作者: Tetsuya Matsuura , Yong Li , Jean-Paul Giacobino , Freddie H. Fu , Johnny Huard
DOI: 10.1002/JOR.20451
关键词: Myosin 、 Myocyte 、 Cytoplasm 、 Cardiotoxin 、 Wound healing 、 Anatomy 、 Biology 、 Skeletal muscle 、 Blot 、 Regeneration (biology) 、 Cell biology
摘要: We used a mouse model of cardiotoxin injury to examine fiber type conversion during muscle repair. evaluated the soleus muscles 37 wild-type mice at 2, 4, 8, and 12 weeks after injury. also antibodies (fMHC sMHC) against fast slow myosin heavy chain classify myofibers into three categories: fast-, slow-, mixed (hybrid)-type (myofibers expressing both fMHC sMHC). Our results revealed an increase in percentage slow-type decrease fast-type repair process. The hybrid-type increased 2 injury, then gradually decreased over following 6 weeks. Similarly, our analysis centronucleated showed decreases percentages fast- myofibers. investigated relationship between myofiber peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1alpha). expression PGC-1alpha protein, which is expressed nucleus cytoplasm regenerating myofibers, sMHC protein with time injection, but we observed no significant differential fibers PGC-1alpha-positive underwent These suggest that contributes this phenomenon could influence recovery injured muscle.