Adipose-derived stem-cell treatment of skeletal muscle injury.

نویسندگان

  • Ramon Peçanha
  • Luiza de Lima E Silva Bagno
  • Marcelo Baldanza Ribeiro
  • Anna Beatriz Robottom Ferreira
  • Milton Ozório Moraes
  • Gisele Zapata-Sudo
  • Taís Hanae Kasai-Brunswick
  • Antônio Carlos Campos-de-Carvalho
  • Regina Coeli dos Santos Goldenberg
  • João Pedro Saar Werneck-de-Castro
چکیده

BACKGROUND The aim of the present study was to investigate whether adipose-derived stem cells could contribute to skeletal muscle-healing. METHODS Adipose-derived stem cells of male rats were cultured and injected into the soleus muscles of female rats. Two and four weeks after injections, muscles were tested for tetanic force (50 Hz). Histological analysis was performed to evaluate muscle collagen deposition and the number of centronucleated muscle fibers. In order to track donor cells, chimerism was detected with use of real-time polymerase chain reaction targeting the male sex-determining region Y (SRY) gene. RESULTS Two weeks after cell injection, tetanus strength and the number of centronucleated regenerating myofibers, as well as the number of centronucleated regenerating myofibers, were higher in the treated group than they were in the control group (mean and standard error of the mean, 79.2 ± 5.0% versus 58.3 ± 8.1%, respectively [p < 0.05]; and 145 ± 36 versus 273 ± 18 per 10³ myofibers, respectively [p < 0.05]). However, there were no significant differences at four weeks. Treatment did not decrease collagen deposition. Male gene was not detected in female host tissue at two and four weeks after engraftment by polymerase chain reaction analysis. CONCLUSIONS Adipose-derived stem-cell therapy increased muscle repair and force at two weeks, but not four weeks, after injection, suggesting that adipose-derived stem-cell administration may accelerate muscle repair; however, the rapid disappearance of injected cells suggests a paracrine mechanism of action.

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عنوان ژورنال:
  • The Journal of bone and joint surgery. American volume

دوره 94 7  شماره 

صفحات  -

تاریخ انتشار 2012