Receptor specificity of the fibroblast growth factor family - The complete mammalian FGF family

被引:973
作者
Zhang, Xiuqin
Ibrahimi, Omar A.
Olsen, Shaun K.
Umemori, Hisashi
Mohammadi, Moosa
Ornitz, David M.
机构
[1] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[2] NYU, Sch Med, Dept Pharmacol, New York, NY 10016 USA
[3] Univ Michigan, Sch Med, Dept Biol Chem, Mol & Behav Neurosci Inst, Ann Arbor, MI 48109 USA
关键词
D O I
10.1074/jbc.M601252200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammals, fibroblast growth factors (FGFs) are encoded by 22 genes. FGFs bind and activate alternatively spliced forms of four tyrosine kinase FGF receptors (FGFRs 1-4). The spatial and temporal expression patterns of FGFs and FGFRs and the ability of specific ligand-receptor pairs to actively signal are important factors regulating FGF activity in a variety of biological processes. FGF signaling activity is regulated by the binding specificity of ligands and receptors and is modulated by extrinsic cofactors such as heparan sulfate proteoglycans. In previous studies, we have engineered BaF3 cell lines to express the seven principal FGFRs and used these cell lines to determine the receptor binding specificity of FGFs 1-9 by using relative mitogenic activity as the readout. Here we have extended these semiquantitative studies to assess the receptor binding specificity of the remaining FGFs 10-23. This study completes the mitogenesis-based comparison of receptor specificity of the entire FGF family under standard conditions and should help in interpreting and predicting in vivo biological activity.
引用
收藏
页码:15694 / 15700
页数:7
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