Di Francesco P, Liboi E
Department of Experimental Medicine and Biochemical Sciences, 2nd University of Rome, Italy.
Int J Tissue React. 1988;10(5):311-9.
Stimulation of the growth of quiescent fibroblasts by polypeptide growth factors is accompanied by the rapid induction of the c-fos proto-oncogene. To investigate whether there exists a relationship between mitogenic activity and c-fos expression, we analysed cellular responses (DNA synthesis and cell growth) and c-fos gene induction (mRNA and proteins) in a rat embryo fibroblast line (EL2) stimulated with epidermal growth factor (EGF), fibroblast growth factor (FGF), 12-O-tetradodecanoyl phorbol-13-acetate (TPA) and transforming growth factor beta (TGF beta). Our results suggest that the susceptibility of EL2 cells to a growth factor could be predicted as a function of the c-fos expression caused by the same growth factor. These also indicate that the c-fos gene expression may have contributed to moving our cells out of the quiescent state, but it is not the only essential event required to effect EL2 cell growth.
多肽生长因子刺激静止的成纤维细胞生长时,会伴随着原癌基因c-fos的快速诱导。为了研究促有丝分裂活性与c-fos表达之间是否存在关联,我们分析了用表皮生长因子(EGF)、成纤维细胞生长因子(FGF)、12-O-十四烷酰佛波醇-13-乙酸酯(TPA)和转化生长因子β(TGFβ)刺激的大鼠胚胎成纤维细胞系(EL2)中的细胞反应(DNA合成和细胞生长)以及c-fos基因诱导(mRNA和蛋白质)。我们的结果表明,EL2细胞对生长因子的敏感性可以根据同一生长因子引起的c-fos表达来预测。这些结果还表明,c-fos基因表达可能有助于使我们的细胞脱离静止状态,但它不是影响EL2细胞生长所需的唯一关键事件。