Prostaglandin E2 (PGE2), a bone-resorption factor, was essentially the sole arachidonate metabolite in an osteoblastic cell line cloned from mouse calvaria (MC3T3-E1). When the cells were cultured in the presence of 2% newborn bovine serum, 1 microM epinephrine markedly stimulated PGE2 synthesis from endogenous arachidonic acid. The PGE2 synthesis commenced after a lag phase of 1-2 h, and reached a maximum at about 3 h after the addition of epinephrine. The effect of epinephrine was inhibited by propranolol, and epinephrine could be replaced by isoproterenol, suggesting beta-adrenergic stimulation of PGE2 production. A rapid increase in intracellular cAMP was observed upon the addition of epinephrine. When the intracellular cAMP level was raised using cholera toxin or forskolin, the PGE2 synthesis was also stimulated. The enhanced PGE2 synthesis was attributed to an increased level of cyclooxygenase, which was shown by immunoprecipitation of the enzyme using anti-cyclooxygenase antibody. Inhibitors of transcription and translation suppressed the epinephrine-dependent increase in cyclooxygenase activity. These findings suggest induction of cyclooxygenase involving cAMP via an as yet unclarified mechanism.

译文

前列腺素E2 (PGE2) 是一种骨吸收因子,本质上是从小鼠颅骨 (MC3T3-E1) 克隆的成骨细胞系中唯一的花生四烯酸代谢物。当在2% 新生牛血清存在下培养细胞时,1微米肾上腺素显著刺激内源性花生四烯酸合成PGE2。PGE2合成在1-2小时的滞后阶段开始,并在添加肾上腺素后约3小时达到最大值。肾上腺素的作用被普萘洛尔抑制,肾上腺素可以被异丙肾上腺素代替,表明 β-肾上腺素能刺激PGE2的产生。添加肾上腺素后,观察到细胞内cAMP迅速增加。当使用霍乱毒素或福司可林提高细胞内cAMP水平时,也刺激了PGE2的合成。PGE2合成的增强归因于环氧合酶水平的升高,这通过使用抗环氧合酶抗体对酶进行免疫沉淀来证明。转录和翻译抑制剂抑制了肾上腺素依赖性环氧合酶活性的增加。这些发现表明,通过尚未阐明的机制诱导涉及cAMP的环氧合酶。

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