Lysophospholipid acyltransferases: novel potential regulators of the inflammatory response and target for new drug discovery.

Abstract

Molecular and biochemical analyses of membrane phospholipids have revealed that, in addition to their physico-chemical properties, the metabolites of phospholipids play a crucial role in the recognition, signalling and responses of cells to a variety of stimuli. Such responses are mediated in large part by the removal and/or addition of different acyl chains to provide different phospholipid molecular species. The reacylation reactions, catalysed by specific acyltransferases control phospholipid composition and the availability of the important mediators free arachidonic acid and lysophospholipids. Lysophospholipid acyltransferases are therefore key control points for cellular responses to a variety of stimuli including inflammation. Regulation or manipulation of lysophospholipid acyltransferases may thus provide important mechanisms for novel anti-inflammatory therapies. This review will highlight mammalian lysophospholipid acyltransferases with particular reference to the potential role of lysophosphatidylcholine acyltransferase and its substrates in sepsis and other inflammatory conditions and as a potential target for novel anti-inflammatory therapies.

• Authors: Simon K Jackson, Wondwossen Abate, Amanda J Tonks
• Journal: Pharmacology & therapeutics (Pharmacol Ther) Vol. 119 Issue 1 Pg. 104-14 (Jul 2008) ISSN: 0163-7258 [Print] England
• PMID: 18538854 (Publication Type: Journal Article, Review)

Chemical References

• Enzyme Inhibitors
• Lipopolysaccharides
• Lysophosphatidylcholines
• Phospholipids
• Interferon-gamma
• 1-Acylglycerophosphocholine O-Acyltransferase

Topics

• 1-Acylglycerophosphocholine O-Acyltransferase (antagonists & inhibitors, physiology)
• Amino Acid Sequence
• Animals
• Apoptosis
• Brain Injuries (metabolism)
• Drug Discovery
• Enzyme Inhibitors (therapeutic use)
• Humans
• Inflammation (enzymology, etiology)
• Interferon-gamma (pharmacology)
• Lipopolysaccharides (toxicity)
• Lysophosphatidylcholines (metabolism)
• Molecular Sequence Data
• Monocytes (drug effects, metabolism)
• Phospholipids (metabolism)
• Sepsis (drug therapy, metabolism)