Physiological Functions and Regulation of the Na+/H+ Exchanger [NHE1] in Renal Tubule Epithelial Cells

被引:40
作者
Valles, Patricia G. [1 ,2 ]
Bocanegra, Victoria [2 ]
Gil Lorenzo, Andrea [2 ]
Victoria Costantino, Valeria [2 ]
机构
[1] Univ Nacl Cuyo, Area Fisiol Patol, Dept Patol, Fac Ciencias Med, RA-5500 Mendoza, Argentina
[2] Natl Council Sci & Tech Res Argentina, IMBECU CONICET, Lab Fisiol Fisiopatol Renal, Mendoza, Argentina
关键词
NHE1; Programmed cell death; Renal epithelial cells; Intracellular pH; Signaling pathways; Mechanical stretch; THICK ASCENDING LIMB; NA-H EXCHANGE; TRANSEPITHELIAL HCO3-ABSORPTION; GROWTH-FACTOR; MOLECULAR-CLONING; VOLUME REGULATION; APICAL MEMBRANE; PROXIMAL TUBULE; ATP DEPENDENCE; PH REGULATION;
D O I
10.1159/000368521
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The sodium-hydrogen exchanger isoform-1 [NHE1] is a ubiquitously expressed plasma membrane protein that plays a central role in intracellular pH and cell volume homeostasis by catalyzing an electroneutral exchange of extracellular sodium and intracellular hydrogen. Outside of this important physiological function, the NHE1 cytosolic tail domain acts as a molecular scaffold regulating cell survival and actin cytoskeleton organization through NHE1-dependent signaling proteins. NHE1 plays main roles in response to physiological stress conditions which in addition to cell shrinkage and acidification, include hypoxia and mechanical stimuli, such as cell stretch. NHE1-mediated modulation of programmed cell death results from the exchanger-mediated changes in pHi, cell volume, and/or [Na+] I; and, it has recently become known that regulation of cellular signaling pathways are involved as well. This review focuses on NHE1 functions and regulations. We describe evidence showing how these structural actions integrate with ion translocation in regulating renal tubule epithelial cell survival. Copyright (C) 2015 S. Karger AG, Basel
引用
收藏
页码:452 / 466
页数:15
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