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磷脂酶D衍生的二酰基甘油在人中性粒细胞呼吸爆发氧化酶激活中的作用。磷脂酸磷酸水解酶抑制剂的抑制作用。

Role of phospholipase D-derived diradylglycerol in the activation of the human neutrophil respiratory burst oxidase. Inhibition by phosphatidic acid phosphohydrolase inhibitors.

作者信息

Perry D K, Hand W L, Edmondson D E, Lambeth J D

机构信息

Department of Biochemistry, Emory University Medical School, Atlanta, GA 30322.

出版信息

J Immunol. 1992 Oct 15;149(8):2749-58.

PMID:1328385
Abstract

An agonist-activated phospholipase D/phosphatidic acid phosphohydrolase (PAH) pathway was recently demonstrated in human neutrophils, and evidence suggests that phosphatidic acid (PA) and/or diradylglycerol (DG) generated from this pathway participates in activation of the O2(-)-generating respiratory burst. We have used a series of cationic amphiphilic compounds (sphingosine, propranolol, chlorpromazine, and desipramine) and antibiotics (clindamycin, trimethoprim, and roxithromycin) all of which inhibit the respiratory burst, to investigate the role of the phospholipase D/PAH pathway in neutrophil activation. The phosphatidylcholine (PC) pool in intact cells was first labeled using [3H]-1-O-alkyl-lysoPC; released [3H]-PA and [3H]-DG were then quantified after the addition of either chemo-attractant or PMA. Using either agonist, all compounds showed a dose-dependent inhibition of [3H]-DG generation which correlated with inhibition of O2- generation, but compounds failed to inhibit directly the NADPH oxidase in a cell-free system. For either activator, a plot of the ID50 values for O2- generation vs those for DG generation was linear over four orders of magnitude. In many cases, inhibition of [3H]-DG generation corresponded to an increase in [3H]-PA, implicating PAH as the locus of inhibition. Superoxide generation was inhibited under conditions where PA was either elevated or minimally affected. Neither O2- release nor DG generation showed any selectivity for stereoisomers of propranolol, suggesting that this inhibition does not act via a specific binding site on PAH. No evidence was obtained for an effect of the inhibitors on PA mobility as monitored by electron spin resonance studies of spin-labeled PA in a model membrane system. Data are consistent with an effect of the inhibitors at the level of the interaction of PAH with the membrane and/or its substrate. These data imply that DG produced via the phospholipase D/PAH pathway functions in the activation or maintenance of the respiratory burst.

摘要

最近在人类中性粒细胞中证实了一种激动剂激活的磷脂酶 D/磷脂酸磷酸水解酶(PAH)途径,且有证据表明,由该途径产生的磷脂酸(PA)和/或二酰基甘油(DG)参与了产 O₂⁻的呼吸爆发的激活过程。我们使用了一系列均能抑制呼吸爆发的阳离子两亲性化合物(鞘氨醇、普萘洛尔、氯丙嗪和地昔帕明)以及抗生素(克林霉素、甲氧苄啶和罗红霉素),来研究磷脂酶 D/PAH 途径在中性粒细胞激活中的作用。首先用[³H]-1-O-烷基溶血磷脂酰胆碱标记完整细胞中的磷脂酰胆碱(PC)池;然后在添加趋化因子或佛波酯后,对释放的[³H]-PA 和[³H]-DG 进行定量分析。使用任一激动剂时,所有化合物均呈现出对[³H]-DG 生成的剂量依赖性抑制,这与对 O₂⁻生成的抑制相关,但这些化合物在无细胞体系中未能直接抑制 NADPH 氧化酶。对于任一激活剂,O₂⁻生成的半数抑制浓度(ID50)值与 DG 生成的 ID50 值的关系图在四个数量级上呈线性。在许多情况下,对[³H]-DG 生成的抑制对应着[³H]-PA 的增加,这表明 PAH 是抑制作用的位点。在 PA 升高或受影响最小的条件下,超氧化物生成均受到抑制。O₂⁻释放和 DG 生成对普萘洛尔的立体异构体均未表现出任何选择性,这表明这种抑制作用并非通过 PAH 上的特定结合位点起作用。通过对模型膜系统中自旋标记的 PA 进行电子自旋共振研究,未获得抑制剂对 PA 流动性有影响的证据。数据表明抑制剂在 PAH 与膜和/或其底物相互作用的水平上发挥作用。这些数据意味着通过磷脂酶 D/PAH 途径产生的 DG 在呼吸爆发的激活或维持中发挥作用。

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