Offermanns S, Schultz G
Institut für Pharmakologie, Freie Universität Berlin, Germany.
FEBS Lett. 1992 Oct 5;310(3):260-4. doi: 10.1016/0014-5793(92)81344-l.
Interferon-gamma (IFN gamma) is a potent immunomodulatory cytokine. However, the early mechanisms which mediate the pleiotropic effects of IFN gamma on different cells are as yet poorly understood. Therefore, we tested the role of tyrosine phosphorylation in signalling induced by IFN gamma. IFN gamma was found to induce rapid tyrosine phosphorylation of several proteins in HL-60 cells. This effect was detectable by 2 min, reached a maximum by about 4-16 min and thereafter declined. Tyrosine phosphorylation was dependent on receptor occupation and was maximally stimulated by 10 ng/ml IFN gamma. Treatment of HL-60 cells with the tyrosine kinase inhibitors, genistein and herbimycin A, inhibited both IFN gamma-stimulated tyrosine phosphorylation and IFN gamma-induced Fc receptor expression. Thus, increased tyrosine phosphorylation appears to be an obligatory early and proximal signal mediating at least some of the later cellular responses induced by IFN gamma in HL-60 cells.
γ干扰素(IFNγ)是一种强效的免疫调节细胞因子。然而,介导IFNγ对不同细胞多效性作用的早期机制目前仍知之甚少。因此,我们测试了酪氨酸磷酸化在IFNγ诱导信号传导中的作用。研究发现,IFNγ可诱导HL-60细胞中几种蛋白质快速发生酪氨酸磷酸化。这种效应在2分钟时即可检测到,约4 - 16分钟时达到最大值,随后下降。酪氨酸磷酸化依赖于受体占据情况,且在10 ng/ml IFNγ刺激下达到最大程度。用酪氨酸激酶抑制剂染料木黄酮和除莠霉素A处理HL-60细胞,可抑制IFNγ刺激的酪氨酸磷酸化以及IFNγ诱导的Fc受体表达。因此,酪氨酸磷酸化增加似乎是介导IFNγ在HL-60细胞中诱导的至少一些后期细胞反应的一个必不可少的早期近端信号。