Rossi F, Grzeskowiak M, Della Bianca V, Calzetti F, Gandini G
Institute of General Pathology, University of Verona, Italy.
Biochem Biophys Res Commun. 1990 Apr 16;168(1):320-7. doi: 10.1016/0006-291x(90)91711-z.
It is widely accepted that the activation of the NADPH oxidase of phagocytes is linked to the stimulation of protein kinase C by diacylglycerol formed by hydrolysis of phospholipids. The main source would be choline containing phospholipid via phospholipase D and phosphatidate phosphohydrolase. This paper presents a condition where the activation of the respiratory burst by FMLP correlates with the formation of phosphatidic acid, via phospholipase D, and not with that of diacylglycerol. In fact: 1) in neutrophils treated with propranolol, an inhibitor of phosphatidate phosphohydrolase, FMLP plus cytochalasin B induces a respiratory burst associated with a stimulation of phospholipase D, formation of phosphatidic acid and complete inhibition of that of diacylglycerol. 2) The respiratory burst by FMLP plus cytochalasin B lasts a few minutes and may be restimulated by propranolol which induces an accumulation of phosphatidic acid. 3) In neutrophils stimulated by FMLP in the absence of cytochalasin B propranolol causes an accumulation of phosphatidic acid and a marked enhancement of the respiratory burst without formation of diacylglycerol. 4) The inhibition of the formation of phosphatidic acid via phospholipase D by butanol inhibits the respiratory burst by FMLP.
人们普遍认为,吞噬细胞的NADPH氧化酶激活与磷脂水解形成的二酰甘油对蛋白激酶C的刺激有关。主要来源可能是通过磷脂酶D和磷脂酸磷酸水解酶作用的含胆碱磷脂。本文提出了一种情况,即FMLP引发的呼吸爆发激活与通过磷脂酶D形成磷脂酸相关,而与二酰甘油的形成无关。事实上:1)在用磷脂酸磷酸水解酶抑制剂普萘洛尔处理的中性粒细胞中,FMLP加细胞松弛素B诱导呼吸爆发,同时伴有磷脂酶D的刺激、磷脂酸的形成以及二酰甘油形成的完全抑制。2)FMLP加细胞松弛素B引发的呼吸爆发持续几分钟,普萘洛尔可再次刺激其发生,普萘洛尔会诱导磷脂酸积累。3)在无细胞松弛素B的情况下,FMLP刺激的中性粒细胞中,普萘洛尔会导致磷脂酸积累,并显著增强呼吸爆发,且不会形成二酰甘油。4)丁醇通过抑制磷脂酶D对磷脂酸形成的作用,抑制了FMLP引发的呼吸爆发。