Department of Orthodontics and Oral Biology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Med Sci Sports Exerc. 2010 Apr;42(4):813-9. doi: 10.1249/MSS.0b013e3181beeb52.
The purpose of this study was to establish an in vivo model for muscle regeneration after strain injury in the presence of a fibrotic discontinuity.
The musculus soleus of 5-wk-old male rats was exposed, completely lacerated, and sutured together with or without a collagen scaffold in between the muscle ends. The scaffold represents a fibrotic discontinuity in the muscle. Muscle healing was evaluated after 14 d by general histology and staining for myofibroblasts, satellite cells (activated), and inflammatory cells.
Around all wounds, satellite cells were activated. Inside the collagen scaffolds, satellite cells were absent, indicating that muscle regeneration was impaired. In the wounds without a collagen scaffold, the lacerated and the sutured myofibers contacted and had already started to regenerate, whereas this did not occur with an implanted scaffold.
A fibrotic discontinuity, such as an implanted collagen scaffold, delays muscle regeneration in skeletal muscle. This model is suitable to study skeletal muscle regeneration in the presence of a fibrotic lesion and to evaluate new treatment modalities for muscle strain injuries.
本研究旨在建立一种在存在纤维性不连续性的情况下,因应变伤后肌肉再生的体内模型。
暴露 5 周龄雄性大鼠的比目鱼肌,将其完全切开,然后将肌肉两端缝合在一起,中间夹有或不夹胶原支架。支架代表肌肉中的纤维性不连续性。通过一般组织学和肌成纤维细胞、卫星细胞(激活)和炎症细胞的染色,在 14 天后评估肌肉愈合情况。
在所有伤口周围,卫星细胞均被激活。在胶原支架内,卫星细胞缺失,表明肌肉再生受损。在没有胶原支架的伤口中,切开和缝合的肌纤维接触并已开始再生,而植入支架则没有发生这种情况。
纤维性不连续性,如植入的胶原支架,会延迟骨骼肌的再生。该模型适用于研究纤维性病变存在下的骨骼肌再生,并评估肌肉应变损伤的新治疗方法。