Genetically Engineered Mesenchymal Stem Cells Stably Expressing Green Fluorescent Protein

Authors

  • Ali Jahanian Najafabadi Molecular Biology, Pasteur Institute of Iran, Tehran, Iran
  • Amaneh Mohammadi Roushande Department of Anatomy, Faculty of Medicine, Medical University of Tabriz, Tabriz, Iran
  • Mahnaz Aghaipoor Research Center, Iranian Blood Transfusion Organization, Tehran Iran
  • Majid Ebrahimi Research Center, Iranian Blood Transfusion Organization, Tehran Iran
  • Maryam Amani Research Center, Iranian Blood Transfusion Organization, Tehran Iran
  • Mohamad Hosein Mohammadi Research Center, Iranian Blood Transfusion Organization, Tehran Iran
  • Mohammad Salimi Research Center, Iranian Blood Transfusion Organization, Tehran Iran
  • Nasser Amirizadeh Research Center, Iranian Blood Transfusion Organization, Tehran Iran
  • Raheleh Halabian Research Center, Iranian Blood Transfusion Organization, Tehran Iran|Biotechnology Department, Tarbiyat Modares University, Tehran, Iran
Abstract:

Objective(s) Mesenchymal stem cells (MSCs) are nonhematopoietic stromal cells that are capable of differentiating into and contribute to the regeneration of mesenchymal tissues. Human mesenchymal stem cells (hMSCs) are ideal targets in cell transplantation and tissue engineering. Enhanced green fluorescent protein (EGFP) has been an important reporter gene for gene therapy. The aim of this study was establishment of MSCs expressing GFP. Materials and Methods MSCs were isolated and characterized by Immunophenotyping. The pEGFP-N1 plasmid was extracted from previously transformed Escherichia. coli cells and transfected into MSCs using FuGENE HD transfection reagent. Stable cells were established in the presence of geneticin. Expression of GFP was detected by RT- PCR, western blot analysis and immunoflorecent microscope. Results MSCs were successfully isolated and characterized. The MSCs transfected with the pEGFP-N1 plasmid expressed GFP both in mRNA and protein levels while cells transfected with empty vector did not. Conclusion The results suggested that this engineered cell line will be used in the future studies and can easily be traced in vivo.

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Journal title

volume 13  issue 2

pages  24- 30

publication date 2010-04-01

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