Author/Authors :
Halabian, Raheleh Research Center - Iranian Blood Transfusion Organization, Tehran - Biotechnology Department - Tarbiyat Modares University, Tehran , Mohammadi, ,Mohamad Hosein Research Center - Iranian Blood Transfusion Organization, Tehran , Salimi, Mohammad Research Center - Iranian Blood Transfusion Organization, Tehran , Amani, Maryam Research Center - Iranian Blood Transfusion Organization, Tehran , Mohammadi Roushande, Amaneh Department of Anatomy - Faculty of Medicine - Medical University of Tabriz , Aghaipoor, Mahnaz Research Center - Iranian Blood Transfusion Organization, Tehran , Amirizadeh, Nasser Research Center - Iranian Blood Transfusion Organization, Tehran , Ebrahimi, Majid Research Center - Iranian Blood Transfusion Organization, Tehran , Jahanian Najafabadi, Ali Molecular Biology - Pasteur Institute of Iran, Tehran , Habibi Roudkenar, Mehryar Research Center - Iranian Blood Transfusion Organization, Tehran
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 RTPCR, 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.
Keywords :
Genetic Engineering , Green Fluorescent Protein , Mesenchymal Stem Cells , Transfection