Sato T, Nakajima H, Fujio K, Mori Y
Department of Biochemistry, School of Pharmacy, Tokyo University of Pharmacy and Life Science, Japan.
Prostaglandins. 1997 May;53(5):355-69. doi: 10.1016/0090-6980(97)00036-1.
We demonstrated the effect of epidermal growth factor (EGF) on the production of PGE2 in human squamous carcinoma A431 cells. The production of PGE2 was increased by stimulating the cells with EGF for 2 h and reached a maximum for 10 h. EGF was also found to augment the release of arachidonic acid (AA) following the increase in phospholipase A2 (PLA2) activity (1.7-fold). The induced PLA2 activity was diminished by 4-bromophenacyl bromide, but not by dithiothreitol, indicating that the EGF-induced release of AA was due to the increase in the activity of cytosolic PLA2 (cPLA2). On the other hand, cyclooxygenase (COX) activity was increased (1.6-fold) within 2 h after the EGF-treatment and the induced activity was inhibited by cycloheximide. In addition, Northern blot analysis showed that the level of COX-2 mRNA was increased by the EGF-treatment, whereas no COX-2 mRNA was detected in the untreated cells, indicating that the EGF-induced COX activity was resulted from the increase in the production of COX-2. These results suggest that EGF augments the production of PGE2 by increasing not only the activity of cPLA2 but also the production of COX-2 in A431 cells.
我们证明了表皮生长因子(EGF)对人鳞状细胞癌A431细胞中前列腺素E2(PGE2)产生的影响。用EGF刺激细胞2小时可使PGE2的产生增加,并在10小时达到最大值。还发现EGF在磷脂酶A2(PLA2)活性增加(1.7倍)后会增强花生四烯酸(AA)的释放。4-溴苯甲酰溴可降低诱导的PLA2活性,但二硫苏糖醇则无此作用,这表明EGF诱导的AA释放是由于胞质型PLA2(cPLA2)活性增加所致。另一方面,EGF处理后2小时内环氧合酶(COX)活性增加(1.6倍),且诱导的活性被环己酰亚胺抑制。此外,Northern印迹分析表明,EGF处理可使COX-2 mRNA水平升高,而未处理的细胞中未检测到COX-2 mRNA,这表明EGF诱导的COX活性是由于COX-2产生增加所致。这些结果表明,EGF不仅通过增加cPLA2的活性,还通过增加A431细胞中COX-2的产生来增强PGE2的产生。