Neufeld G, Mitchell R, Ponte P, Gospodarowicz D
Cancer Research Institute, University of California Medical Center, San Francisco 94143.
J Cell Biol. 1988 Apr;106(4):1385-94. doi: 10.1083/jcb.106.4.1385.
Growth factor over-production by responsive cells might contribute to their autonomous proliferation as well as their acquisition of a transformed phenotype in culture. Basic fibroblast growth factor (bFGF) has been shown to induce transient changes in cell behavior that resemble those encountered in transformed cells. In addition, several types of human tumor cells have been shown to produce bFGF. To determine directly the role that bFGF might play in the induction of the transformed phenotype, we have introduced a human bFGF cDNA expression vector into baby hamster kidney-derived (BHK-21) fibroblasts. One of the BHK transfectants, termed clone 19, expresses the bFGF mRNA and produces biologically active bFGF that accumulates to a high concentration inside the cells. These properties correlate with the ability of the cells to grow in serum-free medium without the addition of exogenous bFGF. Clone 19 cells also proliferated in soft agar, indicating that constitutive expression of the bFGF gene results in a loss of anchorage-dependent growth.
反应性细胞生长因子过度产生可能有助于其自主增殖以及在培养中获得转化表型。碱性成纤维细胞生长因子(bFGF)已被证明可诱导细胞行为的短暂变化,类似于在转化细胞中观察到的变化。此外,已显示几种类型的人类肿瘤细胞可产生bFGF。为了直接确定bFGF在诱导转化表型中可能发挥的作用,我们将人bFGF cDNA表达载体导入了仓鼠肾来源(BHK-21)的成纤维细胞中。其中一个BHK转染子,称为克隆19,表达bFGF mRNA并产生具有生物活性的bFGF,其在细胞内积累到高浓度。这些特性与细胞在无血清培养基中无需添加外源性bFGF即可生长的能力相关。克隆19细胞也能在软琼脂中增殖,表明bFGF基因的组成型表达导致了锚定依赖性生长的丧失。