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首页> 外文期刊>The biochemical journal >Biosynthesis of platelet-activating factor by cultured rat Kupffer cells stimulated with calcium ionophore A23187
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Biosynthesis of platelet-activating factor by cultured rat Kupffer cells stimulated with calcium ionophore A23187

机译:钙离子载体A23187刺激的大鼠Kupffer细胞对血小板活化因子的生物合成

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pCultured rat Kupffer cells synthesize and release platelet-activating factor (PAF) when stimulated with calcium ionophore A23187. The production of PAF is concentration- and time-dependent and, based upon [3H]serotonin release assays, approx. 1.0 pmol of PAF is formed per 8 x 10(6) cells during 10 min of ionophore stimulation. It is suggested that Kupffer cells are important cellular components which produce and release PAF in order to facilitate communication between hepatic sinusoidal and parenchymal cells. Further, it is suggested that such mediator production in response to reticulo-endothelial cell stimulation causes the hepatic glycogenolytic response previously in the isolated perfused rat liver./p
机译:当用钙离子载体A23187刺激时,培养的大鼠Kupffer细胞合成并释放血小板活化因子(PAF)。 PAF的产生是浓度和时间依赖性的,根据[3H] 5-羟色胺的释放测定,大约需要3-6小时。在10分钟的离子载体刺激过程中,每8 x 10(6)个细胞形成1.0 pmol PAF。提示枯否细胞是产生和释放PAF的重要细胞成分,以促进肝窦和实质细胞之间的通讯。此外,提示这种对网状内皮细胞刺激的反应介质的产生先前在分离的灌注大鼠肝脏中引起了肝糖原分解反应。

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