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表皮生长因子和血管紧张素II刺激肝细胞中肌醇1,4,5-三磷酸和肌醇1,3,4-三磷酸的形成。百日咳毒素和佛波醇12-肉豆蔻酸酯13-乙酸酯的差异抑制作用。

Epidermal growth factor and angiotensin II stimulate formation of inositol 1,4,5- and inositol 1,3,4-trisphosphate in hepatocytes. Differential inhibition by pertussis toxin and phorbol 12-myristate 13-acetate.

作者信息

Johnson R M, Garrison J C

机构信息

Department of Pharmacology, University of Virginia School of Medicine, Charlottesville 22908.

出版信息

J Biol Chem. 1987 Dec 25;262(36):17285-93.

PMID:3500949
Abstract

The ability of epidermal growth factor (EGF) and angiotensin II to stimulate production of inositol trisphosphate and mobilize intracellular Ca2+ in hepatocytes was compared using quin2 fluorescence to monitor changes in Ca2+ levels and high performance liquid chromatography to resolve the inositol trisphosphate (InsP3) isomers. Both EGF and angiotensin II stimulated an increase in free intracellular Ca2+ concentration ([Ca2+]i) as well as a rapid increase in the production of inositol 1,4,5-trisphosphate (Ins(1,4,5)P3). Concentrations of angiotensin II which gave a rise in [Ca2+]i equivalent to that seen with maximal doses of EGF produced an equivalent increase in Ins(1,4,5)P3 formation. Both EGF and angiotensin II stimulated the formation of the Ins(1,3,4)P3 and inositol 1,3,4,5-tetrakisphosphate isomers. The formation of the Ins(1,3,4)P3 isomer lagged behind production of Ins(1,4,5)P3 but eventually reached higher levels in the cell. The initial rise in [Ca2+]i and InsP3 levels stimulated by EGF and angiotensin II was not affected by reducing the external Ca2+ concentration below 30 nM with an excess of [ethylenebis(oxyethylenenitrilo)] tetraacetic acid. Treatment of hepatocytes for 30-180 s with 1 micrograms/ml phorbol 12-myristate 13-acetate prior to the addition of EGF blocked the EGF-stimulated production of Ins(1,4,5)P3 and the increase in [Ca2+]i. Phorbol 12-myristate 13-acetate attenuated the production of Ins(1,4,5)P3 generated by angiotensin II over the concentration range of 10(-10) to 10(-8) M; however, the Ca2+ signal was only inhibited at the 10(-10) M dose of angiotensin II. Treatment of rats with pertussis toxin for 72 h prior to isolating hepatocytes blocked the ability of EGF to increase Ins(1,4,5)P3 and Ins(1,3,4)P3 but did not inhibit the ability of any concentration of angiotensin II to stimulate formation of InsP3 or inositol tetrakisphosphate. The observation that pertussis toxin selectively abolishes EGF-stimulated inositol lipid breakdown suggests that EGF and angiotensin II use different mechanisms to activate phospholipase C in hepatocytes.

摘要

利用喹啉-2荧光监测钙离子水平变化,并采用高效液相色谱法解析肌醇三磷酸(InsP3)异构体,比较了表皮生长因子(EGF)和血管紧张素II刺激肝细胞中肌醇三磷酸生成及动员细胞内钙离子的能力。EGF和血管紧张素II均刺激细胞内游离钙离子浓度([Ca2+]i)升高,以及肌醇1,4,5-三磷酸(Ins(1,4,5)P3)生成迅速增加。能使[Ca2+]i升高至与最大剂量EGF相当水平的血管紧张素II浓度,会使Ins(1,4,5)P3生成量出现同等程度的增加。EGF和血管紧张素II均刺激肌醇1,3,4-三磷酸(Ins(1,3,4)P3)和肌醇1,3,4,5-四磷酸异构体的生成。Ins(1,3,4)P3异构体的生成滞后于Ins(1,4,5)P3,但最终在细胞内达到更高水平。用过量的[乙二胺双(氧乙烯基腈)]四乙酸将细胞外钙离子浓度降至30 nM以下,并不影响EGF和血管紧张素II刺激引起的[Ca2+]i和InsP3水平的初始升高。在添加EGF之前,用1微克/毫升佛波醇12-肉豆蔻酸酯13-乙酸酯处理肝细胞30 - 180秒,可阻断EGF刺激的Ins(1,4,5)P3生成及[Ca2+]i升高。在10^(-10)至10^(-8) M浓度范围内,佛波醇12-肉豆蔻酸酯13-乙酸酯可减弱血管紧张素II诱导的Ins(1,4,5)P3生成;然而,仅在血管紧张素II剂量为10^(-10) M时,钙离子信号才受到抑制。在分离肝细胞前72小时用百日咳毒素处理大鼠,可阻断EGF增加Ins(1,4,5)P3和Ins(1,3,4)P3的能力,但不抑制任何浓度血管紧张素II刺激InsP3或肌醇四磷酸生成的能力。百日咳毒素选择性消除EGF刺激的肌醇磷脂分解这一观察结果表明,EGF和血管紧张素II在肝细胞中激活磷脂酶C的机制不同。

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