首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Time‐coordinated prevalence of extracellular HGF,FGF2 and TGF‐β3 in crush‐injured skeletal muscle
Authors:Mai‐Khoi Q DO  Takahiro SUZUKI  Borjigin GERELT  Yusuke SATO  Wataru MIZUNOYA  Mako NAKAMURA  Yoshihide IKEUCHI  Judy E ANDERSON  Ryuichi TATSUMI
Institution:1. Department of Animal and Marine Bioresource Sciences, Graduate School of Agriculture;2. Faculty of Agriculture, Kyushu University, , Fukuoka, Japan;3. Department of Biological Sciences, Faculty of Science, University of Manitoba, , Winnipeg, Manitoba, Canada
Abstract:Successful regeneration and remodeling of neuromuscular junctions are critical for restoring functional capacities and properties of skeletal muscle after damage, and axon‐guidance molecules may be involved in the signaling that regulates such restoration. Recently, we found that early‐differentiated satellite cells up‐regulate a secreted neural chemorepellent Sema3A upon in vivo muscle‐crush injury. The study also revealed that Sema3A expression is up‐regulated in primary satellite‐cell cultures in response to hepatocyte growth factor (HGF) and basic fibroblast growth factor (FGF2) and is prevented by transforming growth factor (TGF)‐β2, 3. In order to verify the physiological significance of this regulation in vitro, the present study was designed to estimate the time‐course of extracellular HGF, FGF2 and TGF‐β3 concentrations after crush‐injury of Gastrocnemius muscle in the rat lower hind‐limb, using a combination of a non‐homogenization/non‐spin extraction of extracellular wound fluids and enhanced chemiluminescence–Western blotting analyses. Results clearly demonstrated that active HGF and FGF2 are prevalent in 2–8 days post‐crush, whereas active TGF‐β3 increases after 12 days, providing a better understanding of the time‐coordinated levels of HGF, FGF2 and TGF‐β3 that drive regulation of Sema3A expression during regenerative intramuscular moto‐neuritogenesis.
Keywords:crush injury     FGF2     HGF     muscle regeneration     TGF‐β  3
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号