TY - JOUR T1 - Adhesion G Protein–Coupled Receptors: From In Vitro Pharmacology to In Vivo Mechanisms JF - Molecular Pharmacology JO - Mol Pharmacol SP - 617 LP - 623 DO - 10.1124/mol.115.098749 VL - 88 IS - 3 AU - Kelly R. Monk AU - Jörg Hamann AU - Tobias Langenhan AU - Saskia Nijmeijer AU - Torsten Schöneberg AU - Ines Liebscher Y1 - 2015/09/01 UR - http://molpharm.aspetjournals.org/content/88/3/617.abstract N2 - The adhesion family of G protein–coupled receptors (aGPCRs) comprises 33 members in humans. aGPCRs are characterized by their enormous size and complex modular structures. While the physiologic importance of many aGPCRs has been clearly demonstrated in recent years, the underlying molecular functions have only recently begun to be elucidated. In this minireview, we present an overview of our current knowledge on aGPCR activation and signal transduction with a focus on the latest findings regarding the interplay between ligand binding, mechanical force, and the tethered agonistic Stachel sequence, as well as implications on translational approaches that may derive from understanding aGPCR pharmacology. ER -