Protein Networks Associated with Native Metabotropic Glutamate 1 Receptors (mGlu(1)) in the Mouse Cerebellum

卷:12

Article

关键词: LONG-TERM POTENTIATION;    GABAERGIC SYNAPSES;    GABA(B) RECEPTORS;    PURKINJE-CELLS;    SYNAPTIC-TRANSMISSION;    VARIANTS MGLUR1A;    SPLICE VARIANTS;    NERVOUS-SYSTEM;    ACTIVATION;    CHANNELS;   

DOI  :  10.3390/cells12091325

来源: SCIE

【 摘 要 】

The metabotropic glutamate receptor 1 (mGlu(1)) plays a pivotal role in synaptic transmission and neuronal plasticity. Despite the fact that several interacting proteins involved in the mGlu(1) subcellular trafficking and intracellular transduction mechanisms have been identified, the protein network associated with this receptor in specific brain areas remains largely unknown. To identify novel mGlu(1)-associated protein complexes in the mouse cerebellum, we used an unbiased tissue-specific proteomic approach, namely co-immunoprecipitation followed by liquid chromatography/tandem mass spectrometry analysis. Many well-known protein complexes as well as novel interactors were identified, including G-proteins, Homer, d2 glutamate receptor, 14-3-3 proteins, and Na/K-ATPases. A novel putative interactor, KCTD12, was further investigated. Reverse co-immunoprecipitation with anti-KCTD12 antibodies revealed mGlu(1) in wild-type but not in KCTD12-knock-out homogenates. Freeze-fracture replica immunogold labeling co-localization experiments showed that KCTD12 and mGlu(1) are present in the same nanodomain in Purkinje cell spines, although at a distance that suggests that this interaction is mediated through interposed proteins. Consistently, mGlu(1) could not be co-immunoprecipitated with KCTD12 from a recombinant mammalian cell line co-expressing the two proteins. The possibility that this interaction was mediated via GABA(B) receptors was excluded by showing that mGlu(1) and KCTD12 still co-immunoprecipitated from GABA(B) receptor knock-out tissue. In conclusion, this study identifies tissue-specific mGlu(1)-associated protein clusters including KCTD12 at Purkinje cell synapses.