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Science 27 July 2007:
Vol. 317. no. 5837, pp. 530 - 533
DOI: 10.1126/science.1142365

Reports

Rapid Synthesis and Synaptic Insertion of GluR2 for mGluR-LTD in the Ventral Tegmental Area

Manuel Mameli,1 Bénédicte Balland,1 Rafael Luján,2 Christian Lüscher1,3*

The activation of metabotropic glutamate receptors (mGluRs) leads to long-term depression (mGluR-LTD) at many synapses of the brain. The induction of mGluR-LTD is well characterized, whereas the mechanisms underlying its expression remain largely elusive. mGluR-LTD in the ventral tegmental area (VTA) efficiently reverses cocaine-induced strengthening of excitatory inputs onto dopamine neurons. We show that mGluR-LTD is expressed by an exchange of GluR2-lacking AMPA receptors for GluR2-containing receptors with a lower single-channel conductance. The synaptic insertion of GluR2 depends on de novo protein synthesis via rapid messenger RNA translation of GluR2. Regulated synthesis of GluR2 in the VTA is therefore required to reverse cocaine-induced synaptic plasticity.

1 Department of Basic Neuroscience, Medical Faculty, University of Geneva, CH-1211 Geneva, Switzerland.
2 Department Ciencias Médicas, Facultad de Medicina–Centro Regional de Investigaciones Biomedicas, Universidad de Castilla–La Mancha, 02006 Albacete, Spain.
3 Clinic of Neurology, Department of Clinical Neuroscience, Geneva University Hospital, CH-1211 Geneva, Switzerland.

* To whom correspondence should be addressed. E-mail: Christian.Luscher{at}medecine.unige.ch

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Recruitment of Calcium-Permeable AMPA Receptors during Synaptic Potentiation Is Regulated by CaM-Kinase I.
E. S. Guire, M. C. Oh, T. R. Soderling, and V. A. Derkach (2008)
J. Neurosci. 28, 6000-6009
   Abstract »    Full Text »    PDF »
Homer Interactions Are Necessary for Metabotropic Glutamate Receptor-Induced Long-Term Depression and Translational Activation.
J. A. Ronesi and K. M. Huber (2008)
J. Neurosci. 28, 543-547
   Abstract »    Full Text »    PDF »



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Science. ISSN 0036-8075 (print), 1095-9203 (online)