MISC

2009年

Suppression of Carbon Tetrachloride-Induced Liver Fibrosis by Transplantation of a Clonal Mesenchymal Stem Cell Line Derived From Rat Bone Marrow

CELL TRANSPLANTATION
  • Marhaen Hardjo
  • ,
  • Masahiro Miyazaki
  • ,
  • Masakiyo Sakaguchi
  • ,
  • Takuro Masaka
  • ,
  • Sukaeni Ibrahim
  • ,
  • Ken Kataoka
  • ,
  • Narn-ho Huh

18
1
開始ページ
89
終了ページ
99
記述言語
英語
掲載種別
DOI
10.3727/096368909788237140
出版者・発行元
COGNIZANT COMMUNICATION CORP

Transplantation of hepatocytes or bone marrow-derived cells has been shown to ameliorate liver fibrosis in animal models, but no direct comparison of relative efficiency has been made. The aim of this study was to compare the efficiency of a bone marrow-derived clonal mesenchymal stem cell line established by LIS (rBM25/S3) with that of its adipogenic or hepatogenic differentiation derivative for Suppression of rat liver fibrosis. After induction of differentiation of rBM25/S3 cells into adipogenic or hepatogenic cells in Culture, we intrasplenically transplanted the three types of cells into rats (3 x 10(7) cells/rat) before and 4 weeks after initiation of carbon tetrachloride treatment (1 ml/kg body weight twice a week for 8 weeks) to induce liver fibrosis. Undifferentiated rBM25/S3 cells were the most effective for suppression of liver fibrosis, followed by the adipogenic cells and hepatogenic cells. Expression levels of MMP-2 and MMP-9 were also highest in undifferentiated rBM25/S3 cells. These results indicate that bone marrow-derived clonal mesenchymal stem cell lines are useful for further mechanistic studies on cell-mediated suppression of liver fibrosis and that such cell lines will provide information on an appropriate cell source for transplantation therapy for cirrhosis.

リンク情報
DOI
https://doi.org/10.3727/096368909788237140
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000266055100009&DestApp=WOS_CPL
ID情報
  • DOI : 10.3727/096368909788237140
  • ISSN : 0963-6897
  • eISSN : 1555-3892
  • Web of Science ID : WOS:000266055100009

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