Matthay M A, Thiery J P, Lafont F, Stampfer F, Boyer B
Laboratoire de Physiopathologie du Développement, CNRS URA 1337, Paris, France.
J Cell Sci. 1993 Nov;106 ( Pt 3):869-78. doi: 10.1242/jcs.106.3.869.
The effects of growth factors on epithelial cell motility and dispersion have been examined on an immortalized human mammary epithelial cell line, the 184A1 nontumorigenic cell line. Among all the molecules tested, epidermal growth factor (EGF) and transforming growth factor-alpha (TGF-alpha) were demonstrated to stimulate an increase in mammary epithelial cell motility and wound closure that was associated with a morphological transformation of the cells and was accompanied by modifications in cell-cell and cell-substrate adhesion systems. The EGF-induced increase in cell motility and monolayer wound closure occurred over a 24 hour period and was not dependent on an increase in cell number. The effect of EGF was abolished by inhibiting alpha 2 integrins with specific antibodies, indicating that part of the mechanism for the increase in cell motility and accelerated wound closure depends on alpha 2 integrin functional expression. After 72 hours of exposure to EGF, the EGF-induced alterations in cell morphology, motility and cell adhesion systems underwent a spontaneous reversion that was correlated with a 10-fold reduction in the number of EGF receptors. The ability to regulate the scattering response induced by growth factors might be an important feature distinguishing normal epithelial cells from their tumoral counterparts.
在永生化人乳腺上皮细胞系184A1非致瘤细胞系上研究了生长因子对上皮细胞运动性和分散性的影响。在所有测试的分子中,表皮生长因子(EGF)和转化生长因子-α(TGF-α)被证明可刺激乳腺上皮细胞运动性增加和伤口闭合,这与细胞的形态转变相关,并伴随着细胞间和细胞-基质黏附系统的改变。EGF诱导的细胞运动性增加和单层伤口闭合在24小时内发生,且不依赖于细胞数量的增加。用特异性抗体抑制α2整合素可消除EGF的作用,表明细胞运动性增加和伤口闭合加速的部分机制取决于α2整合素的功能表达。暴露于EGF 72小时后,EGF诱导的细胞形态、运动性和细胞黏附系统的改变发生自发逆转,这与EGF受体数量减少10倍相关。调节生长因子诱导的散射反应的能力可能是区分正常上皮细胞与其肿瘤对应细胞的一个重要特征。