Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, New York 10016, USA.
Nat Rev Mol Cell Biol. 2013 Mar;14(3):166-80. doi: 10.1038/nrm3528. Epub 2013 Feb 13.
Fibroblast growth factors (FGFs) mediate a broad range of functions in both the developing and adult organism. The accumulated wealth of structural information on the FGF signalling pathway has begun to unveil the underlying molecular mechanisms that modulate this system to generate a myriad of distinct biological outputs in development, tissue homeostasis and metabolism. At the ligand and receptor level, these mechanisms include alternative splicing of the ligand (FGF8 subfamily) and the receptor (FGFR1-FGFR3), ligand homodimerization (FGF9 subfamily), site-specific proteolytic cleavage of the ligand (FGF23), and interaction of the ligand and the receptor with heparan sulphate cofactor and Klotho co-receptor.
成纤维细胞生长因子(FGFs)在发育和成年生物体中介导广泛的功能。关于 FGF 信号通路的结构信息的积累已经开始揭示调节该系统的潜在分子机制,以在发育、组织稳态和代谢中产生无数不同的生物学产物。在配体和受体水平上,这些机制包括配体(FGF8 亚家族)和受体(FGFR1-FGFR3)的选择性剪接、配体同源二聚化(FGF9 亚家族)、配体的特异性蛋白水解切割(FGF23)以及配体和受体与硫酸乙酰肝素共因子和 Klotho 共受体的相互作用。