• DocumentCode
    2517885
  • Title

    Regeneration of Smooth Muscle Cells from Bone Marrow - Use of Mesenchymal Stem Cells for Tissue Engineering and Cellular Therapeutics

  • Author

    Wang, Nan ; Ma, Linlin ; Zhou, Zhen ; Zhang, Junyun ; Luo, Xuegang ; Jiang, Yong ; Zhang, Tongcun

  • Author_Institution
    Key Lab. of Ind. Microbiol., Tianjin Univ. of Sci. & Technol., Tianjin, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Bone marrow mesenchymal stem cells (MSCs) can differentiate into smooth muscle cells (SMCs) and have tremendous potential for cell therapy and tissue engineering. In this study, to understand the effects of TGF-beta3 on rat bone marrow-derived MSCs and the underlying molecular mechanism of this differentiation process, we investigated that the changes of myocardin-related transcription factors (MRTFs) at the transcriptional level after rat MSCs were treated with TGF-beta3. The results showed that TGF-beta3 increased the expression of contractile genes, such as SM22, smooth muscle-myosin heavy chain (SM-MHC), SM-alpha-actin in MSCs. When TGF-beta3 induced MSCs differentiation into SMCs, myocardin and MRTF-A were activated. The data indicated that TGF-betai3 induced rat bone marrow-derived MSCs differentiation into SMCs by activating mypcardin and MRTF-A.
  • Keywords
    bone; cellular biophysics; genetics; muscle; orthopaedics; patient treatment; proteins; tissue engineering; SM-alpha-actin gene; TGF-beta3 effect; bone marrow; bone marrow-derived MSC; cellular therapy; mesenchymal stem cell; molecular mechanism; myocardin-related transcription factor; smooth muscle cell regeneration; tissue engineering; Biotechnology; Bones; Heart; In vivo; Muscles; Proteins; Regeneration engineering; Sliding mode control; Stem cells; Tissue engineering;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5163291
  • Filename
    5163291