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表皮生长因子刺激人羊膜细胞中前列腺素E2的产生:特异性和非酯化花生四烯酸依赖性

Epidermal growth factor-stimulated prostaglandin E2 production in human amnion cells: specificity and nonesterified arachidonic acid dependency.

作者信息

Casey M L, Mitchell M D, MacDonald P C

机构信息

Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical School, Dallas 75235-9051.

出版信息

Mol Cell Endocrinol. 1987 Oct;53(3):169-76. doi: 10.1016/0303-7207(87)90171-7.

Abstract

The production of prostaglandin E2 (PGE2) by human amnion cells in primary monolayer culture was stimulated 2- to 150-fold by mouse epidermal growth factor (mEGF). The effect of mEGF on amnion cell PGE2 production was dependent on the time of treatment and the concentration of mEGF used. The rate of PGE2 production by these cells was maximal between 2 and 4 h of treatment with mEGF; thereafter, the rate of production of PGE2 declined. The stimulation of PGE2 production was maximal at concentrations of mEGF of greater than 5 ng/ml. A number of other growth factors, steroid and protein hormones, and various other test agents were ineffective or only minimally in stimulating PGE2 production by amnion cells. The stimulatory effect of mEGF on PGE2 production in these cells was dependent on the presence of serum in the culture medium; alternatively, mEGF was effective in stimulating PGE2 production by amnion cells in serum-free medium that was supplemented with arachidonic acid bound to albumin. Thus, we conclude that the marked stimulation of PGE2 production by amnion cells treated with mEGF is not due to an action of mEGF to stimulate the release of arachidonic acid from cellular glycerophospholipid storage forms; rather, these data are supportive of the conclusion that mEGF-stimulated PGE2 production is dependent on the presence of nonesterified, i.e., free, arachidonic acid in the medium.

摘要

在原代单层培养中,人羊膜细胞产生前列腺素E2(PGE2)的过程受到小鼠表皮生长因子(mEGF)2至150倍的刺激。mEGF对羊膜细胞PGE2产生的影响取决于处理时间和所用mEGF的浓度。在用mEGF处理2至4小时之间,这些细胞产生PGE2的速率最高;此后,PGE2的产生速率下降。当mEGF浓度大于5 ng/ml时,对PGE2产生的刺激作用最大。许多其他生长因子、类固醇和蛋白质激素以及各种其他测试剂对刺激羊膜细胞产生PGE2无效或仅有极小的作用。mEGF对这些细胞中PGE2产生的刺激作用取决于培养基中血清的存在;另外,mEGF在补充了与白蛋白结合的花生四烯酸的无血清培养基中能有效刺激羊膜细胞产生PGE2。因此,我们得出结论,用mEGF处理的羊膜细胞对PGE2产生的显著刺激并非由于mEGF刺激细胞甘油磷脂储存形式释放花生四烯酸的作用;相反,这些数据支持以下结论:mEGF刺激的PGE2产生取决于培养基中未酯化的,即游离的花生四烯酸的存在。

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