» Articles » PMID: 21720766

Elevated Expression of Activated Na(+)/H(+) Exchanger Protein Induces Hypertrophy in Isolated Rat Neonatal Ventricular Cardiomyocytes

Overview
Publisher Springer
Specialty Biochemistry
Date 2011 Jul 2
PMID 21720766
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The plasma membrane protein the Na(+)/H(+) exchanger isoform1 (NHE1) has been implicated in various cardiac pathologies including ischemia/reperfusion damage to the myocardium and cardiac hypertrophy. Levels of NHE1 protein and activity are elevated in cardiac disease; however, the mechanism by which these factors contribute to the accompanying hypertrophy in the myocardium is still not clear. To investigate the mechanism of NHE1-induced hypertrophy in the myocardium we constructed two adenoviral vectors expressing either wild type NHE1 protein or a constitutively active NHE1 protein. Infection of neonatal rat ventricular cardiomyocytes (NRVM) resulted in elevated expression of both wild type NHE1 or constitutively active NHE1. Only expression of activated NHE1 protein resulted in an increase in cell size and in an increase in protein synthesis in isolated cardiomyocyte cells. The results demonstrate that expression of activated NHE1 promotes cardiac hypertrophy in isolated cardiac cells and that simple elevation of levels of wild type NHE1 protein does not have a significant hypertrophic effect in NRVM. The results suggest that regulation of NHE1 activity is a critical direct effector of the hypertrophic effect induced in the myocardium by the NHE1 protein.

Citing Articles

The Remaining Conundrum of the Role of the Na/H Exchanger Isoform 1 (NHE1) in Cardiac Physiology and Pathology: Can It Be Rectified?.

Karmazyn M, Pierce G, Fliegel L Rev Cardiovasc Med. 2024; 23(8):284.

PMID: 39076631 PMC: 11266974. DOI: 10.31083/j.rcm2308284.


Amino Acids 785, 787 of the Na/H Exchanger Cytoplasmic Tail Modulate Protein Activity and Tail Conformation.

Li X, Tu T, Quan S, Quintero F, Fahlman R, Fliegel L Int J Mol Sci. 2021; 22(21).

PMID: 34768780 PMC: 8583816. DOI: 10.3390/ijms222111349.


Role of Genetic Mutations of the Na/H Exchanger Isoform 1, in Human Disease and Protein Targeting and Activity.

Fliegel L Mol Cell Biochem. 2020; 476(2):1221-1232.

PMID: 33201382 DOI: 10.1007/s11010-020-03984-4.


Structural and Functional Changes in the Na/H Exchanger Isoform 1, Induced by Erk1/2 Phosphorylation.

Fliegel L Int J Mol Sci. 2019; 20(10).

PMID: 31091671 PMC: 6566726. DOI: 10.3390/ijms20102378.


Na+/H+ exchanger isoform 1-induced osteopontin expression facilitates cardiomyocyte hypertrophy.

Mohamed I, Gadeau A, Fliegel L, Lopaschuk G, Mlih M, Abdulrahman N PLoS One. 2015; 10(4):e0123318.

PMID: 25884410 PMC: 4401699. DOI: 10.1371/journal.pone.0123318.


References
1.
Karmazyn M, Sawyer M, Fliegel L . The Na(+)/H(+) exchanger: a target for cardiac therapeutic intervention. Curr Drug Targets Cardiovasc Haematol Disord. 2005; 5(4):323-35. DOI: 10.2174/1568006054553417. View

2.
Michalak M, Fliegel L, Wlasichuk K . Isolation and characterization of calcium binding glycoproteins of cardiac sarcolemmal vesicles. J Biol Chem. 1990; 265(10):5869-74. View

3.
Chan A, Soltys C, Young M, Proud C, Dyck J . Activation of AMP-activated protein kinase inhibits protein synthesis associated with hypertrophy in the cardiac myocyte. J Biol Chem. 2004; 279(31):32771-9. DOI: 10.1074/jbc.M403528200. View

4.
Chen L, Gan X, Haist J, Feng Q, Lu X, Chakrabarti S . Attenuation of compensatory right ventricular hypertrophy and heart failure following monocrotaline-induced pulmonary vascular injury by the Na+-H+ exchange inhibitor cariporide. J Pharmacol Exp Ther. 2001; 298(2):469-76. View

5.
Malo M, Fliegel L . Physiological role and regulation of the Na+/H+ exchanger. Can J Physiol Pharmacol. 2007; 84(11):1081-95. DOI: 10.1139/y06-065. View