Department of Pharmacology Medical Biological Laboratory T.N.O. P.O. Box 45 Rijswijk 2280 AA The Netherlands.
Mediators Inflamm. 1992;1(6):385-90. doi: 10.1155/S0962935192000589.
Proliferating keratinocyte cultures have been reported to synthesize higher concentrations of prostaglandin (PG) E than confluent ones. As interleukin-1 (IL-1) stimulates keratinocyte PGE synthesis we investigated whether the degree of confluency of the keratinocyte culture modified the response of the cells to IL-1. It was found that IL-1alpha (100 U/ml) stimulated PGE(2) synthesis by proliferating (7 days in culture) but not differentiating (14 days in culture) keratinocytes. Similar effects were observed using tumour necrosis factor-alpha. Both arachidonic acid (AA) and the calcium ionophore A23187 stimulated PGE(2) synthesis by 7 and 14 day cultures although the increase was greatest when 7 day cultures were used. Our data indicate that there is a specific down-regulation of the mechanism(s) by which some inflammatory cytokines stimulate keratinocyte eicosanoid synthesis as cultured keratinocytes begin to differentiate.
增殖的角质形成细胞培养物已被报道比汇合的角质形成细胞培养物合成更高浓度的前列腺素 (PG) E。由于白细胞介素-1 (IL-1) 刺激角质形成细胞 PGE 合成,我们研究了角质形成细胞培养物的汇合程度是否改变了细胞对 IL-1 的反应。结果发现,IL-1alpha(100 U/ml)刺激增殖(培养 7 天)但不分化(培养 14 天)的角质形成细胞合成 PGE(2)。使用肿瘤坏死因子-α也观察到类似的效果。花生四烯酸 (AA) 和钙离子载体 A23187 均刺激 7 天和 14 天培养物合成 PGE(2),尽管当使用 7 天培养物时增加最大。我们的数据表明,随着培养的角质形成细胞开始分化,一些炎症细胞因子刺激角质形成细胞类二十烷酸合成的机制受到特异性下调。