Physiology and pathophysiology of Na+/H+ exchange and Na+ -K+ -2Cl- cotransport in the heart, brain, and blood
- PMID: 16484438
- DOI: 10.1152/ajpregu.00782.2005
Physiology and pathophysiology of Na+/H+ exchange and Na+ -K+ -2Cl- cotransport in the heart, brain, and blood
Abstract
Maintenance of a stable cell volume and intracellular pH is critical for normal cell function. Arguably, two of the most important ion transporters involved in these processes are the Na+/H+ exchanger isoform 1 (NHE1) and Na+ -K+ -2Cl- cotransporter isoform 1 (NKCC1). Both NHE1 and NKCC1 are stimulated by cell shrinkage and by numerous other stimuli, including a wide range of hormones and growth factors, and for NHE1, intracellular acidification. Both transporters can be important regulators of cell volume, yet their activity also, directly or indirectly, affects the intracellular concentrations of Na+, Ca2+, Cl-, K+, and H+. Conversely, when either transporter responds to a stimulus other than cell shrinkage and when the driving force is directed to promote Na+ entry, one consequence may be cell swelling. Thus stimulation of NHE1 and/or NKCC1 by a deviation from homeostasis of a given parameter may regulate that parameter at the expense of compromising others, a coupling that may contribute to irreversible cell damage in a number of pathophysiological conditions. This review addresses the roles of NHE1 and NKCC1 in the cellular responses to physiological and pathophysiological stress. The aim is to provide a comprehensive overview of the mechanisms and consequences of stress-induced stimulation of these transporters with focus on the heart, brain, and blood. The physiological stressors reviewed are metabolic/exercise stress, osmotic stress, and mechanical stress, conditions in which NHE1 and NKCC1 play important physiological roles. With respect to pathophysiology, the focus is on ischemia and severe hypoxia where the roles of NHE1 and NKCC1 have been widely studied yet remain controversial and incompletely elucidated.
Similar articles
-
NKCC1 and NHE1 are abundantly expressed in the basolateral plasma membrane of secretory coil cells in rat, mouse, and human sweat glands.Am J Physiol Cell Physiol. 2005 Aug;289(2):C333-40. doi: 10.1152/ajpcell.00228.2004. Epub 2005 Apr 20. Am J Physiol Cell Physiol. 2005. PMID: 15843440
-
cAMP inhibition of murine intestinal Na/H exchange requires CFTR-mediated cell shrinkage of villus epithelium.Gastroenterology. 2003 Oct;125(4):1148-63. doi: 10.1016/s0016-5085(03)01212-5. Gastroenterology. 2003. PMID: 14517798
-
Na-K-Cl cotransporter-mediated intracellular Na+ accumulation affects Ca2+ signaling in astrocytes in an in vitro ischemic model.J Neurosci. 2004 Oct 27;24(43):9585-97. doi: 10.1523/JNEUROSCI.2569-04.2004. J Neurosci. 2004. PMID: 15509746 Free PMC article.
-
The role of Na-K-Cl co-transporter in cerebral ischemia.Neurol Res. 2005 Apr;27(3):280-6. doi: 10.1179/016164105X25243. Neurol Res. 2005. PMID: 15845211 Review.
-
The Na-K-Cl Co-transporter in astrocyte swelling.Metab Brain Dis. 2010 Mar;25(1):31-8. doi: 10.1007/s11011-010-9180-3. Epub 2010 Mar 25. Metab Brain Dis. 2010. PMID: 20336356 Review.
Cited by
-
The WNK-SPAK/OSR1 Kinases and the Cation-Chloride Cotransporters as Therapeutic Targets for Neurological Diseases.Aging Dis. 2019 Jun 1;10(3):626-636. doi: 10.14336/AD.2018.0928. eCollection 2019 Jun. Aging Dis. 2019. PMID: 31165006 Free PMC article. Review.
-
Structural and functional analysis of the Na+/H+ exchanger.Biochem J. 2007 Feb 1;401(3):623-33. doi: 10.1042/BJ20061062. Biochem J. 2007. PMID: 17209804 Free PMC article. Review.
-
Molecular Characterization and Expression Analysis of the Na+/H+ Exchanger Gene Family in Capsicum annuum L.Front Genet. 2021 Sep 2;12:680457. doi: 10.3389/fgene.2021.680457. eCollection 2021. Front Genet. 2021. PMID: 34539731 Free PMC article.
-
Engaging neuroscience to advance translational research in brain barrier biology.Nat Rev Neurosci. 2011 Mar;12(3):169-82. doi: 10.1038/nrn2995. Nat Rev Neurosci. 2011. PMID: 21331083 Free PMC article. Review.
-
Multifactorial Effects on Different Types of Brain Cells Contribute to Ammonia Toxicity.Neurochem Res. 2017 Mar;42(3):721-736. doi: 10.1007/s11064-016-1966-1. Epub 2016 Jun 10. Neurochem Res. 2017. PMID: 27286679 Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous