scholarly journals The Effect of Muscle-Regulatory Factor Genes and Satellite Cell Response to Recombinant Hsp70 Protein on Megalobrama amblycephala Skeletal Muscle

Author(s):  
Kecheng Zhu ◽  
Dianchang Zhang ◽  
Huanling Wang
2014 ◽  
Vol 116 (2) ◽  
pp. 149-155 ◽  
Author(s):  
Masaki Horie ◽  
Mitsuhiro Enomoto ◽  
Manabu Shimoda ◽  
Atsushi Okawa ◽  
Shumpei Miyakawa ◽  
...  

Recently, the use of hyperbaric oxygen (HBO) treatments by elite athletes to accelerate recovery from muscle injuries has become increasingly popular. However, the mechanism of promoting muscle regeneration under HBO conditions has not yet been defined. In this study, we investigated whether HBO treatments promoted muscle regeneration and modulated muscle regulatory factor expression in a rat skeletal muscle injury model. Muscle injury was induced by injecting cardiotoxin (CTX) into the tibialis anterior (TA) muscles. As the HBO treatment, rats were placed in an animal chamber with 100% oxygen under 2.5 atmospheres absolute for 2 h/day, 5 days/wk for 2 wk. We then performed histological analyses, measured the maximum force-producing capacity of the regenerating muscle fibers, and performed quantitative RT-PCR analysis of muscle regulatory factor mRNAs. The cross-sectional areas and maximum force-producing capacity of the regenerating muscle fibers were increased by HBO treatment after injury. The mRNA expression of MyoD, myogenin, and IGF-1 increased significantly in the HBO group at 3 and 5 days after injury. The number of Pax7+/MyoD+, Pax7−/MyoD+, and Pax7+/BrdU+-positive nuclei was increased by HBO treatment. In this study, we demonstrated that HBO treatment accelerated satellite cell proliferation and myofiber maturation in rat muscle that was injured by a CTX injection. These results suggest that HBO treatment accelerates healing and functional recovery after muscle injury.


AGE ◽  
2014 ◽  
Vol 36 (4) ◽  
Author(s):  
Tim Snijders ◽  
Lex B. Verdijk ◽  
Joey S. J. Smeets ◽  
Bryon R. McKay ◽  
Joan M. G. Senden ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (10) ◽  
pp. e109739 ◽  
Author(s):  
Leeann M. Bellamy ◽  
Sophie Joanisse ◽  
Amanda Grubb ◽  
Cameron J. Mitchell ◽  
Bryon R. McKay ◽  
...  

2014 ◽  
Vol 46 ◽  
pp. 640
Author(s):  
Robert D. Hyldahl ◽  
Kailee Jackson ◽  
Logan Groscost ◽  
Tyson Welling ◽  
Allen C. Parcell

Immunobiology ◽  
2014 ◽  
Vol 219 (11) ◽  
pp. 850-858 ◽  
Author(s):  
Nan Chen ◽  
Xiao-Ling Wan ◽  
Chun-Xiao Huang ◽  
Wei-Min Wang ◽  
Hong Liu ◽  
...  

2001 ◽  
Vol 189 (2) ◽  
pp. 189-196 ◽  
Author(s):  
Marie Csete ◽  
Jean Walikonis ◽  
Nicole Slawny ◽  
Yuewang Wei ◽  
Sheryl Korsnes ◽  
...  

Development ◽  
1993 ◽  
Vol 117 (4) ◽  
pp. 1409-1420 ◽  
Author(s):  
R. Moore ◽  
F.S. Walsh

The spatiotemporal distribution of M-cadherin mRNA has been determined by in situ hybridization in the mouse embryo and in adult skeletal muscle following experimental regeneration and denervation. M-cadherin mRNA is highly tissue specific and is found only in developing skeletal muscle. In contrast, N-cadherin mRNA has a broader tissue distribution in the embryo, being found on both neural elements and skeletal and cardiac muscle. M-cadherin is expressed in the myotomes shortly after they form, along with the myogenic regulatory factor myogenin. M-cadherin is expressed in muscles derived from the myotomes and is detected in forelimb bud precursor cells at embryonic day 11.5. In the latter case M-cadherin expression appears co-ordinately with that of myogenin and cardiac alpha-actin. Shortly before birth, M-cadherin expression is down regulated. M-cadherin can, however, be re-expressed following experimental regeneration of skeletal muscle. Here M-cadherin is transiently expressed on regenerating myoblasts but not myotubes. Following muscle denervation no evidence was found for re-expression of M-cadherin under conditions where there was strong expression of the nicotinic acetylcholine receptor on myofibres. The highly specific tissue distribution and unique developmental profile distinguishes M-cadherin from other cadherins and suggests a role in cell surface events during early myogenesis.


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