Sarott, Westphal, Elezgarai, Carreira,
Hillard, Grether, Grandes, Grande and Romero. This is an open-access article
distributed under the terms of the Creative Commons Attribution License (CC BY).
The use, distribution or reproduction in other forums is permitted, provided the original
author(s) and the copyright owner(s) are credited and that the original publication in
this journal is cited, in accordance with accepted academic practice. No use,
distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's license is described as © 2022 Ruiz de Martín Esteban, Benito-Cuesta, Terradillos, Martínez- Relimpio, Arnanz, Ruiz-Pérez, Korn, Raposo, Sarott, Westphal, Elezgarai, Carreira, Hillard, Grether, Grandes, Grande and Romero. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.