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PMID: 16818490 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Endocannabinoid biosynthesis proceeding through glycerophospho-N-acyl ethanolamine and a role for alpha/beta-hydrolase 4 in this pathway.

The Journal of biological chemistry ·Vol. 281 ·No. 36 ·2006-09-08 ·Pages 26465-72

Simon GM, Cravatt BF

Abstract

N-Acyl ethanolamines (NAEs) are a large class of signaling lipids implicated in diverse physiological processes, including nociception, cognition, anxiety, appetite, and inflammation. It has been proposed that NAEs are biosynthesized from their corresponding N-acyl phosphatidylethanolamines (NAPEs) in a single enzymatic step catalyzed by a phospholipase D (NAPE-PLD). The recent generation of NAPE-PLD(-/-) mice has revealed that these animals possess lower brain levels of saturated NAEs but essentially unchanged concentrations of polyunsaturated NAEs, including the endogenous cannabinoid anandamide. These findings suggest the existence of additional enzymatic routes for the production of NAEs in vivo. Here, we report evidence for an alternative pathway for NAE biosynthesis that proceeds through the serine hydrolase-catalyzed double-deacylation of NAPE to generate glycerophospho-NAE, followed by the phosphodiesterase-mediated cleavage of this intermediate to liberate NAE. Furthermore, we describe the functional proteomic isolation and identification of a heretofore uncharacterized enzyme alpha/beta-hydrolase 4 (Abh4) as a lysophospholipase/phospholipase B that selectively hydrolyzes NAPEs and lysoNAPEs. Abh4 accepts lysoNAPEs bearing both saturated and polyunsaturated N-acyl chains as substrates and displays a distribution that closely mirrors lysoNAPE-lipase activity in mouse tissues. These results support the existence of an NAPE-PLD-independent route for NAE biosynthesis and suggest that Abh4 plays a role in this metabolic pathway by acting as a (lyso)NAPE-selective lipase.

MeSH Terms
AlkB Homolog 4, Lysine Demethylase Amino Acid Sequence Animals Cannabinoid Receptor Modulators/biosynthesis Dioxygenases Endocannabinoids Ethanolamines/chemistry,metabolism Glycerophosphates/metabolism Humans Hydrolases/classification,genetics,metabolism Lipase/metabolism Mice Mice, Knockout Molecular Sequence Data Phospholipase D/genetics,metabolism Phospholipases/classification,genetics,metabolism Phylogeny Recombinant Proteins/genetics,metabolism Sequence Alignment Substrate Specificity Tissue Distribution
Chemicals
Cannabinoid Receptor Modulators Endocannabinoids Ethanolamines Glycerophosphates N-acylethanolamines Recombinant Proteins Dioxygenases ALKBH4 protein, mouse AlkB Homolog 4, Lysine Demethylase Hydrolases Phospholipases Lipase N-acylphosphatidylethanolamine phospholipase D, mouse Phospholipase D
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Simon Gabriel M
Skaggs Institute for Chemical Biology and Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Cravatt Benjamin F
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2006-09-08
Epub
2006-00-03
Pages
26465-72
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDA NIH HHS · DA015197 · United States
NIDA NIH HHS · R01 DA015197 · United States
NIDA NIH HHS · DA017259 · United States
NIDA NIH HHS · P01 DA017259 · United States
NIDA NIH HHS · P01 DA017259-03 · United States
NIDA NIH HHS · R01 DA015197-04 · United States
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