Department of Orthodontics, Shanghai Ninth People's Hospital, School of Stomatology, Shanghai Key Laboratory of Stomatology, Shanghai Jiao Tong University, Shanghai, China.
Department of Pharmacology, School of Medicine, Yale University, New Haven, USA.
Biomed Pharmacother. 2018 Jul;103:240-247. doi: 10.1016/j.biopha.2018.04.026. Epub 2018 Apr 24.
The fibroblast growth factors (FGFs) play a critical role during palatogenesis by mediating a variety of cellular responses. Extensive epidemiological and genetic studies over several decades in humans have revealed members of the FGF family function as candidate genes for syndromic and nonsyndromic cleft lip and cleft palate. The findings that FGFs signaling work delicately in the development of palate have been confirmed in mice carrying targeted mutations. Here we try to review recent progress toward a detailed understanding of FGF signaling including FGF7, FGF8, FGF9, FGF10, FGF18 and their receptors FGFR1, FGFR2 in palate development studies and discuss how they interact with other factors on the basis of animal studies regarding cleft palate.
成纤维细胞生长因子(FGFs)在腭发生过程中通过介导多种细胞反应发挥关键作用。几十年来,人类进行的广泛的流行病学和遗传学研究表明,FGF 家族成员是综合征性和非综合征性唇腭裂的候选基因。在携带靶向突变的小鼠中,证实了 FGF 信号在腭发育中的作用非常精细。在这里,我们试图综述 FGF 信号(包括 FGF7、FGF8、FGF9、FGF10、FGF18 及其受体 FGFR1、FGFR2)在腭发育研究中的最新进展,并讨论它们如何在腭裂动物研究的基础上与其他因素相互作用。