Immunoselection and adenoviral genetic modulation of human osteoprogenitors: in vivo bone formation on PLA scaffold

被引:77
作者
Howard, D
Partridge, K
Yang, XB
Clarke, NMP
Okubo, Y
Bessho, K
Howdle, SM
Shakesheff, KM
Oreffo, ROC [1 ]
机构
[1] Univ Southampton, Univ Orthopaed, Southampton SO16 6YD, Hants, England
[2] Kyoto Univ, Grad Sch Med, Dept Oral & Maxillofacial Surg, Sakyo Ku, Kyoto 6068507, Japan
[3] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[4] Univ Nottingham, Sch Pharmaceut Sci, Nottingham NG7 2RD, England
基金
英国生物技术与生命科学研究理事会;
关键词
osteoprogenitor; mesenchymal stem cell; immunoselection; STRO-1 monoclonal antibody; adenoviral gene-transfer; bone morphogenetic protein-2; biodegradable polymer; poly(D; L-lactic acid); tissue engineering;
D O I
10.1016/S0006-291X(02)02561-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to examine the potential of immunoselected genetically modified human osteoprogenitors to form bone in vivo on porous PLA scaffolds. Human osteoprogenitors from bone marrow were selected using the antibody STRO-1 Utilising a magnetically activated cell separation system. The STRO-1(-) fraction isolated 7% of nucleated marrow cells and increased fibroblastic colony formation by 300% and alkaline phosphatase activity by 190% over unselected marrow cell Cultures. To engineer bone tissue, STRO-1(+) culture-expanded cells were transduced with AxCAOBMP-2. an adenovirus carrying the human BMP-2 gene, injected into diffusion chambers containing porous PLA scaffolds. and implanted in vivo, After 11 weeks the presence of bone mineral was observed by X-ray analysis and confirmed for mineral by von Kossa. as well as bone matrix composition by Sirius red staining, birefringence, and type I collagen immunohistochemistry. Bone formation in vivo indicates the potential of using immunoselected progenitor cells and ex vivo gene transfer with biodegradable scaffolds, for the development of protocols for the treatment of a wide variety of musculo-skeletal disorders. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:208 / 215
页数:8
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