Cell surface expression of 5-hydroxytryptamine type 3 receptors is promoted by RIC-3

Abstract

RIC-3 has been identified as a molecule essential for the recruitment of functional nicotinic acetylcholine receptors composed of α7, but it exhibits inhibitory effects on α4β2 or α3β4 receptors. In this study, we investigated the role of RIC-3 in the recruitment of 5-hydroxytryptamine type 3A (5-HT3A) receptors to the cell surface. Although RIC-3 is not essential for the surface transport of 5-HT3A receptors, we found that its presence enhances both receptor transport and function in a concentration-dependent manner. RIC-3 is localized to the endoplasmic reticulum, as evidenced by co-localization with the chaperone molecule, binding protein (BiP). RIC-3 is not detected at significant levels on the cell surface when expressed alone or in the presence of 5-HT3A. RIC-3 and 5-HT3A show a low level interaction that is transient (<4 h). That RIC-3 can interact with an endoplasmic reticulum-retained 5-HT3A construct, combined with the transient interaction observed and lack of significant surface-expressed RIC-3, suggests that RIC-3 may play a role in 5-HT3A receptor folding, assembly, or transport to the cell surface. © 2005 by The American Society for Biochemistry and Molecular Biology, Inc.