Cells · 2023 · 12 citations · 23 references
Life SciencesMolecular BiologyPharmacologyCell SignalingMolecular Cell BiologySignal TransductionCell Adhesion ReceptorsCell Signaling NetworksCell Surface Receptor SignalingExtracellular MatrixG Protein-coupled Receptor SignalingReceptor RegulationAdhesion ReceptorsCancer Cell Proliferation InhibitionG Protein-coupled Receptor ActivationG Protein-coupled Receptor BindingG Protein-coupled Receptor RegulationG Protein-coupled SignalingG-protein-coupled ReceptorsReceptor Splice Variants
GPR126/ADGRG6, a member of the adhesion G-protein-coupled receptor family, balances cell differentiation and proliferation through fine-tuning of intracellular cAMP levels, which is achieved through coupling to Gs and Gi proteins. While GPR126-mediated cAMP increase has been proven to be essential for differentiation of Schwann cells, adipocytes and osteoblasts, Gi-signaling of the receptor was found to propagate breast cancer cell proliferation. Extracellular ligands or mechanical forces can modulate GPR126 activity but require an intact encrypted agonist sequence, coined the Stachel. Even though coupling to Gi can be seen for constitutively active truncated receptor versions of GPR126 as well as with a peptide agonist derived from the Stachel sequence, all known N-terminal modulators have so far only been shown to modulate Gs coupling. Here, we identified collagen VI as the first extracellular matrix ligand of GPR126 that induces Gi signaling at the receptor, which shows that N-terminal binding partners can mediate selective G protein signaling cascades that are masked by fully active truncated receptor variants.
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Substitution of three amino acids switches receptor specificity of Gqα to that of Giα
Bruce R. Conklin, Zvi Farfel, Kevin D. Lustig et al. · Nature · 1993 · 736 citations
A G Protein–Coupled Receptor Is Essential for Schwann Cells to Initiate Myelination
Kelly R. Monk, Stephen G. Naylor, Thomas D. Glenn et al. · Science · 2009 · 327 citations · Full text