International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors.

نویسندگان

  • Jörg Hamann
  • Gabriela Aust
  • Demet Araç
  • Felix B Engel
  • Caroline Formstone
  • Robert Fredriksson
  • Randy A Hall
  • Breanne L Harty
  • Christiane Kirchhoff
  • Barbara Knapp
  • Arunkumar Krishnan
  • Ines Liebscher
  • Hsi-Hsien Lin
  • David C Martinelli
  • Kelly R Monk
  • Miriam C Peeters
  • Xianhua Piao
  • Simone Prömel
  • Torsten Schöneberg
  • Thue W Schwartz
  • Kathleen Singer
  • Martin Stacey
  • Yuri A Ushkaryov
  • Mario Vallon
  • Uwe Wolfrum
  • Mathew W Wright
  • Lei Xu
  • Tobias Langenhan
  • Helgi B Schiöth
چکیده

The Adhesion family forms a large branch of the pharmacologically important superfamily of G protein-coupled receptors (GPCRs). As Adhesion GPCRs increasingly receive attention from a wide spectrum of biomedical fields, the Adhesion GPCR Consortium, together with the International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug Classification, proposes a unified nomenclature for Adhesion GPCRs. The new names have ADGR as common dominator followed by a letter and a number to denote each subfamily and subtype, respectively. The new names, with old and alternative names within parentheses, are: ADGRA1 (GPR123), ADGRA2 (GPR124), ADGRA3 (GPR125), ADGRB1 (BAI1), ADGRB2 (BAI2), ADGRB3 (BAI3), ADGRC1 (CELSR1), ADGRC2 (CELSR2), ADGRC3 (CELSR3), ADGRD1 (GPR133), ADGRD2 (GPR144), ADGRE1 (EMR1, F4/80), ADGRE2 (EMR2), ADGRE3 (EMR3), ADGRE4 (EMR4), ADGRE5 (CD97), ADGRF1 (GPR110), ADGRF2 (GPR111), ADGRF3 (GPR113), ADGRF4 (GPR115), ADGRF5 (GPR116, Ig-Hepta), ADGRG1 (GPR56), ADGRG2 (GPR64, HE6), ADGRG3 (GPR97), ADGRG4 (GPR112), ADGRG5 (GPR114), ADGRG6 (GPR126), ADGRG7 (GPR128), ADGRL1 (latrophilin-1, CIRL-1, CL1), ADGRL2 (latrophilin-2, CIRL-2, CL2), ADGRL3 (latrophilin-3, CIRL-3, CL3), ADGRL4 (ELTD1, ETL), and ADGRV1 (VLGR1, GPR98). This review covers all major biologic aspects of Adhesion GPCRs, including evolutionary origins, interaction partners, signaling, expression, physiologic functions, and therapeutic potential.

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عنوان ژورنال:
  • Pharmacological reviews

دوره 67 2  شماره 

صفحات  -

تاریخ انتشار 2015