The Osteogenic Study of Tissue Engineering Bone with BMP2 and BMP7 Gene-Modified Rat Adipose-Derived Stem Cell

被引:14
|
作者
Wang Qing [1 ]
Chen Guang-Xing [1 ]
Guo Lin [1 ]
Yang Liu [1 ]
机构
[1] Third Mil Med Univ, Ctr Joint Surg, South West Hosp, Chongqing 400038, Peoples R China
关键词
MARROW STROMAL CELLS; FORMATION IN-VIVO; MORPHOGENETIC PROTEIN-2; LENTIVIRAL VECTOR; EXPRESSION; DEFECTS; VITRO; DIFFERENTIATION; HETERODIMER; TRANSGENE;
D O I
10.1155/2012/410879
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To evaluate the feasibility and advantages of constructing a novel tissue engineering bone, using beta-tricalcium phosphate (beta-TCP) and rat adipose-derived stem cells (ADSCs), modified with BMP2 and BMP7 by lentivirus. In the present study, ADSCs transfected with Lv-BMP2 and Lv-BMP7, alone or together, were seeded on beta-TCP scaffold and cultured in vitro. Based on the results of DNA assay, alkaline phosphatase (ALP) activity, alizarin red staining and osteogenic marker genes expression analysis, the BMP2 and BMP7 genes cotransfection group exhibited a higher degree of osteogenic differentiation in vitro. To investigate the in vivo osteogenesis of the tissue engineering bone, the ADSCs/beta-TCP constructs were implanted in rat femurs defects for 6 weeks and studied histomorphology and radiography. The results showed that BMP2 and BMP7 genes cotransfection group dramatically enhanced the efficiency of new bone formation than BMP2 group and BMP7 group in vivo. These results demonstrated that it was advantageous to construct tissue engineering bone using ADSCs cotransfected with BMP2 and BMP7 on beta-TCP, providing a potential way for treating bone defects.
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页数:7
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