Direct interaction and functional coupling between metabotropic glutamate receptor subtype 1 and voltage-sensitive Ca(v)2.1 Ca2+ channel

作者：Kitano J; Nishida M; Itsukaichi Y; Minami I; Ogawa M; Hirano T; Mori Y; Nakanishi S^*

来源：Journal of Biological Chemistry, 2003, 278(27): 25101-25108.

DOI：10.1074/jbc.M303266200

Intracellular Ca2+ concentrations ([Ca2+](i)) are regulated in a spatiotemporal manner via both entry of extracellular Ca2+ and mobilization of Ca2+ from intracellular stores. Metabotropic glutamate receptor subtype 1 (mGluR1) is a G protein-coupled receptor that stimulates the inositol 1,4,5-trisphosphate-Ca2+ signaling cascade, whereas Ca(v)2.1 is a pore-forming channel protein of P/Q-type voltage-sensitive Ca2+ channels. In this investigation, we showed that mGluR1 and Ca(v)2.1 are colocalized at dendrites of cerebellar Purkinje neurons and form the heteromeric assembly in both the brain and heterologously expressing COS-7 cells. This assembly occurs through the direct interaction between their carboxyl-terminal intracellular domains. Calcium imaging and whole-cell recording showed that mGluR1 inhibits Ca(v)2.1-mediated [Ca2+](i) increases and Ba2+ currents in HEK 293 cells expressing Ca(v)2.1 with auxiliary alpha2/delta and beta1 subunits, respectively. This inhibition occurred in a ligand-independent manner and was enhanced by pre-activation of mGluR1 in a ligand-dependent manner. In contrast, simultaneous stimulation of mGluR1 and Ca(v)2.1 induced large [Ca2+](i) increases. Furthermore, the temporally regulated inhibition and stimulation of [Ca2+](i) increases by mGluR1 and Ca(v)2.1 were observed at dendrites but not soma of cultured Purkinje neurons. These data suggest that the assembly of mGluR1 and Ca(v)2.1 provides the mechanism that ensures spatiotemporal regulation of [Ca2+](i) in glutamatergic neurotransmission.

• 出版日期2003-7-4