Key result
Chronic 1 Hz stimulation for up to 42 days induced coordinated expression of SERCA2a and phospholamban proteins via translational and transcriptional control, respectively.
In a canine model, chronic low-frequency stimulation induces a slow-twitch muscle phenotype via distinct transcriptional and translational regulatory mechanisms for phospholamban and SERCA2.
Answers are grounded in this paper and cite their sources.
Remains preclinical in canine skeletal muscle; leaves open whether coordinated SERCA2a/phospholamban regulation can be targeted in human HF.
Chronic 1 Hz stimulation of the canine latissimus dorsi muscle produced a time-dependent switch from the fast-twitch to the slow-twitch phenotype. This included changes in the proteins of the sarcoplasmic reticulum. After 3 days of muscle stimulation, there was down-regulation of fast-twitch Ca-ATPase (SERCA1a) mRNA and induction of slow-twitch Ca-ATPase (SERCA2a) mRNA; most changes in both mRNAs were nearly complete after 14 days of stimulation. Although the induction of phospholamban mRNA began after 3 days of muscle stimulation, its up-regulation was not completed until the muscle had been stimulated for 42 days. The time course of expression of SERCA2a protein was very different from that of SERCA2a mRNA, suggesting that SERCA2 gene expression is regulated at the translational as well as the transcriptional level. The time course of expression of phospholamban protein closely followed that of phospholamban mRNA, suggesting that this gene is under transcriptional control. Thus coordinated expression of SERCA2a and phospholamban proteins is achieved via translational control of the SERCA2 gene and transcriptional control of the phospholamban gene.
No takes yet. Share an insight, caveat, or question.
Hu et al. (1995) studied Skeletal muscle phenotype switching. Chronic 1 Hz stimulation was evaluated on Expression of SERCA2a and phospholamban mRNAs and proteins. Chronic 1 Hz stimulation for up to 42 days induced coordinated expression of SERCA2a and phospholamban proteins via translational and transcriptional control, respectively.
Synapse has enriched 10 related papers. Consider them for comparative context: