Thomassen, Martin;
Rose, Adam J.;
Jensen, Thomas E.;
Maarbjerg, Stine J.;
Bune, Laurids;
Leitges, Michael;
Richter, Erik A.;
Bangsbo, Jens;
Nordsborg, Nikolai B.
Protein kinase Cα activity is important for contraction-induced FXYD1 phosphorylation in skeletal muscle
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Media type:
E-Article
Title:
Protein kinase Cα activity is important for contraction-induced FXYD1 phosphorylation in skeletal muscle
Contributor:
Thomassen, Martin;
Rose, Adam J.;
Jensen, Thomas E.;
Maarbjerg, Stine J.;
Bune, Laurids;
Leitges, Michael;
Richter, Erik A.;
Bangsbo, Jens;
Nordsborg, Nikolai B.
imprint:
American Physiological Society, 2011
Published in:American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Description:
<jats:p>Exercise-induced phosphorylation of FXYD1 is a potential important regulator of Na<jats:sup>+</jats:sup>-K<jats:sup>+</jats:sup>-pump activity. It was investigated whether skeletal muscle contractions induce phosphorylation of FXYD1 and whether protein kinase Cα (PKCα) activity is a prerequisite for this possible mechanism. In part 1, human muscle biopsies were obtained at rest, after 30 s of high-intensity exercise (166 ± 31% of V̇o<jats:sub>2max</jats:sub>) and after a subsequent 20 min of moderate-intensity exercise (79 ± 8% of V̇o<jats:sub>2max</jats:sub>). In general, FXYD1 phosphorylation was increased compared with rest both after 30 s ( P < 0.05) and 20 min ( P < 0.001), and more so after 20 min compared with 30 s ( P < 0.05). Specifically, FXYD1 ser63, ser68, and combined ser68 and thr69 phosphorylation were 26–45% higher ( P < 0.05) after 20 min of exercise than at rest. In part 2, FXYD1 phosphorylation was investigated in electrically stimulated soleus and EDL muscles from PKCα knockout (KO) and wild-type (WT) mice. Contractile activity caused FXYD1 ser68 phosphorylation to be increased ( P < 0.001) in WT soleus muscles but to be reduced ( P < 0.001) in WT extensor digitorum longus. In contrast, contractile activity did not affect FXYD1 ser68 phosphorylation in the KO mice. In conclusion, exercise induces FXYD1 phosphorylation at multiple sites in human skeletal muscle. In mouse muscles, contraction-induced changes in FXYD1 ser68 phosphorylation are fiber-type specific and dependent on PKCα activity.</jats:p>