Show simple item record

dc.contributor.authorSaumell Esnaola, Miquel
dc.contributor.authorBarrondo Lacarra, Sergio ORCID
dc.contributor.authorGarcía del Caño, Gontzal
dc.contributor.authorGoicolea Altuna, María Aranzazu ORCID
dc.contributor.authorSallés Alvira, Joan
dc.contributor.authorLutz, Beat
dc.contributor.authorMonory, Krisztina
dc.date.accessioned2021-12-09T11:14:47Z
dc.date.available2021-12-09T11:14:47Z
dc.date.issued2021-11-16
dc.identifier.citationMolecules 26(22) : (2021) // Article ID 6897es_ES
dc.identifier.issn1420-3049,
dc.identifier.urihttp://hdl.handle.net/10810/54407
dc.description.abstractNumerous studies have investigated the roles of the type 1 cannabinoid receptor (CB1) in glutamatergic and GABAergic neurons. Here, we used the cell-type-specific CB1 rescue model in mice to gain insight into the organizational principles of plasma membrane targeting and Gαi/o protein signalling of the CB1 receptor at excitatory and inhibitory terminals of the frontal cortex and hippocampus. By applying biochemical fractionation techniques and Western blot analyses to synaptosomal membranes, we explored the subsynaptic distribution (pre-, post-, and extra-synaptic) and CB1 receptor compartmentalization into lipid and non-lipid raft plasma membrane microdomains and the signalling properties. These data infer that the plasma membrane partitioning of the CB1 receptor and its functional coupling to Gαi/o proteins are not biased towards the cell type of CB1 receptor rescue. The extent of the canonical Gαi/o protein-dependent CB1 receptor signalling correlated with the abundance of CB1 receptor in the respective cell type (glutamatergic versus GABAergic neurons) both in frontal cortical and hippocampal synaptosomes. In summary, our results provide an updated view of the functional coupling of the CB1 receptor to Gαi/o proteins at excitatory and inhibitory terminals and substantiate the utility of the CB1 rescue model in studying endocannabinoid physiology at the subcellular level.es_ES
dc.description.sponsorshipThis research was funded by the Basque Government (IT1230-19), MINECO, Spanish Ministry of Science, Innovation and Universities (CTQ2017-85686-R).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2017-85686-Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjecttype 1 cannabinoid receptor CB1es_ES
dc.subjectcholesteroles_ES
dc.subjecthippocampuses_ES
dc.subjectfrontal cortexes_ES
dc.subjectsynaptosomeses_ES
dc.subjectrescue modeles_ES
dc.subjectanti-CB1 antibodyes_ES
dc.titleSubsynaptic Distribution, Lipid Raft Targeting and G Protein-Dependent Signalling of the Type 1 Cannabinoid Receptor in Synaptosomes from the Mouse Hippocampus and Frontal Cortexes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2021-11-25T16:00:51Z
dc.rights.holder2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1420-3049/26/22/6897/htmes_ES
dc.identifier.doi10.3390/molecules26226897
dc.departamentoesFarmacología
dc.departamentoesNeurociencias
dc.departamentoesQuímica analítica
dc.departamentoeuFarmakologia
dc.departamentoeuNeurozientziak
dc.departamentoeuKimika analitikoa


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).