Lü Jining, Izvolsky Konstantin I, Qian Jun, Cardoso Wellington V
Pulmonary Center, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
J Biol Chem. 2005 Feb 11;280(6):4834-41. doi: 10.1074/jbc.M410714200. Epub 2004 Nov 19.
Genetic studies implicate Fgf10-Fgfr2 signaling as a critical regulator of bud morphogenesis in the embryo. However, little is known about the transcriptional targets of Fgf10 during this process. Here we identified global changes in gene expression in lung epithelial explants undergoing FGF10-mediated budding in the absence of other growth factors and mesenchyme. Targets were confirmed by their localization at sites where endogenous Fgf10 signaling is active in embryonic lungs and by demonstrating their induction in intact lungs in response to local application of FGF10 protein. We show that the initial stages of budding are characterized by marked up-regulation of genes associated with cell rearrangement and cell migration, inflammatory process, and lipid metabolism but not cell proliferation. We also found that some genes implicated in tumor invasion and metastatic behavior are epithelial targets of Fgf10 in the lung and other developing organs that depend on Fgf10-Fgfr2 signaling to properly form. Our approach identifies Fgf10 targets that are common to multiple biological processes and provides insights into potential mechanisms by which Fgf signaling regulates epithelial cell behavior.
遗传学研究表明,Fgf10 - Fgfr2信号传导是胚胎中芽形态发生的关键调节因子。然而,在此过程中Fgf10的转录靶点却鲜为人知。在这里,我们确定了在没有其他生长因子和间充质的情况下,经历FGF10介导的出芽过程的肺上皮外植体中基因表达的整体变化。通过它们在内源性Fgf10信号在胚胎肺中活跃的部位的定位,以及通过证明它们在完整肺中对局部应用FGF10蛋白的反应而被诱导,来确认靶点。我们表明,出芽的初始阶段的特征是与细胞重排、细胞迁移、炎症过程和脂质代谢相关的基因显著上调,而不是细胞增殖。我们还发现,一些与肿瘤侵袭和转移行为有关的基因是肺和其他依赖Fgf10 - Fgfr2信号传导正常形成的发育器官中Fgf10的上皮靶点。我们的方法确定了多个生物学过程共有的Fgf10靶点,并深入了解了Fgf信号传导调节上皮细胞行为的潜在机制。