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Lipid rafts serve as signaling platforms for mGlu1 receptor-mediated calcium signaling in association with caveolin

BACKGROUND: Group I metabotropic glutamate receptors (mGlu1/5 receptors) have important roles in synaptic activity in the central nervous system. They modulate neuronal excitability by mobilizing intracellular Ca(2+) following receptor activation. Also, accumulating evidence has indicated the associ...

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Detalles Bibliográficos
Autores principales: Roh, Seung-Eon, Hong, Yun Hwa, Jang, Dong Cheol, Kim, Jun, Kim, Sang Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937055/
https://www.ncbi.nlm.nih.gov/pubmed/24512690
http://dx.doi.org/10.1186/1756-6606-7-9
Descripción
Sumario:BACKGROUND: Group I metabotropic glutamate receptors (mGlu1/5 receptors) have important roles in synaptic activity in the central nervous system. They modulate neuronal excitability by mobilizing intracellular Ca(2+) following receptor activation. Also, accumulating evidence has indicated the association of Ca(2+) signaling with lipid rafts. Caveolin, an adaptor protein found in a specialized subset of lipid rafts, has been reported to promote the localization of membrane proteins to lipid rafts. RESULTS: In the present study, we investigated the role of lipid rafts on the mGlu1α receptor-mediated Ca(2+) signaling in association with caveolin in hippocampal primary neurons and HEK293 cells. We show that the disruption of lipid rafts using methyl-β-cyclodextrin markedly decreased mGlu1α receptor-mediated Ca(2+) transients and lipid rafts localization of the receptor. Furthermore, transfection of mGlu1α receptor with mutated caveolin-binding domain reduced localization of the receptor to lipid rafts. Also, application of a peptide blocker of mGlu1α receptor and caveolin binding reduced the Ca(2+) signaling and the lipid rafts localization. CONCLUSIONS: Taken together, these results suggest that the binding of mGlu1α receptor to caveolin is crucial for its lipid rafts localization and mGlu1α receptor-mediated Ca(2+) transients.