| Literature DB >> 28661401 |
David Moreno Delgado1, Thor C Møller1, Jeanne Ster1, Jesús Giraldo2,3, Damien Maurel1, Xavier Rovira1, Pauline Scholler1, Jurriaan M Zwier4, Julie Perroy1, Thierry Durroux1, Eric Trinquet4, Laurent Prezeau1, Philippe Rondard1, Jean-Philippe Pin1.
Abstract
Metabotropic glutamate receptors (mGluRs) are mandatory dimers playing important roles in regulating CNS function. Although assumed to form exclusive homodimers, 16 possible heterodimeric mGluRs have been proposed but their existence in native cells remains elusive. Here, we set up two assays to specifically identify the pharmacological properties of rat mGlu heterodimers composed of mGlu2 and 4 subunits. We used either a heterodimer-specific conformational LRET-based biosensor or a system that guarantees the cell surface targeting of the heterodimer only. We identified mGlu2-4 specific pharmacological fingerprints that were also observed in a neuronal cell line and in lateral perforant path terminals naturally expressing mGlu2 and mGlu4. These results bring strong evidence for the existence of mGlu2-4 heterodimers in native cells. In addition to reporting a general approach to characterize heterodimeric mGluRs, our study opens new avenues to understanding the pathophysiological roles of mGlu heterodimers.Entities:
Keywords: GPCR; cell biology; glutamate; heterodimer; mouse; neuroscience
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Year: 2017 PMID: 28661401 PMCID: PMC5540479 DOI: 10.7554/eLife.25233
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140