Tissue-specific Expression of βKlotho and Fibroblast Growth Factor (FGF) Receptor Isoforms Determines Metabolic Activity of FGF19 and FGF21
The University of Texas Southwestern Medical Center · New York University
Abstract
The fibroblast growth factor (FGF) 19 subfamily of ligands, FGF19, FGF21, and FGF23, function as hormones that regulate bile acid, fatty acid, glucose, and phosphate metabolism in target organs through activating FGF receptors (FGFR1–4). We demonstrated that Klotho and βKlotho, homologous single-pass transmembrane proteins that bind to FGFRs, are required for metabolic activity of FGF23 and FGF21, respectively. Here we show that, like FGF21, FGF19 also requires βKlotho. Both FGF19 and FGF21 can signal through FGFR1–3 bound by βKlotho and increase glucose uptake in adipocytes expressing FGFR1. Additionally, both FGF19 and FGF21 bind to the βKlotho-FGFR4 complex; however, only FGF19 signals efficiently through…
Citation impact
- FWCI
- 11.03
- Percentile
- 100%
- References
- 36
Authors
10- HKHiroshi Kurosu
The University of Texas Southwestern Medical Center
- MCMihwa Choi
The University of Texas Southwestern Medical Center
- YOYasushi Ogawa
The University of Texas Southwestern Medical Center
- ASAddie Smith Dickson
The University of Texas Southwestern Medical Center
- RGRegina Goetz
New York University
Topics & keywords
- FGF19
- FGF21
- Fibroblast growth factor receptor 4
- Fibroblast growth factor
- Klotho
- Fibroblast growth factor receptor
- Fibroblast growth factor receptor 1
- Biology