Emerging lysophospholipid mediators, lysophosphatidylserine, lysophosphatidylthreonine, lysophosphatidylethanolamine and lysophosphatidylglycerol

Prostaglandins Other Lipid Mediat. 2009 Sep;89(3-4):135-9. doi: 10.1016/j.prostaglandins.2009.04.009. Epub 2009 May 7.

Abstract

It is now widely accepted that lysophospholipids (LPLs), a product of the phospholipase A reaction, function as mediators through G-protein-coupled receptors. Notably, recent studies of lysophosphatidic acid (LPA) and sphingosine 1-phosphate (S1P) have revealed their essential roles in vivo. On the other hand, other LPLs such as lysophosphatidylserine (LPS), lysophosphatidylthreonine (LPT), lysophosphatidylethanolamine (LPE), lysophosphatidylinositol (LPI) and lysophosphatidylglycerol (LPG) have been reported to show lipid mediator-like responses both in vivo (LPS and LPT) and in vitro (LPS, LPT, LPE and LPG), while very little is known about their receptor, synthetic enzyme and patho-physiological roles. In this review, we summarize the actions of these LPLs as lipid mediators including LPS, LPT, LPE and LPG.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Humans
  • Ligands
  • Lysophospholipids / physiology*
  • Protein Isoforms
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, G-Protein-Coupled / physiology
  • Receptors, Lysophospholipid / chemistry
  • Receptors, Lysophospholipid / physiology
  • Signal Transduction

Substances

  • G-protein-coupled receptor 34
  • Ligands
  • Lysophospholipids
  • Protein Isoforms
  • Receptors, G-Protein-Coupled
  • Receptors, Lysophospholipid