Study on transfection of dog bone mesenchymal stem cells with BMP-2/VEGF165-based lentivirus vector
Tuo Wang, Renfu Quan, Liang Zhang, Qiang Li, Guoping Cao, Wei Zhuang, Rongxue Shao
Abstract
Tuo Wang, Renfu Quan, Liang Zhang, Qiang Li, Guoping Cao, Wei Zhuang, Rongxue Shao
Abstract
Objective To transfect the dog bone mesenchymal stem cells (BMSCs) with lentivirus-mediated vascular endothelial growth factor 165 (VEGF165) and bone morphogenetic protein 2 (BMP-2) and observe the expressions of VEGF165 and BMP-2 in BMSCs. Methods Lentivirus vectors carrying VEGF165 and BMP-2 genes were constructed and used to transfect dog third-generation BMSCs, including untransfected group, VEGF165 group, BMP-2 group and double-gene (VEGF165+ BMP-2) group. Expressions of VEGF165 and BMP-2 mRNA were detected by RT-PCR 7 d after the transfection.Expressions of VEGF165 and BMP-2 protein were detected by Western blotting 5 d and 28 d after the transfection. Cell growth was detected by MTT assay. Results RT-PCR showed high expression of VEGF165 mRNA in VEGF165 and double-gene groups, and BMP-2 mRNA in BMP-2 and double-gene groups, but there was no significant difference in group comparison(P>0.05). Western blotting showed specific performance of VEGF165 protein in VEGF165 and double-gene groups, and BMP-2 protein in BMP-2 and double-gene groups. In MTT assay cells were found to have 2-3 d relatively stationary phase in the early period, proliferated rapidly at 3 d, reaching the logarithmic growth, and entered the plateau phase with slow propagation. There was no significant difference in absorbance value before and after the transfection (P>0.05). Conclusion BMSCs with highly expressed VEGF165 and BMP-2 can be successfully obtained by lentiviral transduction. Key words: Tissue engineering; Mesenchymal stem cells; Lentivirus; Transfection
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Objective To transfect the dog bone mesenchymal stem cells (BMSCs) with lentivirus-mediated vascular endothelial growth factor 165 (VEGF165) and bone morphogenetic protein 2 (BMP-2) and observe the expressions of VEGF165 and BMP-2 in BMSCs. Methods Lentivirus vectors carrying VEGF165 and BMP-2 genes were constructed and used to transfect dog third-generation BMSCs, including untransfected group, VEGF165 group, BMP-2 group and double-gene (VEGF165+ BMP-2) group. Expressions of VEGF165 and BMP-2 mRNA were detected by RT-PCR 7 d after the transfection.Expressions of VEGF165 and BMP-2 protein were detected by Western blotting 5 d and 28 d after the transfection. Cell growth was detected by MTT assay. Results RT-PCR showed high expression of VEGF165 mRNA in VEGF165 and double-gene groups, and BMP-2 mRNA in BMP-2 and double-gene groups, but there was no significant difference in group comparison(P>0.05). Western blotting showed specific performance of VEGF165 protein in VEGF165 and double-gene groups, and BMP-2 protein in BMP-2 and double-gene groups. In MTT assay cells were found to have 2-3 d relatively stationary phase in the early period, proliferated rapidly at 3 d, reaching the logarithmic growth, and entered the plateau phase with slow propagation. There was no significant difference in absorbance value before and after the transfection (P>0.05). Conclusion BMSCs with highly expressed VEGF165 and BMP-2 can be successfully obtained by lentiviral transduction. Key words: Tissue engineering; Mesenchymal stem cells; Lentivirus; Transfection
Key concepts: Transfection, Molecular biology, Mesenchymal stem cell, Lentivirus, Bone morphogenetic protein 2, Blot, Bone morphogenetic protein, MTT assay