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缓激肽对猪主动脉内皮细胞中肌醇多磷酸生成的刺激作用。

Bradykinin stimulation of inositol polyphosphate production in porcine aortic endothelial cells.

作者信息

Lambert T L, Kent R S, Whorton A R

出版信息

J Biol Chem. 1986 Nov 15;261(32):15288-93.

PMID:3771575
Abstract

Bradykinin stimulation of inositol polyphosphate production was followed using [3H]inositol-labeled porcine aortic endothelial cells grown in culture. Bradykinin stimulated a significant increase in inositol trisphosphate (IP3) production within 15 s. This increase reached a maximum value of 5-fold above control at 30 s and returned toward baseline by 90 s. Production of inositol bisphosphate increased with time reaching 4-fold by 60 s. Bradykinin stimulated the production of IP3 and inositol biphosphate in a dose-dependent manner with an EC50 of 9 X 10(-9) M. Labeled pools of phosphatidylinositol-4,5-bisphosphate (PIPP) decreased by 50% within 30 s, corresponding to the rise in IP3, while labeled lysophosphatidylinositol pools increased 3-fold by 60 s. Pertussis toxin, a protein which ribosylates GTP-binding proteins, did not inhibit bradykinin-stimulated inositol polyphosphate production. Incubation of labeled cells in the absence of extracellular Ca2+ also did not affect bradykinin-stimulated inositol polyphosphate production. Further, A23187, a Ca2+ ionophore, failed to stimulate PIPP metabolism. Finally, Ca2+ influx into cell monolayers occurred with a time course which paralleled rather than preceded the increase in IP3 levels. These data suggest that bradykinin stimulates phospholipase C metabolism of PIPP to IP3 by a mechanism which does not contain a pertussis toxin sensitive GTP-binding protein. Also, this receptor-linked phospholipase C activity does not appear to be activated by extracellular Ca2+ influx. The results support the proposal that IP3 production initiates Ca2+ mobilization and suggest that the calcium-dependent step in arachidonate release is distal to IP3 production.

摘要

使用培养的[3H]肌醇标记的猪主动脉内皮细胞,观察缓激肽刺激肌醇多磷酸产生的情况。缓激肽在15秒内刺激肌醇三磷酸(IP3)产生显著增加。这种增加在30秒时达到比对照高5倍的最大值,并在90秒时恢复到基线水平。肌醇二磷酸的产生随时间增加,到60秒时达到4倍。缓激肽以剂量依赖方式刺激IP3和肌醇二磷酸的产生,半数有效浓度(EC50)为9×10(-9)M。磷脂酰肌醇-4,5-二磷酸(PIPP)的标记池在30秒内减少50%,与IP3的升高相对应,而标记的溶血磷脂酰肌醇池在60秒时增加3倍。百日咳毒素是一种使GTP结合蛋白核糖基化的蛋白质,它不抑制缓激肽刺激的肌醇多磷酸产生。在无细胞外Ca2+的情况下孵育标记细胞也不影响缓激肽刺激的肌醇多磷酸产生。此外,Ca2+离子载体A23187未能刺激PIPP代谢。最后,Ca2+流入细胞单层的时间进程与IP3水平的增加平行,而不是先于IP3水平的增加。这些数据表明,缓激肽通过一种不包含对百日咳毒素敏感的GTP结合蛋白的机制刺激PIPP的磷脂酶C代谢为IP3。而且,这种受体连接的磷脂酶C活性似乎不是由细胞外Ca2+流入激活的。结果支持IP3产生启动Ca2+动员的观点,并表明花生四烯酸释放中依赖钙的步骤在IP3产生之后。

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