International Union of Pharmacology. XXXIV. Lysophospholipid receptor nomenclature

Jerold Chun, Edward J Goetzl, Timothy Hla, Yasuyuki Igarashi, Kevin R Lynch, Wouter Moolenaar, Susan Pyne, Gabor Tigyi

Research output: Contribution to journalLiterature review

428 Citations (Scopus)

Abstract

The lysophospholipids, lysophosphatidic acid (LPA) and sphingosine 1-phosphate (S1P), are now recognized as important extracellular signaling molecules. These lipid mediators are pleiotropic; among the most common cellular responses are mitogenesis, cell survival (anti-apoptosis), inhibition of adenylyl cyclase and calcium mobilization. Physiologic events associated with these mediators include platelet aggregation, vasopressor activity, wound healing, immune modulation, and angiogenesis. Many of the actions of LPA and S1P are mediated through a set of eight G protein-coupled receptors. Five of these are S1P-prefering while the remaining three are LPA receptors. These receptors are expressed widely and in aggregate signal through a variety of heterotrimeric G proteins. The lysophospholipid receptor family is referred to commonly as the "Edg" group (e.g., Edg-1, Edg-2, etc.). Herein, the molecular pharmacology of the lysophospholipid receptors is reviewed briefly, and a rational nomenclature for LPA and S1P receptors that is consistent with the International Union of Pharmacology guidelines is proposed.

Original languageEnglish
Pages (from-to)265-269
Number of pages5
JournalPharmacological Reviews
Volume54
Issue number2
Publication statusPublished - Jun 2002

Keywords

  • animals
  • humans
  • international agencies
  • lysophospholipids
  • receptors, cell surface
  • receptors, G-protein-coupled
  • receptors, lysophosphatidic acid
  • receptors, lysophospholipid
  • terminology as topic

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    Chun, J., Goetzl, E. J., Hla, T., Igarashi, Y., Lynch, K. R., Moolenaar, W., ... Tigyi, G. (2002). International Union of Pharmacology. XXXIV. Lysophospholipid receptor nomenclature. Pharmacological Reviews, 54(2), 265-269.