論文

査読有り
2012年3月

Impregnation of plasmid DNA into three-dimensional PLGA scaffold enhances DNA expression of mesenchymal stem cells in vitro

PHARMAZIE
  • Pei-Hong Miao
  • ,
  • Cai-Xia He
  • ,
  • Yu-Lan Hu
  • ,
  • Yasuhiko Tabata
  • ,
  • Jian-Qing Gao
  • ,
  • Zhong-Jie Hu

67
3
開始ページ
229
終了ページ
232
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1691/ph.2012.1077
出版者・発行元
GOVI-VERLAG PHARMAZEUTISCHER VERLAG GMBH

Current efforts had been made to undertake a three-dimensional (3-D) reverse transfection of bone marrow-derived mesenchymal stem cells (BM-MSCs) in PLGA scaffolds. As a kind of multipotent stem cells, BM-MSCs show great potential and tremendous capacity in the gene transfection field and PLGA 3-D scaffold has been shown to be a biomaterial that provides structural support to cells proliferation and tissue engineering. The objective of this study was to assess the transfection efficiency of BM-MSCs with a 3-D reverse transfection method by using PLGA scaffold and observe the SEM photographs of BM-MSCs cultured on PLGA scaffold. BM-MSCs were cultured in 3-D PLGA scaffold which was incorporated with pullulan-spermine/pGL3. It was shown that the gene expression duration of BM-MSCs transfected using 3D reverse method with pullulan-spermine/DNA in the presence of serum maintained 12 days at high levels as compared with the plasmid DNA in medium, and scanning electronic microscopy (SEM) photographs of BM-MSCs cultured on PLGA scaffold exhibited robust cell attachment and viability when cultured in PLGA scaffold in vitro. This study demonstrates that the 3-D reverse transfection method of BM-MSCs using PLGA scaffold could achieve long gene expression in a relatively high level, therefore this transfection system is promising in gene transfection and tissue engineering.

リンク情報
DOI
https://doi.org/10.1691/ph.2012.1077
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000303182300006&DestApp=WOS_CPL
ID情報
  • DOI : 10.1691/ph.2012.1077
  • ISSN : 0031-7144
  • Web of Science ID : WOS:000303182300006

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