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组胺介导的前列环素在培养的人血管内皮细胞中的合成调控

Regulation of histamine-mediated prostacyclin synthesis in cultured human vascular endothelial cells.

作者信息

Baenziger N L, Fogerty F J, Mertz L F, Chernuta L F

出版信息

Cell. 1981 Jun;24(3):915-23. doi: 10.1016/0092-8674(81)90117-3.

Abstract

Histamine stimulates the production of prostacyclin (PGI2) in cultured human endothelial cells. We have examined the cell specificity of histamine-mediated PGI2 synthesis in primary and subcultured human cells. Venous and arterial smooth muscle cells and skin fibroblasts synthesized PGI2 from exogenous arachidonic acid, but they did not synthesize a significant amount of PGI2 when treated with histamine. Endothelial cells, however, produced similar amounts of PGI2 in response to histamine and arachidonic acid. Thrombin also stimulates PGI2 production in endothelial cells. Histamine and thrombin yielded an additive production of PGI2 when added simultaneously to endothelial cells. When histamine and thrombin were added sequentially, the amount of PGI2 produced was not additive but equaled the amount characteristic of the first agonist alone. Following an initial treatment with histamine, endothelial cells were unable to respond to histamine for 3 hr, after which the PGI2 biosynthetic response rapidly returned to normal by 4 1/2 hr. When the initial histamine treatment was carried out under mildly alkaline conditions, the complete return of activity was delayed to 8 hr after treatment. The synthesis of PGI2 from exogenous arachidonic acid was unaffected by prior treatment with histamine. Recovery of histamine-mediated PGI2 production was not dependent on protein synthesis but required a component of fetal calf serum that is nondialyzable and moderately heat stable. Thus endothelial cell PGI2 synthesis in responses to a physiologic agonist is subject to several levels of regulation, reflecting not only intracellular events but also the extracellular environment.

摘要

组胺可刺激培养的人内皮细胞合成前列环素(PGI2)。我们已经研究了组胺介导的PGI2合成在原代和传代培养的人细胞中的细胞特异性。静脉和动脉平滑肌细胞以及皮肤成纤维细胞可从外源性花生四烯酸合成PGI2,但用组胺处理时它们不会合成大量的PGI2。然而,内皮细胞对组胺和花生四烯酸的反应产生的PGI2量相似。凝血酶也可刺激内皮细胞产生PGI2。当组胺和凝血酶同时添加到内皮细胞时,它们对PGI2的产生具有累加作用。当组胺和凝血酶依次添加时,产生的PGI2量并非累加,而是等于单独使用第一种激动剂时的特征量。在用组胺进行初始处理后,内皮细胞在3小时内无法对组胺作出反应,此后PGI2生物合成反应在4.5小时迅速恢复正常。当初始组胺处理在轻度碱性条件下进行时,活性完全恢复延迟至处理后8小时。从外源性花生四烯酸合成PGI2不受组胺预处理的影响。组胺介导的PGI2产生的恢复不依赖于蛋白质合成,但需要胎牛血清中的一种不可透析且中度热稳定的成分。因此,内皮细胞对生理激动剂反应中的PGI2合成受到多个水平的调节,这不仅反映了细胞内事件,也反映了细胞外环境。

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