Mesenchymal stem cell-mediated gene delivery of bone morphogenetic protein-2 in an articular fracture model

被引:63
|
作者
Zachos, Terri
Diggs, Alisha
Weisbrode, Steven
Bartlett, Jeffrey
Bertone, Alicia
机构
[1] Ohio State Univ, Dept Vet Clin Sci, Comparat Orthoped Mol & Appl Res Labs, Columbus, OH 43210 USA
[2] Univ Michigan, Dept Biomed Engn, Scaffold Engn Lab, Ann Arbor, MI 48109 USA
[3] Ohio State Univ, Dept Vet Biosci, Columbus, OH 43210 USA
[4] Columbus Childrens Res Inst, Ctr Gene Therapy, Columbus, OH USA
关键词
D O I
10.1038/sj.mt.6300192
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
In articular fractures, both bone and cartilage are injured. We tested whether stem cells transduced with bone morphogenetic protein 2 (BMP2) can promote bone and cartilage repair. Distal femoral articular osteotomies in nude rats were treated with stem cells, either wild-type or transduced with an adenoviral (Ad) BMP2. Cells were delivered in alginate (ALG) carrier or by direct injection in saline solution. Gene expression of these cells at the osteotomy site was confirmed by in vivo imaging. At day 14, only the group that received AdBMP2 stem cells by direct injection showed completely healed osteotomies, while other groups remained unhealed (P < 0.0003). In ALG groups, bone healing was impeded by the development of a chondroid mass, most pronounced in the AdBMP2 ALG group (P < 0.002). We were successful in achieving repair of both bone and cartilage in vivo using direct stem cell injection. Our data suggests that BMP2 augmentation might be critically important in achieving this effect.
引用
收藏
页码:1543 / 1550
页数:8
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