mGluR1/TRPC3-mediated Synaptic Transmission and Calcium Signaling in Mammalian Central Neurons
Author(s) -
J. Hartmann,
Horst A. Henning,
Arthur Konnerth
Publication year - 2011
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a006726
Subject(s) - excitatory postsynaptic potential , biology , metabotropic glutamate receptor , postsynaptic potential , neuroscience , neurotransmission , synaptic plasticity , glutamatergic , trpc3 , metabotropic glutamate receptor 1 , post tetanic potentiation , inhibitory postsynaptic potential , long term depression , glutamate receptor , transient receptor potential channel , ampa receptor , receptor , biochemistry , trpc
Metabotropic glutamate receptors type 1 (mGluR1s) are required for a normal function of the mammalian brain. They are particularly important for synaptic signaling and plasticity in the cerebellum. Unlike ionotropic glutamate receptors that mediate rapid synaptic transmission, mGluR1s produce in cerebellar Purkinje cells a complex postsynaptic response consisting of two distinct signal components, namely a local dendritic calcium signal and a slow excitatory postsynaptic potential. The basic mechanisms underlying these synaptic responses were clarified in recent years. First, the work of several groups established that the dendritic calcium signal results from IP(3) receptor-mediated calcium release from internal stores. Second, it was recently found that mGluR1-mediated slow excitatory postsynaptic potentials are mediated by the transient receptor potential channel TRPC3. This surprising finding established TRPC3 as a novel postsynaptic channel for glutamatergic synaptic transmission.
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