Ca 2+ storage function is altered in the sarcoplasmic reticulum of skeletal muscle lacking mitsugumin 23.

Mitsugumin 23 (MG23) has been identified as a ball-shaped cation channel in the sarcoplasmic reticulum (SR) but its physiological role remains unclear. This study aimed to examine the contribution of MG23 to Ca 2+ storage function in skeletal muscle by using Mg23 -knockout ( Mg23 -/- ) mice. There was no difference in the isometric specific force of the extensor digitorum longus (EDL) and soleus (SOL) muscles between Mg23 -/- and wild-type (Wt) mice. In Mg23 -/- mice, the calsequestrin 2 content in the EDL muscle and SR Ca 2+ -ATPase 2 content in the SOL were increased. We have examined SR and myofibril functions using mechanically skinned fibers and determined their fiber types based on the response to Sr 2+ , which showed that Mg23 -/- mice, compared with Wt, had: 1 ) elevated total Ca 2+ content in the membranous components including SR, mitochondria, and transverse tubular system referred to as endogenous Ca 2+ content, in both type I and II fibers of the EDL and SOL; 2 ) increased maximal Ca 2+ content in both type I and II fibers of the EDL and SOL; 3 ) decreased SR Ca 2+ leakage in type I fibers of the SOL; and 4 ) enhanced SR Ca 2+ uptake in type I fibers of the SOL, although myofibril function was not different in both type I and II fibers of the SOL and EDL muscles. These results suggest that MG23 decreases SR Ca 2+ storage in both type I and type II fibers, likely due to increased SR Ca 2+ leakage. NEW & NOTEWORTHY The function of calcium storage within sarcoplasmic reticulum (SR) plays a pivotal role in influencing the health and disease states of skeletal muscle. In the present study, we demonstrated that mitsgumin 23, a novel non-selective cation channel, modifies SR Ca 2+ storage in skeletal muscle fibers. These findings provide valuable insights into the physiological regulation of Ca 2+ in skeletal muscle, offering significant potential for uncovering the mechanisms underlying muscle fatigue, muscle adaptation, and muscle diseases.