Phospholipid and arachidonic acid metabolism in zymosan-stimulated human monocytes: modulation by cAMP

• Published in: Journal of cellular physiology Vol. 131; no. 3; p. 384
• Main Authors: Godfrey, R W, Manzi, R M, Gennaro, D E, Hoffstein, S T
• Format: Journal Article
• Language: English
• Published: United States 01.06.1987
• Subjects: 1-Methyl-3-isobutylxanthine - pharmacology; Arachidonic Acid; Arachidonic Acids - metabolism; Arachidonic Acids - secretion; Bucladesine - pharmacology; Cyclic AMP - pharmacology; Humans; Lysosomes - enzymology; Lysosomes - secretion; Membrane Lipids - metabolism; Monocytes - drug effects; Monocytes - metabolism; Monocytes - secretion; Phospholipases A - metabolism; Phospholipids - metabolism; Phospholipids - secretion; Type C Phospholipases - metabolism; Zymosan - pharmacology
• ISSN: 0021-9541
• DOI: 10.1002/jcp.1041310310

Receptor-ligand interaction in mononuclear phagocytes is intimately linked to alterations in membrane phospholipids and release of arachidonic acid (AA). In addition, synthesis of bioactive lipids from released AA can result in further modification of cell responses. Upon challenge with opsonized zymosan, [3H]-arachidonic acid ([3H]-AA)-labeled human monocytes released 25 +/- 2% of their incorporated radiolabel within 30 min. Pretreatment of the monocytes with 5 X 10(-4) M isobutylmethylxanthine (IBMX) or 1 X 10(-3) M dibutyryl cyclic AMP (d-cAMP) inhibited total [3H]-AA release in the presence of zymosan by 47% and 42%, respectively. Analysis of incorporated [3H]-AA in cellular phospholipid pools indicated that significant amounts of label were lost from both phosphatidylcholine (PC) and phosphatidylinositol (PI) during zymosan stimulation. Treatment with d-cAMP substantially inhibited the loss of label from PC, but had no affect on PI. HPLC analysis of cell supernatants from zymosan-treated cells indicated that 5-HETE was the predominant metabolite generated from [3H]-AA, and its production was depressed during treatment with d-cAMP. Phospholipase activity in human monocyte homogenates was not effected by d-cAMP or IBMX at the highest concentrations used, whether these were added directly to the homogenate or by pretreatment of whole cells, demonstrating that inhibition required an intact cell. These results suggest that human monocytes exposed to opsonized zymosan release AA via two mechanisms and that modulation by cAMP is indirectly effecting a phospholipase directed towards PC.