Enhancement of bone formation by genetically-engineered bone marrow stromal cells expressing BMP-2, VEGF and angiopoietin-1

被引:26
|
作者
Hou, Hongliang [1 ]
Zhang, Xiaoling [2 ]
Tang, Tingting [1 ]
Dai, Kerong [1 ,2 ]
Ge, Ruowen [3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Dept Orthopaed, Shanghai 200011, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Hlth Sci, Shanghai 200025, Peoples R China
[3] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
关键词
Angiopoietin-1; Bone morphogenic protein 2; Bone tissue engineering; Critical-size bone defect; Vascular endothelial growth factor; ANGIOGENESIS; DELIVERY; DNA;
D O I
10.1007/s10529-009-0007-4
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 explore the potential of combined delivery of osteogenic and angiogenic factors to bone marrow stromal cells (BMSCs) for repair of critical-size bone defects, we followed the formation of bone and vessels in tissue-engineered constructs in nude mice and rabbit bone defects upon introducing different combinations of BMP-2, vascular endothelial growth factor (VEGF) and angiopoietin-1 (Ang-1) to BMSCs with adenoviral vectors. Better osteogenesis and angiogenesis were found in co-delivery group of BMP-2, VEGF and angiopoietin-1 than any other combination of these factors in both animal models, indicating combined gene delivery of angiopoietin-1 and VEGF165 into a tissue-engineered construct produces an additive effect on BMP-2-induced osteogenesis.
引用
收藏
页码:1183 / 1189
页数:7
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