Calcium-Sensing Receptor Internalization Is β -Arrestin-Dependent and Modulated by Allosteric Ligands

• Published in: Molecular pharmacology Vol. 96; no. 4; pp. 463 - 474
• Main Authors: Mos, Iris, Jacobsen, Stine E, Foster, Simon R, Bräuner-Osborne, Hans
• Format: Journal Article
• Language: English
• Published: United States 01.10.2019
• Subjects: Allosteric Regulation; beta-Arrestins - metabolism; Calcium - blood; Fluorescence Resonance Energy Transfer; Gene Knockout Techniques; GTP-Binding Protein alpha Subunits, Gi-Go - genetics; GTP-Binding Protein alpha Subunits, Gi-Go - metabolism; GTP-Binding Protein alpha Subunits, Gq-G11 - genetics; GTP-Binding Protein alpha Subunits, Gq-G11 - metabolism; HEK293 Cells; Humans; Ligands; Mutation; Naphthalenes - pharmacology; Phenethylamines - pharmacology; Propylamines - pharmacology; Protein Transport; Receptors, Calcium-Sensing - genetics; Receptors, Calcium-Sensing - metabolism
• ISSN: 0026-895X; 1521-0111
• DOI: 10.1124/mol.119.116772

G protein-coupled receptor (GPCR) internalization is crucial for the termination of GPCR activity, and in some cases is associated with G protein-independent signaling and endosomal receptor signaling. To date, internalization has been studied in great detail for class A GPCRs; whereas it is not well established to what extent the observations can be generalized to class C GPCRs, including the extracellular calcium-sensing receptor (CaSR). The CaSR is a prototypical class C GPCR that maintains stable blood calcium (Ca ) levels by sensing minute changes in extracellular free Ca It is thus necessary that the activity of the CaSR is tightly regulated, even while continuously being exposed to its endogenous agonist. Previous studies have used overexpression of intracellular proteins involved in GPCR trafficking, pathway inhibitors, and cell-surface expression or functional desensitization as indirect measures to investigate CaSR internalization. However, there is no general consensus on the processes involved, and the mechanism of CaSR internalization remains poorly understood. The current study provides new insights into the internalization mechanism of the CaSR. We have used a state-of-the-art time-resolved fluorescence resonance energy transfer-based internalization assay to directly measure CaSR internalization in real-time. We demonstrate that the CaSR displays both constitutive and concentration-dependent Ca -mediated internalization. For the first time, we conclusively show that CaSR internalization is sensitive to immediate positive and negative modulation by the CaSR-specific allosteric modulators -(3-[2-chlorophenyl]propyl)-( )- -methyl-3-methoxybenzylamine (NPS R-568) and 2-chloro-6-[(2 )-2-hydroxy-3-[(2-methyl-1-naphthalen-2-ylpropan-2-yl)amino]propoxy]benzonitrile (NPS 2143), respectively. In addition, we provide compelling evidence that CaSR internalization is -arrestin-dependent while interestingly being largely independent of G and G protein signaling. SIGNIFICANCE STATEMENT: A novel highly efficient cell-based real-time internalization assay to show that calcium-sensing receptor (CaSR) internalization is β-arrestin-dependent and sensitive to modulation by allosteric ligands.