Update on FGF23 and Klotho signaling

被引：88

作者：

Erben, Reinhold G. ^{[1
]}

机构：

[1] Univ Vet Med Vienna, Vet Pl 1, A-1210 Vienna, Austria

来源：

MOLECULAR AND CELLULAR ENDOCRINOLOGY | 2016年 / 432卷 / 0C期

基金：

奥地利科学基金会;

关键词：

FGF23; Fibroblast growth factor-23; Klotho; Bone; Kidney; Parathyroid gland; FIBROBLAST-GROWTH-FACTOR; CHRONIC KIDNEY-DISEASE; RENAL PHOSPHATE-TRANSPORT; VITAMIN-D METABOLISM; TRANSCRIPTS ENCODING MEMBRANE; LEFT-VENTRICULAR HYPERTROPHY; FAMILIAL TUMORAL CALCINOSIS; PARATHYROID-HORMONE; HYPOPHOSPHATEMIC RICKETS; IN-VIVO;

D O I：

10.1016/j.mce.2016.05.008

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Fibroblast growth factor-23 (FGF23) is a bone-derived hormone known to suppress phosphate reabsorption and vitamin D hormone production in the kidney. Klotho was originally discovered as an anti aging factor, but the functional role of Klotho is still a controversial issue. Three major functions have been proposed, a hormonal function of soluble Klotho, an enzymatic function as glycosidase, and the function as an obligatory co-receptor for FGF23 signaling. The purpose of this review is to highlight the recent advances in the area of FGF23 and Klotho signaling in the kidney, in the parathyroid gland, in the cardiovascular system, in bone, and in the central nervous system. During recent years, major new functions of FGF23 and Klotho have been discovered in these organ systems. Based on these novel findings, FGF23 has emerged as a pleiotropic endocrine and auto-/paracrine factor influencing not only mineral metabolism but also cardiovascular function. (C) 2016 The Author. Published by Elsevier Ireland Ltd.

引用

页码：66 / 75

页数：10

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