Tichelaar J W, Lu W, Whitsett J A
Children's Hospital Medical Center, Division of Pulmonary Biology, Cincinnati, Ohio 45229-3039, USA.
J Biol Chem. 2000 Apr 21;275(16):11858-64. doi: 10.1074/jbc.275.16.11858.
Effects of fibroblast growth factor-7 (FGF-7) on lung morphogenesis, respiratory epithelial cell differentiation, and proliferation were assessed in transgenic mice in which the human FGF-7 cDNA was controlled by a conditional promoter under the direction of regulatory elements from either the human surfactant protein-C (SP-C) or rat Clara cell secretory protein (ccsp) genes. Expression of FGF-7 was induced in respiratory epithelial cells of the fetal lung by administration of doxycycline to the dam. Prenatally, doxycycline induced FGF-7 mRNA in respiratory epithelial cells in both Sp-c and Ccsp transgenic lines, increasing lung size and causing cystadenomatoid malformation. Postnatally, mice bearing both Ccsp-rtta and (Teto)(7)-cmv-fgf-7 transgenes survived, and lung morphology was normal. Induction of FGF-7 expression by doxycycline in the Ccsp-rtta x (Teto)(7)-cmv-fgf-7 mice caused marked epithelial cell proliferation, adenomatous hyperplasia, and pulmonary infiltration with mononuclear cells. Epithelial cell hyperplasia caused by FGF-7 was largely resolved after removal of doxycycline. Surfactant proteins, TTF-1, and aquaporin 5 expression were conditionally induced by doxycycline. The Sp-c-rtta and Ccsp-rtta activator mice provide models in which expression is conditionally controlled in respiratory epithelial cells in the developing and mature lung, altering lung morphogenesis, differentiation, and proliferation.
在转基因小鼠中评估了成纤维细胞生长因子-7(FGF-7)对肺形态发生、呼吸道上皮细胞分化和增殖的影响。在这些转基因小鼠中,人FGF-7 cDNA由条件启动子控制,该启动子受来自人表面活性蛋白-C(SP-C)基因或大鼠克拉拉细胞分泌蛋白(ccsp)基因的调控元件的指导。通过向母鼠施用强力霉素,在胎儿肺的呼吸道上皮细胞中诱导FGF-7的表达。在产前,强力霉素在Sp-c和Ccsp转基因系的呼吸道上皮细胞中诱导FGF-7 mRNA,增加肺的大小并导致囊性腺瘤样畸形。出生后,同时携带Ccsp-rtta和(Teto)(7)-cmv-fgf-7转基因的小鼠存活下来,并且肺形态正常。在Ccsp-rtta x(Teto)(7)-cmv-fgf-7小鼠中,强力霉素诱导FGF-7表达导致明显的上皮细胞增殖、腺瘤样增生和单核细胞肺浸润。去除强力霉素后,FGF-7引起的上皮细胞增生在很大程度上得到缓解。表面活性蛋白、TTF-1和水通道蛋白5的表达由强力霉素条件性诱导。Sp-c-rtta和Ccsp-rtta激活小鼠提供了模型,其中在发育中和成熟肺的呼吸道上皮细胞中表达受到条件性控制,从而改变肺的形态发生、分化和增殖。