Tarutani Masahito, Cai Ti, Dajee Maya, Khavari Paul A
Veterans Affairs Valo Alto Healthcare System and the Program in Epithelial Biology, Stanford University School of Medicine, Stanford, California 94305, USA.
Cancer Res. 2003 Jan 15;63(2):319-23.
Ras effects vary with developmental setting, with oncogenic RAS activation implicated in epithelial carcinogenesis. In epidermal cells, previous studies described conflicting Ras impacts on growth and differentiation, with the only in vivo studies relying on constitutive alterations of Ras function throughout development. To study Ras effects in developmentally mature adult epidermis, we expressed a 4-hydroxytamoxifen (4OHT)-regulated Ras fusion in transgenic mice using the keratin 14 promoter. Resulting adult K14-ER:Ras mice displayed 4OHT-inducible activation of Ras as well as elements of Raf/mitogen-activated protein kinase (MAPK) but not RalGDS/Ral or phosphatidylinositol 3'-kinase (PI3K)/Akt downstream Ras effector pathways. Ras reversibly induced massive cutaneous hyperplasia and suppressed differentiation. Ras-driven hyperproliferation was accompanied by increases in beta1 and beta4 integrin epidermal progenitor markers. Epidermal expression of inducible Raf produced similar changes. These findings indicate that activation of Ras in adult epidermis promotes proliferation and inhibits differentiation and that Raf is sufficient to mediate these effects.
Ras的作用因发育环境而异,致癌性RAS激活与上皮细胞癌变有关。在表皮细胞中,先前的研究描述了Ras对生长和分化的影响相互矛盾,仅有的体内研究依赖于整个发育过程中Ras功能的组成性改变。为了研究Ras在发育成熟的成年表皮中的作用,我们使用角蛋白14启动子在转基因小鼠中表达了一种4-羟基他莫昔芬(4OHT)调节的Ras融合蛋白。由此产生的成年K14-ER:Ras小鼠表现出4OHT诱导的Ras激活以及Raf/丝裂原活化蛋白激酶(MAPK)的激活,但不包括RalGDS/Ral或磷脂酰肌醇3'-激酶(PI3K)/Akt下游Ras效应器途径。Ras可逆地诱导大量皮肤增生并抑制分化。Ras驱动的过度增殖伴随着β1和β4整合素表皮祖细胞标志物的增加。诱导型Raf的表皮表达产生了类似的变化。这些发现表明,成年表皮中Ras的激活促进增殖并抑制分化,并且Raf足以介导这些效应。