Na,K-ATPase activity in mouse muscle is regulated by AMPK and PGC-1a
Research output: Contribution to journal › Journal article › Research › peer-review
Na,K-ATPase activity, which is crucial for skeletal muscle function, undergoes acute and long-term regulation in response to muscle activity. The aim of the present study was to test the hypothesis that AMP kinase (AMPK) and the transcriptional coactivator PGC-1a are underlying factors in long-term regulation of Na,K-ATPase isoform (a,ß and PLM) abundance and Na(+) affinity. Repeated treatment of mice with the AMPK activator AICAR decreased total PLM protein content but increased PLM phosphorylation, whereas the number of a- and ß-subunits remained unchanged. The K (m) for Na(+) stimulation of Na,K-ATPase was reduced (higher affinity) after AICAR treatment. PLM abundance was increased in AMPK kinase-dead mice compared with control mice, but PLM phosphorylation and Na,K-ATPase Na(+) affinity remained unchanged. Na,K-ATPase activity and subunit distribution were also measured in mice with different degrees of PGC-1a expression. Protein abundances of a1 and a2 were reduced in PGC-1a +/- and -/- mice, and the ß(1)/ß(2) ratio was increased with PGC-1a overexpression (TG mice). PLM protein abundance was decreased in TG mice, but phosphorylation status was unchanged. Na,K-ATPase V (max) was decreased in PCG-1a TG and KO mice. Experimentally in vitro induced phosphorylation of PLM increased Na,K-ATPase Na(+) affinity, confirming that PLM phosphorylation is important for Na,K-ATPase function. In conclusion, both AMPK and PGC-1a regulate PLM abundance, AMPK regulates PLM phosphorylation and PGC-1a expression influences Na,K-ATPase a(1) and a(2) content and ß(1)/ß(2) isoform ratio. Phosphorylation of the Na,K-ATPase subunit PLM is an important regulatory mechanism.
|Journal||Journal of Membrane Biology|
|Number of pages||10|
|Publication status||Published - 2011|