TY - JOUR
T1 - Homer-dependent cell surface expression of metabotropic glutamate receptor type 5 in neurons
AU - Ango, Fabrice
AU - Robbe, David
AU - Tu, Jian Cheng
AU - Xiao, Bo
AU - Worley, Paul F.
AU - Pin, Jean Philippe
AU - Bockaert, Joël
AU - Fagni, Laurent
N1 - Funding Information:
F.A. is a grant holder of Sanofi-Synthélabo, Biologie Moléculaire (Strasbourg, France). This work was supported by grants from Fon-dation pour la Recherche Médicale, Bayer (France), INSERM, CNRS, Association Franc¸aise contre les Myopathies.
PY - 2002
Y1 - 2002
N2 - The metabotropic glutamate (mGlu) receptors are a family of receptors involved in the tuning of fast excitatory synaptic transmission in the brain. Experiments performed in heterologous expression systems suggest that cell surface expression of group I mGlu receptors is controlled by their auxiliary protein, Homer. However, whether or not this also applies to neurons remains controversial. Here we show that in cultured cerebellar granule cells, the group I mGlu receptor subtype, mGlu5, transfected alone is functionally expressed at the surface of these neurons. Transfected Homer1b caused intracellular retention and clustering of this receptor at synaptic sites. Recombinant Homer1a alone did not affect cell surface expression of the receptor, but in neurons transfected with Homer1b, excitation-induced expression of native Homer1a reversed the intracellular retention of mGlu5 receptors, resulting in the receptor trafficking to synaptic membranes. Transfected Homer1a also increased the latency and amplitude of the mGlu5 receptor Ca2+ response. These results indicate that Homer1 proteins regulate synaptic cycling and Ca2+ signaling of mGlu5 receptors, in response to neuronal activity.
AB - The metabotropic glutamate (mGlu) receptors are a family of receptors involved in the tuning of fast excitatory synaptic transmission in the brain. Experiments performed in heterologous expression systems suggest that cell surface expression of group I mGlu receptors is controlled by their auxiliary protein, Homer. However, whether or not this also applies to neurons remains controversial. Here we show that in cultured cerebellar granule cells, the group I mGlu receptor subtype, mGlu5, transfected alone is functionally expressed at the surface of these neurons. Transfected Homer1b caused intracellular retention and clustering of this receptor at synaptic sites. Recombinant Homer1a alone did not affect cell surface expression of the receptor, but in neurons transfected with Homer1b, excitation-induced expression of native Homer1a reversed the intracellular retention of mGlu5 receptors, resulting in the receptor trafficking to synaptic membranes. Transfected Homer1a also increased the latency and amplitude of the mGlu5 receptor Ca2+ response. These results indicate that Homer1 proteins regulate synaptic cycling and Ca2+ signaling of mGlu5 receptors, in response to neuronal activity.
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U2 - 10.1006/mcne.2002.1100
DO - 10.1006/mcne.2002.1100
M3 - Article
C2 - 12093163
AN - SCOPUS:0036311506
SN - 1044-7431
VL - 20
SP - 323
EP - 329
JO - Molecular and Cellular Neuroscience
JF - Molecular and Cellular Neuroscience
IS - 2
ER -