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白细胞介素1和肿瘤坏死因子对MDCK细胞中前列腺素E2合成的刺激作用,以及环己酰亚胺对该作用的增强作用。

Interleukin 1- and tumor necrosis factor-stimulation of prostaglandin E2 synthesis in MDCK cells, and potentiation of this effect by cycloheximide.

作者信息

Leighton J D, Pfeilschifter J

机构信息

Research Department, Ciba-Geigy AG, Basel, Switzerland.

出版信息

FEBS Lett. 1990 Jan 1;259(2):289-92. doi: 10.1016/0014-5793(90)80029-i.

Abstract

The effects of interleukin (IL)-1 alpha, IL-1 beta and TNF alpha on prostaglandin-E2 synthesis in Madin-Darby canine kidney (MDCK) cells were investigated. IL-1 beta time- and dose-dependently stimulated prostaglandin-E2 synthesis. While TNF alpha produced a comparatively small but significant stimulation of PGE2 release, coincubation of IL-1 beta with TNF alpha produced a marked synergistic stimulation of PGE2 release. The effect of IL-1 beta and of IL-1 beta and TNF alpha was apparent as early as after 2 h of incubation. The enhanced PGE2 synthesis was inhibited by indomethacin as well as actinomycin D, while cycloheximide surprisingly potentiated PGE2 synthesis in response to both IL-1 beta and TNF alpha. IL-1 alpha alone was ineffective in stimulating a significant release of PGE2 at concentrations as high as 10 nM. However, it also showed a marked synergistic interaction with TNF alpha in stimulating PGE2 release.

摘要

研究了白细胞介素(IL)-1α、IL-1β和肿瘤坏死因子α(TNFα)对犬肾传代细胞(MDCK)中前列腺素E2合成的影响。IL-1β对前列腺素E2合成的刺激具有时间和剂量依赖性。虽然TNFα对前列腺素E2(PGE2)释放产生相对较小但显著的刺激作用,但IL-1β与TNFα共同孵育可显著协同刺激PGE2释放。IL-1β以及IL-1β与TNFα共同作用的效应早在孵育2小时后就很明显。吲哚美辛和放线菌素D可抑制PGE2合成增强,而环己酰亚胺出人意料地增强了对IL-1β和TNFα刺激的PGE2合成。单独的IL-1α在高达10 nM的浓度下刺激PGE2显著释放无效。然而,它在刺激PGE2释放方面也与TNFα表现出明显的协同相互作用。

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