Cannabinoid CB1 receptor gene inactivation in oligodendrocyte precursors disrupts oligodendrogenesis and myelination in mice

Cannabinoids are known to modulate oligodendrogenesis and developmental CNS myelination. However, the cell-autonomous action of these compounds on oligodendroglial cells in vivo, and the molecular mechanisms underlying these effects have not yet been studied. Here, by using oligodendroglial precurso...

Descripción completa

Detalles Bibliográficos
Autores: Sánchez De La Torre, Aníbal, Aguado Sánchez, Tania, Huerga-Gómez, Alba, Santamaría, Silvia, Gentile, Antonietta, Chara, Juan Carlos, Matute, Carlos, Monory, Krisztina, Mato, Susana, Guzmán Pastor, Manuel, Lutz, Beat, Galve Roperh, Ismael, Palazuelos Diego, Javier
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/88941
Acceso en línea:https://hdl.handle.net/20.500.14352/88941
Access Level:acceso abierto
Palabra clave:615.9
591.18
612.8
Cannabinoid CB1 receptor
Oligodendrogenesis
Myelination
Bioquímica (Biología)
Biología molecular (Biología)
Neurociencias (Biológicas)
2403 Bioquímica
2407 Biología Celular
2490 Neurociencias
Descripción
Sumario:Cannabinoids are known to modulate oligodendrogenesis and developmental CNS myelination. However, the cell-autonomous action of these compounds on oligodendroglial cells in vivo, and the molecular mechanisms underlying these effects have not yet been studied. Here, by using oligodendroglial precursor cell (OPC)-targeted genetic mouse models, we show that cannabinoid CB1 receptors exert an essential role in modulating OPC differentiation at the critical periods of postnatal myelination. We found that selective genetic inactivation of CB1 receptors in OPCs in vivo perturbs oligodendrogenesis and postnatal myelination by altering the RhoA/ROCK signaling pathway, leading to hypomyelination, and motor and cognitive alterations in young adult mice. Conversely, pharmacological CB1 receptor activation, by inducing E3 ubiquitin ligase-dependent RhoA proteasomal degradation, promotes oligodendrocyte development and CNS myelination in OPCs, an effect that was not evident in OPC-specific CB1 receptordeficient mice. Moreover, pharmacological inactivation of ROCK in vivo overcomes the defects in oligodendrogenesis and CNS myelination, and behavioral alterations found in OPC-specific CB1 receptor-deficient mice. Overall, this study supports a cellautonomous role for CB1 receptors in modulating oligodendrogenesis in vivo, which may have a profound impact on the scientific knowledge and therapeutic manipulation of CNS myelination by cannabinoids.