Identification of phospholipase D (PLD) activity in mouse peritoneal macrophages

• Published in: Agents and Actions Vol. 39 Spec No; no. S1; pp. C14 - C16
• Main Authors: Meats, J E, Steele, L, Bowen, J G
• Format: Journal Article
• Language: English
• Published: Switzerland 01-01-1993
• Subjects: Animals; Calcimycin - pharmacology; Cells, Cultured; Chromatography, Thin Layer; Glycerophospholipids; Lipopolysaccharides - pharmacology; Macrophages, Peritoneal - enzymology; Mice; Phosphatidic Acids - metabolism; Phospholipase D - metabolism; Platelet Activating Factor - pharmacology; Tetradecanoylphorbol Acetate - pharmacology; Zymosan - pharmacology
• ISSN: 0065-4299; 1420-908X
• DOI: 10.1007/BF01972706

It is now believed that PLD may contribute to the sustained generation of diacylglycerol (DAG) within activated cells. DAG can be formed from phosphatidylcholine by the sequential actions of PLD and phosphatidic acid phosphohydrolase. Phorbal myristate acetate (PMA, 1 microM), A23187 (10 microM) or platelet-activating factor (PAF, 100 nM) caused significant enhancement of intracellular 14C-phosphatidic acid levels 2-5 min after the addition of stimulus, in cultures of peritoneal macrophages pre-labelled with 14C-palmitate. Bacterial lipopolysaccharide (LPS) (5 micrograms/ml) or zymosan (375 micrograms/ml) also stimulated the production of 14C-phosphatidic acid, but over a longer time course (15-60 min). In the presence of 1% ethanol each stimulus caused significant production of 4C-phosphatidylethanol at the expense of 14C-phosphatidic acid, thus confirming a contribution of PLD in these reactions. This is the first report of PLD activity in this cell type.