Calmodulin dependence of presynaptic metabotropic glutamate receptor signaling

被引:136
作者
O'Connor, V
El Far, O
Bofill-Cardona, E
Nanoff, C
Freissmuth, M
Karschin, A
Airas, JM
Betz, H
Boehm, S
机构
[1] Max Planck Inst Brain Res, Dept Neurochem, D-60528 Frankfurt, Germany
[2] Univ Vienna, Inst Pharmacol, A-1090 Vienna, Austria
[3] Max Planck Inst Biophys Chem, D-37070 Gottingen, Germany
关键词
D O I
10.1126/science.286.5442.1180
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glutamatergic neurotransmission is controlled by presynaptic metabotropic glutamate receptors (mGluRs). A subdomain in the intracellular carboxyl-terminal tail of group III mGluRs binds calmodulin and heterotrimeric guanosine triphosphate-binding protein (G protein) beta gamma subunits in a mutually exclusive manner. Mutations interfering with calmodulin binding and calmodulin antagonists inhibit G protein-mediated modulation of ionic currents by mGluR 7. Calmodulin antagonists also prevent inhibition of excitatory neurotransmission via presynaptic mGluRs. These results reveal a novel mechanism of presynaptic modulation in which Ca2+-calmodulin is required to release G protein beta gamma subunits from the C-tail of group III mGluRs in order to mediate glutamatergic autoinhibition.
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收藏
页码:1180 / 1184
页数:5
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