Tamura M, Ogata K, Takeshita M
Department of Applied Chemistry, Faculty of Engineering, Ehime University, Japan.
Arch Biochem Biophys. 1993 Sep;305(2):477-82. doi: 10.1006/abbi.1993.1450.
The ability of phosphatidic acid to induce O2- generation was examined in intact and electropermeabilized neutrophils. In intact cells, after a long lag (approximately 11 min), 1,2-didecanoylphosphatidic acid (PA10, 10 microM) elicited O2- generation (30-40 nmol/min/10(7) cells at maximum) which lasted for 8-9 min. Electropermeabilization facilitated the response by shortening the lag (within 30 s) and enhancing the maximal rate (120-130 O2- nmol/min/10(7) cells). The induction by PA10 was concentration-dependent and the half-maximal concentrations for intact and permeabilized cells were 11 and 3 microM, respectively. In permeabilized cells, the rate of O2- release by PA10, which was similar to that by fMet-Leu-Phe or phorbol myristate acetate, was not enhanced by addition of dioctanoylglycerol. Also, the response was unaffected by propranolol, an inhibitor of phosphatidate-phosphohydrolase that converts phosphatidic acid to diacylglycerol. Phosphatidic acids with longer acyl chains (C12-C14) also activated the permeabilized cells, although the degree of activation decreased as the chain length was increased. These results indicate the ability of phosphatidic acid to induce respiratory burst independently of diacylglycerol and support the idea that phosphatidic acid can be an activator of NADPH oxidase in human neutrophils.
