Overexpression of the Na+/K+ ATPase α2 but not α1 Isoform Attenuates Pathological Cardiac Hypertrophy and Remodeling
Rationale: 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.
Objective: To determine if 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.
Methods and Results: Cardiac-specific transgenic mice overexpressing either the NKA-α1 or α2 were generated and subjected to pressure overload hypertrophic stimulation. We found that while 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 two transgenic models, as 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. Moreover, 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.
Conclusions: 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.
- Received July 29, 2013.
- Revision received October 28, 2013.
- Accepted November 11, 2013.