Cover image of the article: Cloning and transient over-expression of the NRF2 gene in mesenchymal stem cells using adenoviral expression system based on the Gateway technology

Image Credit:J Kermanshah Univ Med Sci

Cloning and transient over-expression of the NRF2 gene in mesenchymal stem cells using adenoviral expression system based on the Gateway technology

Authors

Mohammad Mohammadzadeh1, Mehryar Habibi Roudkenar2,*
1Dept. of Basic Sciences, School of Allied Medical Sciences, Gonabad University of Medical Sciences, Gonabad, Iran
2Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
*Corresponding Author: Corresponding author: Mehryar Habibi Roudkenar, Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran, Tel: +98 21 88601599 Email: roudkenar@ibto.ir

Journal of Kermanshah University of Medical Sciences:Vol. 17, issue 5; e77056
Published online:Aug 29, 2013
Article type:Research Article
Received:Nov 19, 2012
Accepted:Apr 30, 2013
How to Cite:Mohammadzadeh M, Habibi Roudkenar M. Cloning and transient over-expression of the NRF2 gene in mesenchymal stem cells using adenoviral expression system based on the Gateway technology. J Kermanshah Univ Med Sci. 2013;17(5):e77056. doi:

Abstract

Background: Increased mesenchymal stem cells (MSCs) survival after transplantation can improve their therapeutic potential. Therefore, manipulation of the MSCs with cytoprotective genes such as NF-E2 Related Factor-2 (NRF2) is important to improve cell therapy efficiency. The aim of this study was cloning and transient over-expression of the NRF2 gene in MSCs by adenoviral expression system.

Methods: NRF2 was isolated from MSCs and cloned into pENTR/TOPO/D vector by TOPO cloning reaction. NRF2 was translocated from pENTR/TOPO/D vector to adenoviral vector using the Gateway technology. The recombinant adenovirus vector was transformed into 293A cells to package recombinant adenovirus particles. Recombinant adenoviruses harboring NRF2 infected MSCs.

Results: NRF2 was successfully isolated, cloned and its accuracy was confirmed by Deoxyribonucleic acid (DNA) sequencing. NRF2 over-expression was evaluated. This over-expression by adenoviral expression system was transient.

Conclusion: NRF2 over-expression in MSCs with adenoviral expression system could be a valuable device because of its transient expression. Stable over-expression of genes in MSCs could not be permitted.

Highlights

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Copyright

© 2013, Journal of Kermanshah University of Medical Sciences. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

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