期刊
LARYNGOSCOPE
卷 123, 期 11, 页码 2728-2734出版社
WILEY
DOI: 10.1002/lary.24060
关键词
Mesenchymal stem cells; muscle regeneration; induced muscle progenitor cells; posterior cricoarytenoid muscle; vocal fold
资金
- Health Sciences Research Grant from the Ministry of Health, Labor and Welfare of Japan
- National Institute of Biomedical Innovation in Japan
- Grants-in-Aid for Scientific Research [23390060, 23390375, 25670135] Funding Source: KAKEN
Objectives/HypothesisTo investigate the functional efficiency of skeletal muscles regenerated by transplantation of bone marrow-derived stromal cells (BSCs) or induced-muscle progenitor cells (IMCs) as assessed in the canine posterior cricoarytenoid (PCA) muscle injury model. Study DesignProspective animal experiment with control. MethodsWe performed BSC/IMC transplantation into injured canine PCA muscles. We investigated the capability of auto- and allo-BSC/IMC transplantation using a gelatin sponge scaffold to promote functional regeneration of PCA muscles. Transplantation was assessed by fiberscopic analysis of vocal fold movement. We also examined the histologic changes of the transplanted regions. As a control, a gelatin sponge scaffold without additional cells was transplanted into the injured area. ResultsAuto-BSC/IMC transplantation effectively restored vocal fold movement, whereas scaffold alone or allo-BSC/IMC transplantation did not. Histologic examination revealed that (in cases of good recovery) muscle regeneration occurred in the area of cell transplantation, and scar formation without muscle regeneration was observed under control conditions. The dogs with autologous transplantation of BSC had faster functional recovery than did dogs treated with autologous transplantation of IMC. ConclusionsFunctional efficiency was shown in skeletal muscles regenerated using BSCs and IMPs. Motor function recovery was observed using autologous transplantation of BSCs and IMCs. Minimal functional recovery was observed using allogeneic transplantation of these cells. Level of EvidenceNA. Laryngoscope, 123:2728-2734, 2013
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