The Klotho gene family as a regulator of endocrine fibroblast growth factors

被引:148
作者
Kurosu, Hiroshi [1 ]
Kuro-o, Makoto [2 ]
机构
[1] Tokyo Womens Med Univ, Dept Hyg & Publ Hlth 1, Shinjuku Ku, Tokyo 1628666, Japan
[2] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
关键词
Klotho; beta Klotho; FGF15; FGF19; FGF21; FGF23; Metabolism; VITAMIN-D-RECEPTOR; BILE-ACID SYNTHESIS; FGF RECEPTOR; MICE LACKING; BETA-KLOTHO; PPAR-ALPHA; OSTEOCLAST DIFFERENTIATION; FUNCTIONAL VARIANT; METABOLIC-ACTIVITY; STRUCTURAL BASIS;
D O I
10.1016/j.mce.2008.10.052
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Klotho gene encodes a single-pass transmembrane protein and functions as an aging-suppressor gene, which extends lifespan when overexpressed and accelerates the development of aging-like phenotypes when disrupted in mice. Fibroblast growth factor 23 (FGF23) is a bone-derived hormone that regulates phosphate and vitamin D homeostasis. It has been shown that Klotho-deficient mice and Fgf23 knockout mice exhibit identical phenotypes. This observation led to the identification of Klotho as a cofactor essential for interactions between FGF23 and FCF receptors. In addition to the Klotho-FGF23 axis, recent studies has shown that beta Klotho, a Klotho family protein, also functions as a cofactor required for FGF19 and FGF21 signaling and determines the tissue-specific metabolic activities of FGF19 and FGF21. This review summarizes recent progress in understanding of Klotho and beta Klotho function in the regulation of tissue-specific metabolic activity of the endocrine fibroblast growth factors (FGF19, FGF21, and FGF23). (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:72 / 78
页数:7
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