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Cerebellar astrocytes co-express several ADP receptors. Presence of functional P2Y(13)-like receptors

Astrocytes exhibit a form of excitability based on variations of intracellular Ca(2+) concentration in response to various stimuli, including ADP, ATP, UTP and dinucleotides. Here, we investigate the presence of the recently cloned ADP-sensitive receptors, P2Y(12) and P2Y(13) subtypes, which are neg...

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Detalles Bibliográficos
Autores principales: Carrasquero, Luz María G., Delicado, Esmerilda G., Jiménez, Ana I., Pérez-Sen, Raquel, Miras-Portugal, M. Teresa
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096534/
https://www.ncbi.nlm.nih.gov/pubmed/18404500
http://dx.doi.org/10.1007/s11302-005-6211-3
Descripción
Sumario:Astrocytes exhibit a form of excitability based on variations of intracellular Ca(2+) concentration in response to various stimuli, including ADP, ATP, UTP and dinucleotides. Here, we investigate the presence of the recently cloned ADP-sensitive receptors, P2Y(12) and P2Y(13) subtypes, which are negatively coupled to adenylate cyclase, in cerebellar astrocytes. We checked the effect of specific agonists, 2-methylthioadenosine diphosphate (2MeSADP) and ADP, on adenylate cyclase stimulation induced by isoproterenol. Both agonists significantly reduced the cAMP accumulation induced by isoproterenol. The inhibitory effect was concentration-dependent with IC(50) values of 46 ± 13 and 23 ± 14 nM for 2MeSADP and ADP, respectively. The experiments were carried out in the presence of MRS-2179, a specific antagonist of P2Y(1) receptor, to avoid any contribution of this receptor. Using fura-2 microfluorimetry we also proved that astrocytes responded to 2MeSADP stimulations with calcium responses in the absence and also in the presence of MRS-2179. Both effects, inhibition of adenylate cyclase and intracellular calcium mobilization, were not modified by 2MeSAMP, an antagonist of P2Y(12) receptor, suggesting that were mediated by P2Y(13)-like receptors.