The α1- and α2-isoforms of Na-K-ATPase play different roles in skeletal muscle contractility

Author:

He Suiwen1,Shelly Daniel A.2,Moseley Amy E.1,James Paul F.1,James J. Howard3,Paul Richard J.2,Lingrel Jerry B.1

Affiliation:

1. Department of Molecular Genetics, Biochemistry, and Microbiology and

2. Department of Molecular and Cellular Physiology and

3. Department of Surgery, University of Cincinnati, College of Medicine, Cincinnati, Ohio 45267

Abstract

The Na-K-ATPase, which maintains the Na+ and K+ gradients across the plasma membrane, can play a major role in modulation of skeletal muscle contractility. Although both α1- and α2-isoforms of the Na-K-ATPase are expressed in skeletal muscle, the physiological significance of these isoforms in contractility is not known. Evaluation of the contractile parameters of mouse extensor digitorum longus (EDL) was carried out using gene-targeted mice lacking one copy of either the α1- or α2-isoform gene of the Na-K-ATPase. The EDL muscles from heterozygous mice contain approximately one-half of the α1- or α2-isoform, respectively, which permits differentiation of the functional roles of these isoforms. EDL from the α1 +/− mouse shows lower force compared with wild type, whereas that from the α2 +/− mouse shows greater force. The different functional roles of these two isoforms are further demonstrated because inhibition of the α2-isoform with ouabain increases contractility of α1 +/−EDL. These results demonstrate that the Na-K-ATPase α1- and α2-isoforms may play different roles in skeletal muscle contraction.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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