Co-receptor Requirements for Fibroblast Growth Factor-19 Signaling

• Published in: The Journal of biological chemistry 2007-10, Vol.282 (40), p.29069-29072
• Main Authors: Wu, Xinle, Ge, Hongfei, Gupte, Jamila, Weiszmann, Jennifer, Shimamoto, Grant, Stevens, Jennitte, Hawkins, Nessa, Lemon, Bryan, Shen, Wenyan, Xu, Jing, Veniant, Murielle M., Li, Yue-Sheng, Lindberg, Richard, Chen, Jin-Long, Tian, Hui, Li, Yang
• Format: Article
• Language: English
• Subjects: Cell Line; Culture Media, Conditioned - pharmacology; Endocrine System - metabolism; Fibroblast Growth Factors - metabolism; Fibroblast Growth Factors - physiology; Gene Expression Regulation; Glucuronidase - metabolism; Heparitin Sulfate - metabolism; Humans; Mitogen-Activated Protein Kinase 1 - metabolism; Mitogen-Activated Protein Kinase 3 - metabolism; Phosphorylation; Signal Transduction; Transfection
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.C700130200

FGF19 is a unique member of the fibroblast growth factor (FGF) family of secreted proteins that regulates bile acid homeostasis and metabolic state in an endocrine fashion. Here we investigate the cell surface receptors required for signaling by FGF19. We show that βKlotho, a single-pass transmembrane protein highly expressed in liver and fat, induced ERK1/2 phosphorylation in response to FGF19 treatment and significantly increased the interactions between FGF19 and FGFR4. Interestingly, our results show that αKlotho, another Klotho family protein related to βKlotho, also induced ERK1/2 phosphorylation in response to FGF19 treatment and increased FGF19-FGFR4 interactions in vitro, similar to the effects of βKlotho. In addition, heparin further enhanced the effects of both αKlotho and βKlotho in FGF19 signaling and interaction experiments. These results suggest that a functional FGF19 receptor may consist of FGF receptor (FGFR) and heparan sulfate complexed with either αKlotho or βKlotho.