Mustn1 ablation in skeletal muscle resulted in a 20-50% decrease in ex vivo skeletal muscle contractions and a persistent increase of Type IIb fibers up to 15-fold compared to wild type mice.
Mustn1 ablation in skeletal muscle satellite cells leads to functional alterations including decreased muscle contractions and a shift in muscle fiber types, suggesting a role in muscle physiology and adaptation.
Abstract Mustn1 , a gene expressed exclusively in the musculoskeletal system, was shown in previous in vitro studies to be a key regulator of myogenic differentiation and myofusion. Other studies also showed Mustn1 expression associated with skeletal muscle development and hypertrophy. However, its specific role in skeletal muscle function remains unclear. This study sought to investigate the effects of Mustn1 in a conditional knockout (KO) mouse model in Pax7 positive skeletal muscle satellite cells. Specifically, we investigated the potential effects of Mustn1 on myogenic gene expression, grip strength, alterations in gait, ex vivo investigations of isolated skeletal muscle isometric contractions, and potential changes in the composition of muscle fiber types. Results indicate that Mustn1 KO mice did not present any substantial phenotypic changes or significant variations in genes related to myogenic differentiation and fusion. However, an approximately 10% decrease in overall grip strength was observed in the 2‐month‐old KO mice in comparison to the control wild type (WT), but this decrease was not significant when normalized by weight. KO mice also generated approximately 8% higher vertical force than WT at 4 months in the hindlimb. Ex vivo experiments revealed decreases in about 20 to 50% in skeletal muscle contractions and about 10%–20% fatigue in soleus of both 2‐ and 4‐month‐old KO mice, respectively. Lastly, immunofluorescent analyses showed a persistent increase of Type IIb fibers up to 15‐fold in the KO mice while Type I fibers decreased about 20% and 30% at both 2 and 4 months, respectively. These findings suggest a potential adaptive or compensatory mechanism following Mustn1 loss, as well as hinting at an association between Mustn1 and muscle fiber typing. Collectively, Mustn1 's complex roles in skeletal muscle physiology requires further research, particularly in terms of understanding the potential role of Mustn1 in muscle repair and regeneration, as well as with influence of exercise. Collectively, these will offer valuable insights into Mustn1 's key biological functions and regulatory pathways.
Kim et al. (Wed,) conducted a other in Mustn1 ablation in skeletal muscle. Mustn1 conditional knockout vs. Wild type (WT) control was evaluated on Myogenic gene expression, grip strength, gait, ex vivo isometric contractions, and muscle fiber type composition. Mustn1 ablation in skeletal muscle resulted in a 20-50% decrease in ex vivo skeletal muscle contractions and a persistent increase of Type IIb fibers up to 15-fold compared to wild type mice.