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N-Methyl-D-aspartate (NMDA) and cannabinoid CB receptors form functional complexes in cells of the central nervous system : insights into the therapeutic potential of neuronal and microglial NMDA receptors
Rivas Santisteban, Rafael (Universitat de Barcelona. Departament de Bioquímica i Biomedicina Molecular)
Lillo, Alejandro (Universitat de Barcelona. Departament de Bioquímica i Fisiologia)
Lillo Jové, Jaume (Universitat de Barcelona. Departament de Bioquímica i Biomedicina Molecular)
Rebassa, Joan Biel (Universitat de Barcelona. Departament de Bioquímica i Fisiologia)
Contestí, Joan S. (Universitat de Barcelona. Departament de Bioquímica i Fisiologia)
Saura Antolín, Carlos (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
Franco, Rafael (Universitat de Barcelona. Facultat de Química)
Navarro Rubio, Gemma (Universitat de Barcelona. Departament de Bioquímica i Fisiologia)

Date: 2021
Abstract: The cannabinoid CB receptor (CBR), which is a target to afford neuroprotection, and N-methyl-D-aspartate (NMDA) ionotropic glutamate receptors, which are key in mediating excitatory neurotransmission, are expressed in both neurons and glia. As NMDA receptors are the target of current medication in Alzheimer's disease patients and with the aim of finding neuromodulators of their actions that could provide benefits in dementia, we hypothesized that cannabinoids could modulate NMDA function. Immunocytochemistry was used to analyze the colocalization between CB and NMDA receptors; bioluminescence resonance energy transfer was used to detect CB-NMDA receptor complexes. Calcium and cAMP determination, mitogen-activated protein kinase (MAPK) pathway activation, and label-free assays were performed to characterize signaling in homologous and heterologous systems. Proximity ligation assays were used to quantify CB-NMDA heteromer expression in mouse primary cultures and in the brain of APP transgenic mice, an Alzheimer's disease model expressing the Indiana and Swedish mutated version of the human amyloid precursor protein (APP). In a heterologous system, we identified CB-NMDA complexes with a particular heteromer print consisting of impairment by cannabinoids of NMDA receptor function. The print was detected in activated primary microglia treated with lipopolysaccharide and interferon-γ. CBR activation blunted NMDA receptor-mediated signaling in primary hippocampal neurons from APP mice. Furthermore, imaging studies showed that in brain slices and in primary cells (microglia or neurons) from APP mice, there was a marked overexpression of macromolecular CB-NMDA receptor complexes thus becoming a tool to modulate excessive glutamate input by cannabinoids. The results indicate a negative cross-talk in CB-NMDA complexes signaling. The expression of the CB-NMDA receptor heteromers increases in both microglia and neurons from the APP transgenic mice, compared with levels in samples from age-matched control mice. The online version contains supplementary material available at 10. 1186/s13195-021-00920-6.
Grants: Agencia Estatal de Investigación SAF2017-84117-R
Ministerio de Economía, Industria y Competitividad PID2019-106615RB-100
Agencia Estatal de Investigación RTI2018-094204-B-I00
Note: This work was partially supported by the AARFD-17-503612 grant (to GN) from the US Alzheimer's Association
Rights: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Language: Anglès
Document: Article ; recerca ; Versió publicada
Subject: Alzheimer's disease ; Neuroprotection ; G-protein-coupled receptors ; Excitotoxicity
Published in: Alzheimer's research & therapy, Vol. 13 (november 2021) , ISSN 1758-9193

DOI: 10.1186/s13195-021-00920-6
PMID: 34749800


15 p, 3.2 MB

The record appears in these collections:
Articles > Research articles
Articles > Published articles

 Record created 2025-01-18, last modified 2025-12-22



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