Effects of lentiviral vectors on DNA damage of human dermal fibroblasts (HDFs)

Abdian, Narges. and Allahbakhshian-Farsani, Mehdi. and Ghasemi-Dehkordi, Payam. and Mirzaeian, Amin. and Saffari-Chaleshtori, Javad. and Sadeghiani, Marzieh. and Hashemzadeh-Chaleshtori, Morteza. and Yazdanpanahi, Nasrin. (2015) Effects of lentiviral vectors on DNA damage of human dermal fibroblasts (HDFs). Journal of Pure and Applied Microbiology, 9 (1). pp. 307-317.


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In present study we evaluated the DNA damages and cytogenetic stability of transducted and non-transducted human dermal fibroblasts (HDFs) by enhanced green fluorescent protein (eGFP) lentiviral vector using karyotyping, comet assay, and molecular techniques. HDFs were isolated from human foreskin samples and eGFP-expressing lentiviral vector were transfected into HEK-293T cells to produce lentiviruses. Then, HDFs at passage 2 were transducted with concentrated eGFP lentivirus and transducted HDFs were detected by fluorescent microscope. The expression levels of cell cycle genes include two subunits of anaphase promoting complex (APC) in transducted and nontransducted HDFs were measured by quantitative real-time PCR and finally, karyotype test and comet assay was performed to evaluate the DNA damages and cytogenetic stability in both groups. The results of karyotype analysis were not showed any abnormalities in karyotype of transducted HDFs by eGFP in compared to normal cells. The mean values of alkaline comet assay parameters on non-transducted (normal cells), eGFP-transducted group and positive control (H2O2 treatment) were calculated by CaspLab software. The comparison of mean difference of comet assay parameters include tail length, comet length, tail moment, and Olive tail moment by T test between eGFP-transducted HDFs and other groups (positive control and non-transducted HDFs) were statistically significant (p≤0.05). The alkaline comet assay on HDFs in eGFP-transducted group was showed small tail and indicated slight genetic damage compared with non-transducted group. Furthermore, the analysis of real-time PCR on expression of APC2 and APC7 genes in non-transducted HDFs compared with eGFP-transducted HDFs were not significant (p≤0.05). These findings indicated that integration of lentiviral vectors in first passage of transducted HDFs could not disturb the DNA structure and create chromosome instability. So in genetic engineering and gene transformation these vectors in first passages are useful.

Item Type: Article
Additional Information: cited By 0
Uncontrolled Keywords: anaphase promoting complex; enhanced green fluorescent protein; lentivirus vector, Article; cell cycle; chromosomal instability; comet assay; cytogenetics; DNA damage; DNA structure; fluorescence microscopy; gene amplification; gene expression; genetic damage; human; human cell; in vitro study; karyotype; karyotyping; male; newborn; real time polymerase chain reaction; reverse transcription polymerase chain reaction; skin fibroblast; viral gene delivery system, Lentivirus
Subjects: WR Dermatology
QU Biochemistry > Cell biology and genetics
Divisions: Reserach Vice-Chancellar Department > Cellular and Molecular Research Center
Reserach Vice-Chancellar Department > Clinical Biochemistry Research Center
Depositing User: Users 1 not found.
Date Deposited: 30 Jul 2017 03:13
Last Modified: 24 Apr 2018 09:14
URI: http://eprints.skums.ac.ir/id/eprint/2013

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