論文

査読有り
2013年11月

Functional Regeneration of Laryngeal Muscle Using Bone Marrow-Derived Stromal Cells

LARYNGOSCOPE
  • Shin-ichi Kanemaru
  • ,
  • Yoshiharu Kitani
  • ,
  • Satoshi Ohno
  • ,
  • Taeko Shigemoto
  • ,
  • Tsuyoshi Kojima
  • ,
  • Seiji Ishikawa
  • ,
  • Masanobu Mizuta
  • ,
  • Shigeru Hirano
  • ,
  • Tatsuo Nakamura
  • ,
  • Mari Dezawa

123
11
開始ページ
2728
終了ページ
2734
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1002/lary.24060
出版者・発行元
WILEY-BLACKWELL

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

リンク情報
DOI
https://doi.org/10.1002/lary.24060
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/23929597
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000326231200037&DestApp=WOS_CPL
ID情報
  • DOI : 10.1002/lary.24060
  • ISSN : 0023-852X
  • eISSN : 1531-4995
  • PubMed ID : 23929597
  • Web of Science ID : WOS:000326231200037

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