Differential Interactions of FGFs with Heparan Sulfate Control Gradient Formation and Branching Morphogenesis

被引:143
作者
Makarenkova, Helen P. [1 ,2 ]
Hoffman, Matthew P. [3 ]
Beenken, Andrew [4 ]
Eliseenkova, Anna V. [4 ]
Meech, Robyn [2 ,5 ]
Tsau, Cindy [1 ]
Patel, Vaishali N. [3 ]
Lang, Richard A. [6 ,7 ]
Mohammadi, Moosa [4 ]
机构
[1] Scripps Res Inst, Dept Neurobiol, La Jolla, CA 92037 USA
[2] Inst Neurosci, San Diego, CA 92121 USA
[3] Natl Inst Dent & Craniofacial Res, Lab Cell & Dev Biol, NIH, Bethesda, MD 20892 USA
[4] NYU, Sch Med, Dept Pharmacol, New York, NY 10016 USA
[5] Flinders Univ S Australia, Dept Clin Pharmacol, Bedford Pk, SA 5042, Australia
[6] Childrens Hosp Res Fdn, Visual Syst Grp, Dept Ophthalmol, Cincinnati, OH 45229 USA
[7] Childrens Hosp Res Fdn, Div Dev Biol, Cincinnati, OH 45229 USA
关键词
GROWTH-FACTOR; STRUCTURAL BASIS; CELL-PROLIFERATION; RECEPTOR-BINDING; LACRIMAL GLAND; LUNG; MUTATIONS; DIMER; FIBROBLAST-GROWTH-FACTOR-10; SPECIFICITY;
D O I
10.1126/scisignal.2000304
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
The developmental activities of morphogens depend on the gradients that they form in the extracellular matrix. Here, we show that differences in the binding of fibroblast growth factor 7 (FGF7) and FGF10 to heparan sulfate (HS) underlie the formation of different gradients that dictate distinct activities during branching morphogenesis. Reducing the binding affinity of FGF10 for HS by mutating a single residue in its HS-binding pocket converted FGF10 into a functional mimic of FGF7 with respect to gradient formation and regulation of branching morphogenesis. In particular, the mutant form of FGF10 caused lacrimal and salivary gland epithelium buds to branch rather than to elongate. In contrast, mutations that reduced the affinity of the FGF10 for its receptor affected the extent, but not the nature, of the response. Our data may provide a general model for understanding how binding to HS regulates other morphogenetic gradients.
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页数:10
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