N-acylphosphatidylethanolamine-hydrolysing phospholipase D lacks the ability to transphosphatidylate

被引:62
作者
Petersen, G [1 ]
Hansen, HS [1 ]
机构
[1] Royal Danish Sch Pharm, Dept Pharmacol, DK-2100 Copenhagen, Denmark
关键词
phospholipase D; N-acylphosphatidylethanolamine; N-acylethanolamine; anandamide; transphosphatidylation;
D O I
10.1016/S0014-5793(99)00861-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The N-acylphosphatidylethanolamine-hydrolysing phospholipase D (NAPE-PLD) generates N-acylethanolamines, including N-arachidonoyl-ethanolamine (anandamide), that may be neuroprotective and analgesic. The properties of NAPE-PLD from rat heart and brain microsomes are investigated and compared to those of other PLDs. NAPE-PLD is inhibited by the fatty acid aminohydrolase inhibitor MAFP in high concentrations (greater than or equal to.100 mu M) while PMSF in high concentrations (10 mM) tends to stabilise NAPE-PLD activity. Oleate inhibits NAPE-FED but the enzyme is not affected by PIP2, alpha-synuclein or mastoparan. Furthermore, it is for the first time reported that NAPE-PLD is not capable of catalysing a transphosphatidylation reaction like most other known PLDs. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:41 / 44
页数:4
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共 43 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   Control of pain initiation by endogenous cannabinoids [J].
Calignano, A ;
La Rana, G ;
Giuffrida, A ;
Piomelli, D .
NATURE, 1998, 394 (6690) :277-281
[3]   LIPID SIGNALING ENZYMES AND SURFACE DILUTION KINETICS [J].
CARMAN, GM ;
DEEMS, RA ;
DENNIS, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (32) :18711-18714
[4]   FATTY-ACID ACTIVATION AND TEMPERATURE PERTURBATION OF RAT-BRAIN MICROSOMAL PHOSPHOLIPASE-D [J].
CHALIFOUR, R ;
KANFER, JN .
JOURNAL OF NEUROCHEMISTRY, 1982, 39 (02) :299-305
[5]   N-acylethanolamines:: Formation and molecular composition of a new class of plant lipids [J].
Chapman, KD ;
Tripathy, S ;
Venables, B ;
Desouza, AD .
PLANT PHYSIOLOGY, 1998, 116 (03) :1163-1168
[6]   Phospholipase D2, a distinct phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization [J].
Colley, WC ;
Sung, TC ;
Roll, R ;
Jenco, J ;
Hammond, SM ;
Altshuller, Y ;
BarSagi, D ;
Morris, AJ ;
Frohman, MA .
CURRENT BIOLOGY, 1997, 7 (03) :191-201
[8]   Novel inhibitors of brain, neuronal, and basophilic anandamide amidohydrolase [J].
DePetrocellis, L ;
Melck, D ;
Ueda, N ;
Maurelli, S ;
Kurahashi, Y ;
Yamamoto, S ;
Marino, G ;
DiMarzo, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (01) :82-88
[9]   Methyl arachidonyl fluorophosphonate: A potent irreversible inhibitor of anandamide amidase [J].
Deutsch, DG ;
Omeir, R ;
Arreaza, G ;
Salehani, D ;
Prestwich, GD ;
Huang, Z ;
Howlett, A .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (03) :255-260
[10]   ENZYMATIC-SYNTHESIS AND DEGRADATION OF ANANDAMIDE, A CANNABINOID RECEPTOR AGONIST [J].
DEUTSCH, DG ;
CHIN, SA .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (05) :791-796