White J R, Lee J C
Department of Cellular Biochemistry L101, SmithKline Beecham Pharmaceuticals, King of Prussia, PA 19406.
Agents Actions. 1993;39 Spec No:C73-6. doi: 10.1007/BF01972725.
Several protein kinase inhibitors (PKIs) were investigated for their effects on IL-1 beta, TNF alpha and PMA-induced IL-8 production from human umbilical vein endothelial cells (HUVEC). IL-1 beta (ED50 0.07 ng/ml), TNF alpha (ED50 100 ng/ml) and PMA (ED50 20 ng/ml) induced IL-8 production that could be detected as early as 2 h following stimulation. Staurosporine, a potent but non-specific inhibitor of protein kinases, inhibited PMA-induced (IC50 2 nM) but not IL-1 beta or TNF alpha (IC50 > 200 nM) induced IL-8 production. Neither the cAMP-dependent PKI, KT5720, nor the tyrosine PKIs, genistein, tyrphostin (1-100 microM) or lavendustin A (0.0001-1 microM), inhibited IL-8 production elicited by IL-1 beta. However, the macrolide protein kinase inhibitor geldanamycin (IC50 = 30 nM), but not the closely related analog herbimycin A (5-500 nM), inhibited IL-8 production by 60%. Northern blot analysis of IL-8 mRNA revealed that staurosporine suppressed mRNA increase following stimulation by PMA but not by IL-1. It is proposed that a novel protein kinase susceptible to geldanamycin inhibition may be involved in IL-1-mediated signal transduction.
研究了几种蛋白激酶抑制剂(PKIs)对人脐静脉内皮细胞(HUVEC)中白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNFα)和佛波酯(PMA)诱导的IL-8产生的影响。IL-1β(半数有效剂量[ED50]为0.07 ng/ml)、TNFα(ED50为100 ng/ml)和PMA(ED50为20 ng/ml)诱导的IL-8产生最早可在刺激后2小时检测到。星形孢菌素是一种强效但非特异性的蛋白激酶抑制剂,它抑制PMA诱导的(半数抑制浓度[IC50]为2 nM)IL-8产生,但不抑制IL-1β或TNFα(IC50>200 nM)诱导的IL-8产生。环磷酸腺苷(cAMP)依赖性蛋白激酶抑制剂KT5720以及酪氨酸蛋白激酶抑制剂染料木黄酮、 tyrphostin(1 - 100 μM)或拉文杜斯汀A(0.0001 - 1 μM)均不抑制IL-1β诱导的IL-8产生。然而,大环内酯类蛋白激酶抑制剂格尔德霉素(IC50 = 30 nM)可抑制IL-8产生达60%,而与之密切相关的类似物赫曲霉素A(5 - 500 nM)则无此作用。对IL-8信使核糖核酸(mRNA)的Northern印迹分析显示,星形孢菌素可抑制PMA刺激后mRNA的增加,但不抑制IL-1刺激后的增加。研究表明,一种对格尔德霉素抑制敏感的新型蛋白激酶可能参与IL-1介导的信号转导。