Overexpression of the Na+/K+ ATPase α2 but not α1 isoform attenuates pathological cardiac hypertrophy and remodeling.

Robert N. Correll, Petra Eder, Adam R. Burr, Sanda Despa, Jennifer Davis, Donald M Bers, Jeffery D. Molkentin

Research output: Chapter in Book/Report/Conference proceedingChapter

35 Citations (Scopus)

Abstract

The Na+ / K+ ATPase (NKA) directly regulates intracellular Na+ levels, which in turn indirectly regulates Ca2+ levels by proximally controlling flux through the Na+ / Ca2+ exchanger (NCX1). Elevated Na+ levels have been reported during heart failure, which permits some degree of reverse-mode Ca2+ entry through NCX1, as well as less efficient Ca2+ clearance. To determine whether maintaining lower intracellular Na+ levels by NKA overexpression in the heart would enhance forward-mode Ca2+ clearance and prevent reverse-mode Ca2+ entry through NCX1 to protect the heart. Cardiac-specific transgenic mice overexpressing either NKA-α1 or NKA-α2 were generated and subjected to pressure overload hypertrophic stimulation. We found that although increased expression of NKA-α1 had no protective effect, overexpression of NKA-α2 significantly decreased cardiac hypertrophy after pressure overload in mice at 2, 10, and 16 weeks of stimulation. Remarkably, total NKA protein expression and activity were not altered in either of these 2 transgenic models because increased expression of one isoform led to a concomitant decrease in the other endogenous isoform. NKA-α2 overexpression but not NKA-α1 led to significantly faster removal of bulk Ca2+ from the cytosol in a manner requiring NCX1 activity. Mechanistically, overexpressed NKA-α2 showed greater affinity for Na+ compared with NKA-α1, leading to more efficient clearance of this ion. Furthermore, overexpression of NKA-α2 but not NKA-α1 was coupled to a decrease in phospholemman expression and phosphorylation, which would favor greater NKA activity, NCX1 activity, and Ca2+ removal. Our results suggest that the protective effect produced by increased expression of NKA-α2 on the heart after pressure overload is due to more efficient Ca2+ clearance because this isoform of NKA preferentially enhances NCX1 activity compared with NKA-α1.

Original languageEnglish (US)
Title of host publicationCirculation research
Pages249-256
Number of pages8
Volume114
Edition2
DOIs
StatePublished - 2014

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Cardiomegaly
Protein Isoforms
sodium-translocating ATPase
Pressure
Cytosol

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Correll, R. N., Eder, P., Burr, A. R., Despa, S., Davis, J., Bers, D. M., & Molkentin, J. D. (2014). Overexpression of the Na+/K+ ATPase α2 but not α1 isoform attenuates pathological cardiac hypertrophy and remodeling. In Circulation research (2 ed., Vol. 114, pp. 249-256) https://doi.org/10.1161/CIRCRESAHA.114.302293

Overexpression of the Na+/K+ ATPase α2 but not α1 isoform attenuates pathological cardiac hypertrophy and remodeling. / Correll, Robert N.; Eder, Petra; Burr, Adam R.; Despa, Sanda; Davis, Jennifer; Bers, Donald M; Molkentin, Jeffery D.

Circulation research. Vol. 114 2. ed. 2014. p. 249-256.

Research output: Chapter in Book/Report/Conference proceedingChapter

Correll, RN, Eder, P, Burr, AR, Despa, S, Davis, J, Bers, DM & Molkentin, JD 2014, Overexpression of the Na+/K+ ATPase α2 but not α1 isoform attenuates pathological cardiac hypertrophy and remodeling. in Circulation research. 2 edn, vol. 114, pp. 249-256. https://doi.org/10.1161/CIRCRESAHA.114.302293
Correll, Robert N. ; Eder, Petra ; Burr, Adam R. ; Despa, Sanda ; Davis, Jennifer ; Bers, Donald M ; Molkentin, Jeffery D. / Overexpression of the Na+/K+ ATPase α2 but not α1 isoform attenuates pathological cardiac hypertrophy and remodeling. Circulation research. Vol. 114 2. ed. 2014. pp. 249-256
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