Structural determinants of M2R involved in inhibition by Sigma-1R

Sigma-1 receptor (S1R) is a multimodal chaperone protein that is implicated in various pathophysiological conditions including drug addiction, Alzheimer's disease, and trophic lateral sclerosis (ALS). S1R interacts with various channels and receptors on the endoplasmic reticulum plasma membrane (PM). It has been reported that S1R alizes with the M2-muscarinic acetylcholine receptor (M2R) the soma of motoneurons, although a functional interaction between these two proteins has not been established. Here, investigated the regulation of M2R signaling by S1R electrophysiological recordings of GIRK currents in HEK293T cells. We observed that S1R strongly inhibited M2R-mediated activation of GIRK1/2, but the disease mutant linked to S1R E102Q, did not. The inhibitory effect of S1R was selective for M2R and wasn't seen when S1R was co-expressed other G i/o coupled receptors including M4R. Chimeric mutant receptors of M2R and M4R were generated analyzed, and this highlighted Ala401 in the transmembrane domain (TM6) of M2R and Glu172 as well as Glu175 extracellular loop 2 regions of M2R, as essential for the bition by S1R. Co-immunoprecipitation confirmed the physical interaction between M2R and S1R. Immunocytochemical beling of M2R and S1R expressed in HeLa cells, HEK293T and cultured hippocampal neurons, showed clear PM expression of M2R throughout the cell which was decreased coexpression with S1R but was still apparent. Taken together, our results show that S1R interacts with M2R to reduce both PM expression and function, and this involves TM6 and extracellular loop 2.