Receptor Specificity of the Fibroblast Growth Factor Family
Open accessAbstract
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.
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FGFR3 and its ligands FGF20 and FGF23 were concomitantly enriched in eGFP+ Paneth-like cells, accompanied by elevated p-FGFR3 levels.
“We then assessed the expression of known FGFR3 ligands56,57 and found concomitant enrichment of FGFR3 and its ligands FGF20 and FGF23 in eGFP+ Paneth-like cells, accompanied by elevated p-FGFR3 levels (Figures 5D, S6D, and S6E).”
From Paneth-like transition drives resistance to dual targeting of KRAS and EGFR in colorectal cancer (2026) · cites this paper as [56]
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References 112 · Cited by 1,164
- Authors
- Zhang, X., Ibrahimi, O. A., Olsen, S. K., Umemori, H., Mohammadi, M., & Ornitz, D. M.
- Affiliations
- Washington University in St. Louis (US)
- New York University (US)
- University of Michigan (US)
- Corresponding author
- Ornitz, David M.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2006-06
- Volume
- 281
- Issue
- 23
- Pages
- 15694-15700
- ISSN
- 0021-9258 (ISSN-L)
- PMC
- PMC2080618
- OpenAlex
- W2055172928
- Cited by
- 1,164
- References
- 112
- Citations by year
- 2026: 21 · 2025: 45 · 2024: 60 · 2023: 60 · 2022: 45 · 2021: 51 · 2020: 62 · 2019: 74 · 2018: 52 · 2017: 59 · 2016: 74 · 2015: 64 · 2014: 66 · 2013: 72 · 2012: 78
- FWCI
- 22.18
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (R01HL076664, HL076664)
- National Institute of Neurological Disorders and Stroke (R01NS065761)
- National Institute of Dental and Craniofacial Research (R01DE013686, DE013686)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fibroblast Growth Factor Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Connective Tissue Growth Factor Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- fibroblast growth factor, fibroblast growth factor receptor, receptor specificity, ligand-receptor pairs, mitogenic activity, heparan sulfate proteoglycans, FGF signaling
- MeSH terms
- Base Sequence, Cell Line, Fibroblast Growth Factors, Humans, Recombinant Proteins, Receptors, Fibroblast Growth Factor, DNA Primers, Reverse Transcriptase Polymerase Chain Reaction
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