Colotta F, Lampugnani M G, Polentarutti N, Dejana E, Mantovani A
Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
Biochem Biophys Res Commun. 1988 May 16;152(3):1104-10. doi: 10.1016/s0006-291x(88)80398-x.
In the present study we have evaluated the expression of c-fos protooncogene in normal human endothelial cells (HEC) by Northern blot analysis. HEC do not show neither constitutive nor cycloheximide-induced expression of c-fos protooncogene. When HEC were treated with cytokines known to modulate a number of specialized functions of these cells, we observed that, unlike interferon-gamma, interleukin-1 (IL-1) and tumor necrosis factor (TNF) were able to induce appreciable levels of c-fos in HEC. Both IL-1 alpha and IL-1 beta induced c-fos transcripts in HEC. Maximal levels of c-fos mRNA induced by IL-1 were found after 1 hour of treatment, with undetectable levels at 4 and 7 hours. c-fos induction in HEC by IL-1 and TNF may play a role in the acquisition of functional properties induced in HEC by these cytokines.
在本研究中,我们通过Northern印迹分析评估了原癌基因c-fos在正常人内皮细胞(HEC)中的表达。HEC未显示出c-fos原癌基因的组成型表达,也未显示放线菌酮诱导的表达。当用已知可调节这些细胞多种特殊功能的细胞因子处理HEC时,我们观察到,与干扰素-γ不同,白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)能够在HEC中诱导可观水平的c-fos。IL-1α和IL-1β均能在HEC中诱导c-fos转录本。IL-1诱导的c-fos mRNA在处理1小时后达到最高水平,在4小时和7小时时无法检测到。IL-1和TNF在HEC中诱导c-fos可能在这些细胞因子诱导的HEC功能特性的获得中发挥作用。