FGF23 acts directly on renal proximal tubules to induce phosphaturia through activation of the ERK1/2-SGK1 signaling pathway

被引:159
作者
Andrukhova, Olena
Zeitz, Ute
Goetz, Regina [2 ]
Mohammadi, Moosa [2 ]
Lanske, Beate [3 ]
Erben, Reinhold G. [1 ]
机构
[1] Univ Vet Med, Dept Biomed Sci, Inst Physiol Pathophysiol & Biophys, A-1210 Vienna, Austria
[2] NYU, Sch Med, New York, NY USA
[3] Harvard Univ, Sch Dent Med, Boston, MA 02115 USA
基金
奥地利科学基金会;
关键词
Fibroblast growth factor-23; Klotho; Phosphate homeostasis; Kidney; Mice; TRANSPORT; KLOTHO; HYPOPHOSPHATEMIA; RECEPTOR; MICE; CELL;
D O I
10.1016/j.bone.2012.05.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fibroblast growth factor-23 (FGF23) is a bone-derived endocrine regulator of phosphate homeostasis which inhibits renal tubular phosphate reabsorption. Binding of circulating FGF23 to FGF receptors in the cell membrane requires the concurrent presence of the co-receptor alpha Klotho. It is still controversial whether alpha Klotho is expressed in the kidney proximal tubule, the principal site of phosphate reabsorption. Hence, it has remained an enigma as to how FGF23 downregulates renal phosphate reabsorption. Here, we show that renal proximal tubular cells do express the co-receptor alpha Klotho together with cognate FGF receptors, and that FGF23 directly downregulates membrane expression of the sodium-phosphate cotransporter NaPi-2a by serine phosphorylation of the scaffolding protein Na+/H+ exchange regulatory cofactor (NHERF)-1 through ERK1/2 and serum/glucocorticoid-regulated kinase-1 signaling. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:621 / 628
页数:8
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