Sex-Specific Effect of CARM1 in Skeletal Muscle Adaptations to Exercise

• Published in: Medicine and science in sports and exercise 2024-03, Vol.56 (3), p.486-498
• Main Authors: Vanlieshout, Tiffany L, Stouth, Derek W, Raziee, Rozhin, Sraka, Anne-Sophie J, Masood, Hooriya A, Ng, Sean Y, Mattina, Stephanie R, Mikhail, Andrew I, Manta, Alexander, Ljubicic, Vladimir
• Format: Article
• Language: English
• Subjects: Animals; Female; Humans; Male; Mice; Mice, Inbred C57BL; Motor Activity - physiology; Muscle, Skeletal - metabolism; Physical Conditioning, Animal - physiology; Protein-Arginine N-Methyltransferases - genetics; Protein-Arginine N-Methyltransferases - metabolism
• ISSN: 1530-0315
• DOI: 10.1249/MSS.0000000000003333

The purpose of this study was to determine how the intersection of coactivator-associated arginine methyltransferase 1 (CARM1) and biological sex affects skeletal muscle adaptations to chronic physical activity. Twelve-week-old female (F) and male (M) wild-type (WT) and CARM1 skeletal muscle-specific knockout (mKO) mice were randomly assigned to sedentary (SED) or voluntary wheel running (VWR) experimental groups. For 8 wk, the animals in the VWR cohort had volitional access to running wheels. Subsequently, we performed whole-body functional tests, and 48 h later muscles were harvested for molecular analysis. Western blotting, enzyme activity assays, as well as confocal and transmission electron microscopy were used to examine skeletal muscle biology. Our data reveal a sex-dependent reduction in VWR volume caused by muscle-specific ablation of CARM1, as F CARM1 mKO mice performed less chronic, volitional exercise than their WT counterparts. Regardless of VWR output, exercise-induced adaptations in physiological function were similar between experimental groups. A broad panel of protein arginine methyltransferase (PRMT) biology measurements, including markers of arginine methyltransferase expression and activity, were unaffected by VWR, except for CARM1 and PRMT7 protein levels, which decreased and increased with VWR, respectively. Changes in myofiber morphology and mitochondrial protein content showed similar trends among animals. However, a closer examination of transmission electron microscopy images revealed contrasting responses to VWR in CARM1 mKO mice compared with WT littermates, particularly in mitochondrial size and fractional area. The present findings demonstrate that CARM1 mKO reduces daily running volume in F mice, as well as exercise-evoked skeletal muscle mitochondrial plasticity, which indicates that this enzyme plays an essential role in sex-dependent differences in exercise performance and mitochondrial health.