Ohtsuka T, Ozawa M, Okamura N, Ishibashi S
Department of Physiological Chemistry, Hiroshima University School of Medicine.
J Biochem. 1989 Aug;106(2):259-63. doi: 10.1093/oxfordjournals.jbchem.a122841.
Treatment of guinea pig polymorphonuclear leukocytes (PMNL) with a phosphatidate containing short-chain fatty acids, 1,2-didecanoyl-3-sn-phosphatidate (PA10), induced substantial superoxide anion (O2-) production in a dose-dependent manner, whereas phosphatidates prepared from egg lecithin and 1,2-dioleoyl-3-sn-phosphatidate (PA18:1) had no such effect. Calcium was not involved in PA10-induced O2- production, since the production was also observed in the case of addition of EGTA prior to PA10 or pretreatment of PMNL with quin-2 and EGTA to eliminate contributions of both extracellular and intracellular calcium. We have reported in previous papers that the phosphorylation of 46K protein(s), which was commonly observed in parallel with an activation of NADPH oxidase in PMNL, was increased by treatment with 10 microM 1-oleoyl-2-acetylglycerol (OAG) with little change in the O2- production (Okamura et al. (1984) Arch. Biochem. Biophys. 228, 270-277; Ohtsuka et al. (1988) Arch. Biochem. Biophys. 260, 226-231). Treatment of PMNL with a combination of PA10, which slightly increased 46K protein phosphorylation, and such a low concentration of OAG induced a marked increase in the O2- production with the increase in 46K protein phosphorylation, which was probably due to OAG action. Thus, it is likely that this protein phosphorylation plays a significant role in the stimulation of the O2- production by phosphatidate in PMNL.
用含短链脂肪酸的磷脂酸,即1,2 - 二癸酰 - 3 - sn - 磷脂酸(PA10)处理豚鼠多形核白细胞(PMNL),会以剂量依赖的方式诱导大量超氧阴离子(O2-)产生,而由卵磷脂和1,2 - 二油酰 - 3 - sn - 磷脂酸(PA18:1)制备的磷脂酸则没有这种作用。钙不参与PA10诱导的O2-产生,因为在PA10之前添加乙二醇双(2 - 氨基乙醚)四乙酸(EGTA)或用喹啉 - 2和EGTA预处理PMNL以消除细胞外和细胞内钙的贡献的情况下,也观察到了这种产生。我们在之前的论文中报道过,在PMNL中与烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶激活同时普遍观察到的46K蛋白的磷酸化,在用10微摩尔1 - 油酰 - 2 - 乙酰甘油(OAG)处理时增加,而O2-产生变化不大(冈村等人(1984年)《生物化学与生物物理学文献》228卷,第270 - 277页;大冢等人(1988年)《生物化学与生物物理学文献》260卷,第226 - 231页)。用略微增加46K蛋白磷酸化的PA10与如此低浓度的OAG组合处理PMNL,会导致O2-产生显著增加,同时46K蛋白磷酸化增加,这可能是由于OAG的作用。因此,这种蛋白磷酸化可能在磷脂酸刺激PMNL产生O2-中起重要作用。