Molecular Structure and Regulation of Vertebrate Na+/H+ Exchangers
Open Access
- 1 November 1994
- journal article
- Published by The Company of Biologists in Journal of Experimental Biology
- Vol. 196 (1) , 337-345
- https://doi.org/10.1242/jeb.196.1.337
Abstract
Na+/H+ exchangers (NHE), also called antiporters, are vital transmembrane transporters involved in multiple cellular functions including the regulation of intracellular pH, the control of cell volume and transepithelial ion transport. These transporters are highly regulated by a remarkably wide variety of stimuli which can modulate their expression level and activity. Five isoforms of Na+/H+ exchangers have been cloned and characterized to date; they define a new gene family of vertebrate transporters. These isoforms share the same overall structure but exhibit differences with respect to amiloride-sensitivity, cellular localization, kinetic variables, regulation by various stimuli and plasma membrane targeting in polarized epithelial cells. Biochemical techniques and molecular genetics tools provide the means of analyzing these transporters at the molecular level. The purpose of this manuscript is to give an overview of the main features of the Na+/H+ exchangers with emphasis on recent advances in comprehension of the structure–function relationship and regulation mechanisms of the ubiquitous isoform: NHE-1.Keywords
This publication has 26 references indexed in Scilit:
- Na+/H+ exchange and growth factor-induced cytosolic pH changes. Role in cellular proliferationPublished by Elsevier ,2003
- The Na+/H+ Exchanger NHE-1 Possesses N- and O-Linked Glycosylation Restricted to the First N-Terminal Extracellular DomainBiochemistry, 1994
- Structure, function, and regulation of vertebrate Na+/H+ exchangersCurrent Opinion in Nephrology and Hypertension, 1993
- Structure/function studies of the epithelial isoforms of the mammalian Na+/H+ exchanger gene familyThe Journal of Membrane Biology, 1993
- Cloning and expression of a cAMP-activated Na+/H+ exchanger: evidence that the cytoplasmic domain mediates hormonal regulation.Proceedings of the National Academy of Sciences, 1992
- Growth Factors Induce Phosphorylation of the Na + /H + Antiporter, a Glycoprotein of 110 kDScience, 1990
- Effect of cell spreading on cytoplasmic pH in normal and transformed fibroblasts.Proceedings of the National Academy of Sciences, 1989
- Arginine vasopressin enhances pHi regulation in the presence of HCO−3 by stimulating three acid-base transport systemsNature, 1989
- Molecular cloning, primary structure, and expression of the human growth factor-activatable antiporterCell, 1989
- Modifier role of internal H+ in activating the Na+–H+ exchanger in renal microvillus membrane vesiclesNature, 1982