Effects of recombinant gene lentivirus containing LIM mineralization protein-1 on proliferation effect and expression of bone marrow mesenchymal stem cells in rats.
- Author:
Chang-sheng LIANG
;
Chuan XIANG
;
Zeng-yong WEI
;
Hui-ming HOU
;
Ying-ze QIN
;
Xiao-chun WEI
- Publication Type:Journal Article
- MeSH: Adaptor Proteins, Signal Transducing; genetics; metabolism; Animals; Cell Proliferation; Cells, Cultured; Cytoskeletal Proteins; genetics; metabolism; Female; Genetic Therapy; Genetic Vectors; genetics; metabolism; Humans; LIM Domain Proteins; genetics; metabolism; Lentivirus; genetics; metabolism; Male; Mesenchymal Stromal Cells; cytology; metabolism; virology; Osteoporosis; genetics; physiopathology; therapy; Rats; Rats, Sprague-Dawley
- From: China Journal of Orthopaedics and Traumatology 2013;26(12):1023-1027
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo explore method of recombinant gene lentivirus containing LIM mineralization protein-1 (LMP-1) in transfecting bone marrow mesenchymal stem cells (BMSC), and to observe the effect of gene LMP-1 on proliferation effect and expression of BMSC.
METHODSSix clean SD rats aged 4 weeks were selected, bone marrow mesenchymal stem cells were extracted under sterile conditions and cultured to the third generation, then divided into three groups:control group (the third generation of BMSC), lentiviral vector transfection group (PGC-FU-GFP and Polybrene were injected into the third generation of BMSC) and recombinant gene transfection group (PGC-FU-LMP-1-GFP and Polybrene transfection were injected into the third generation of BMSC). After 48 hours' transfection, fluorescent expression were detected under immuno-fluorescence microscopy; lentiviral transfection efficiency were detected by flow cytometry; effect of lentiviral transfection on BMSC were evaluated by MTT; gene expression of transfected cells were determined by Western Blot.
RESULTS1) The third generation of BMSC was cultured successfully,and transfected with MOI:100. After 48 hours, green fluorescent expression were detected and transfection efficiency was 67% under immuno-fluorescence microscopy; 2) Compared to control group, there were no statistical differences between control group and other two groups; 3) Western blot teast showed that 72KDa specific band was observed in recombinant gene transfection group and its size was similar to LMP-1 fusion protein (50 kDa+28 kDa=78 kDa).
CONCLUSIONThere is no effect of recombinant gene lentivirus containing LIM on BMSC, and can effectively influence the expression of LMP-1.