FXYD proteins: novel regulators of Na,K-ATPase

被引:14
作者
Delprat, Benjamin [1 ]
Bibert, Stephanie [1 ]
Geering, Kathi [1 ]
机构
[1] Univ Lausanne, Dept Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
来源
M S-MEDECINE SCIENCES | 2006年 / 22卷 / 6-7期
关键词
D O I
10.1051/medsci/20062267633
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Members of the FXYD protein family are small membrane proteins which are characterized by an FXYD motif, two conserved glycines and a serine residue. FXYD proteins show a tissue-specific distribution. Recent evidence suggests that 6 out of 7 FXYD proteins FXYD1 (phospholemman), FXYD2 (gamma subunit of Na,K-ATPase), FXYD3 (Mat-8) FXYD4 (CHIF), FXYD5 (Ric) and FXYD7 associate with Na K-ATPase and modulate its transport properties e.g. its Na+ and/or its K+ affinity in a distinct way. These results highlight the complex regulation of Na+ and K+ transport which is necessary to ensure proper tissue functions such as renal reabsorption, muscle contractility and neuronal excitability. Moreover, mutation of a conserved glycine residue into an arginine residue in FXYD2 has been linked to cases of human hypomagnesemia indicating that dysregulation of Na,K-ATPase by FXYD proteins may be implicated in pathophysiological states. A better characterization of this novel regulatory mechanism of Na,K-ATPase may help to better understand its role in physiological and pathophysiological conditions.
引用
收藏
页码:633 / 638
页数:6
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