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Synergistic Stimulation of Prostaglandin E2 Release by Epidermal Growth Factor and a Tumor Promoter Anthralin from Primary Cultures of Mouse Epidermal Cells

机译:协同刺激的前列腺素E2释放的表皮生长因子和肿瘤启动子蒽醌从小鼠表皮细胞的原代培养。

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References(9) Cited-By(4) The tumor promoter anthralin stimulated prostaglandin E2 (PGE2) and arachidonic acid release from primary cultures of mouse epidermal cells. Epidermal growth factor (EGF) hardly stimulated PGE2 release by itself; however, a combination of anthralin and EGF synergistically stimulated PGE2 release. Neither anthralin, EGF nor EGF plus anthralin affected the incorporation of arachidonic acid into cellular phospholipids at least up to 2 hr after the stimulation by these agents. In the presence of EGF, however, [3H]arachidonic aicd in the medium decreased substantially 4 -8 hr after the addition of this agent, indicating that EGF suppresses [3H]arachidonic acid release and stimulates the incorporation of [3H]arachidonic acid into the cells during this time period. Cellular cyclooxygenase activity was increased by treating the cells either with anthralin or EGF, and it was synergistically increased by EGF plus anthralin. Both cycloheximide and actinomycin D inhibited the increase in cyclooxygenase activity caused by EGF plus anthralin. These results indicate that the synergistic stimulation of PGE2 release caused by EGF plus anthralin is due to a synergistic stimulation of arachidonic acid release (in the early phase of stimulation) and a synergistic increase in cyclooxygenase activity, probably a synergistic induction of cyclooxygenase, by these agents.
机译:参考文献(9)被引用的By(4)肿瘤启动子蒽醌刺激小鼠表皮细胞原代培养物中的前列腺素E2(PGE2)和花生四烯酸释放。表皮生长因子(EGF)本身很难刺激PGE2的释放。然而,蒽林和EGF的组合可协同刺激PGE2释放。在这些试剂刺激后至少2小时内,蒽林,EGF或EGF加蒽林均不影响花生四烯酸掺入细胞磷脂中。然而,在存在EGF的情况下,加入该试剂后,培养基中的[3H]花生四烯酸减少了4 -8小时,这表明EGF抑制了[3H]花生四烯酸的释放并刺激了[3H]花生四烯酸的掺入。在这段时间内的细胞。通过用Anthralin或EGF处理细胞可以增加细胞的环氧合酶活性,而通过EGF和Anthralin可以协同提高细胞的环氧合酶活性。环己酰亚胺和放线菌素D均抑制由EGF加蒽醌引起的环氧合酶活性的增加。这些结果表明,由EGF加蒽醌引起的PGE2释放的协同刺激是由于花生四烯酸释放的协同刺激(在刺激的早期阶段)和环氧合酶活性的协同增加(可能是环氧合酶的协同诱导)引起的。代理商。

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