Bailey J M, Makheja A N, Pash J, Verma M
Biochemistry Department, George Washington University School of Medicine, Washington, D.C. 20037.
Biochem Biophys Res Commun. 1988 Dec 30;157(3):1159-63. doi: 10.1016/s0006-291x(88)80995-1.
Prostacyclin synthesis by cultured vascular smooth muscle cells was inactivated by aspirin. Recovery required serum factors replaceable by EGF plus TGF-beta and was blocked by cycloheximide but not by actinomycin D. Recovery of cyclooxygenase activity was prevented by preincubation with dexamethasone (0.1 to 2 microM), which also suppressed basal enzyme activity by up to 70%. A full length 2.8 Kb cDNA hybridization probe for human cyclooxygenase identified a cyclooxygenase messenger RNA of approximately 2.8 Kb in these cells. Cyclooxygenase mRNA levels were enhanced by EGF/TGF-beta, but suppressed completely by corticosteroids. It is concluded that inhibition of prostanoid synthesis by corticosteroids is mediated by suppressing cyclooxygenase messenger RNA. These observations provide a new molecular mechanism for the anti-inflammatory activity of the corticosteroids.
培养的血管平滑肌细胞合成前列环素的过程被阿司匹林灭活。恢复需要可被表皮生长因子(EGF)加转化生长因子-β(TGF-β)替代的血清因子,且被放线菌酮阻断,但不被放线菌素D阻断。用0.1至2微摩尔的地塞米松预孵育可阻止环氧化酶活性的恢复,地塞米松还可将基础酶活性抑制高达70%。用于人环氧化酶的全长2.8千碱基(Kb)的cDNA杂交探针在这些细胞中鉴定出一条约2.8 Kb的环氧化酶信使核糖核酸(mRNA)。环氧化酶mRNA水平被EGF/TGF-β增强,但被皮质类固醇完全抑制。结论是,皮质类固醇对前列腺素合成的抑制是通过抑制环氧化酶信使核糖核酸介导的。这些观察结果为皮质类固醇的抗炎活性提供了一种新的分子机制。