Editors' ChoiceGrowth Factors

Fated to Promote FGF23 Signaling

+ See all authors and affiliations

Science's STKE  14 Mar 2006:
Vol. 2006, Issue 326, pp. tw92
DOI: 10.1126/stke.3262006tw92

Klotho, a single-pass transmembrane protein expressed predominantly in kidney that is named for the Fate that spins the thread of life, appears to suppress aging: Klotho overexpression extends the life span in mice, whereas Klotho loss-of-function mutations lead to aging-like phenotypes. Although the Klotho extracellular domain may be shed to act as a humoral factor, the role of the full transmembrane form is unknown. Noting that the phenotypes of mice lacking Klotho resemble those of mice lacking fibroblast growth factor-23 (FGF23), Kurosu et al. investigated possible interactions between Klotho and FGF signaling. Immunoprecipitation analysis revealed that Klotho associated with various FGF receptors (FGFRs) coexpressed in 293 cells stably transfected with Klotho. Although the Klotho extracellular domain did not bind FGF23 directly, Klotho enhanced FGF23 binding. Moreover, Klotho expression increased phosphorylation of FGF receptor substrate-2α and p44/42 mitogen-activated protein kinase (MAPK) in response to treatment with FGF23. Thus, the authors conclude that Klotho acts as a cofactor to promote FGF23 signaling.

H. Kurosu, Y. Ogawa, M. Miyoshi, M. Yamamoto, A. Nandi, K. P. Rosenblatt, M. G. Baum, S. Schiavi, M.-C. Hu, O. W. Moe, M. Kuro-o, Regulation of fibroblast growth factor-23 signaling by Klotho. J. Biol. Chem. 281, 6120-6123 (2006). [Abstract] [Full Text]

Related Content