Pharmacological evidence for a metabotropic glutamate receptor heterodimer in neuronal cells

被引:66
作者
Delgado, David Moreno [1 ]
Moller, Thor C. [1 ]
Ster, Jeanne [1 ]
Giraldo, Jesus [2 ,3 ,4 ]
Maurel, Damien [1 ]
Rovira, Xavier [1 ]
Scholler, Pauline [1 ]
Zwier, Jurriaan M. [5 ]
Perroy, Julie [1 ]
Durroux, Thierry [1 ]
Trinquet, Eric [5 ]
Prezeau, Laurent [1 ]
Rondard, Philippe [1 ]
Pin, Jean-Philippe [1 ]
机构
[1] Univ Montpellier, INSERM, CNRS, IGF, Montpellier, France
[2] Univ Autonoma Barcelona, Inst Neurociencies, Lab Mol Neuropharmacol & Bioinformat, Bellaterra, Spain
[3] Univ Autonoma Barcelona, Unitat Bioestadist, Bellaterra, Spain
[4] Network Biomed Res Ctr Mental Hlth, Madrid, Spain
[5] CisBio Bioassays, Codolet, France
关键词
ALLOSTERIC MODULATORS; GPCR DIMERS; LOCALIZATION; ACTIVATION; REVEALS; MGLUR4; FRET; RAT; OLIGOMERIZATION; COOPERATIVITY;
D O I
10.7554/eLife.25233
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:33
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