Construction of lentiviral vector containing SOX9 gene and its expression in bone marrow mesenchymal stem cells
To construct the lentiviral vector containing SOX9 gene and to detect its expression in MSCs derived from rabbit bone marrow. Human sox-9 gene coding region fragment was obtained by RT-PCR (reverse transcription-polymerase chain reaction) and then cloned into the plasmid of Pwpxl-MOD2 to form Pwpxl-...
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Veröffentlicht in: | Zhong hua yi xue za zhi 2010-12, Vol.90 (47), p.3376-3380 |
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Sprache: | chi |
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Zusammenfassung: | To construct the lentiviral vector containing SOX9 gene and to detect its expression in MSCs derived from rabbit bone marrow.
Human sox-9 gene coding region fragment was obtained by RT-PCR (reverse transcription-polymerase chain reaction) and then cloned into the plasmid of Pwpxl-MOD2 to form Pwpxl-MOD2/SOX9. Pwpxl-MOD2/SOX9, pRsv-REV, pMDlg-Prre and pMD2G were co-transfected into 293T cells to obtain recombinant virus containing SOX9 gene. Meanwhile, Pwpxl-MOD2, pRsv-REV, pMDlg-pRRE and pMD2G were transfected into another group of 293T cells as a control group packing into blank lentiviral vector. Then the packed lentiviral vector was transfected into MSCs which derived from rabbit bone marrow. The expression of SOX9 was detected by both RT-PCR and Western blot. Identification and proliferation of MSCs was determined by MTT after transfection.
The sequencing and restriction analysis showed that SOX9 gene fragment was correctly connected and cloned into the plasmid Pwpxl-MOD in lentiviral vectors. After trans |
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ISSN: | 0376-2491 |
DOI: | 10.3760/cma.j.issn.0376-2491.2010.47.018 |