In vitro and in vivo induction of bone formation using a recombinant adenoviral vector carrying the human BMP-2 gene

被引:127
作者
Cheng, SL
Lou, J
Wright, NM
Lai, CF
Avioli, LV
Riew, KD [1 ]
机构
[1] Washington Univ, Sch Med, Dept Orthopaed Surg, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Internal Med, Div Bone & Mineral Dis, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Neurol Surg, St Louis, MO USA
关键词
spine fusion; BMP-2; mesenchymal stem cells; adenovirus; gene therapy;
D O I
10.1007/BF02678146
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has been well established that bone morphogenetic protein-2 (BMP-2) can induce bone formation both in vivo and in vitro. although high concentrations (up to milligrams) of BMP-2 have been required to achieve this effect in vivo. Further, clinical applications are usually limited to a single dose at the time of implantation. In an attempt to prolong the transforming effect of BMP-2 we used a recombinant adenoviral vector carrying the human BMP-2 gene (AdV-BMP2) to transduce marrow-derived mesenchymal stem cells (MSC) of skeletally mature male New Zealand white rabbits. The pluripotential MSC were incubated with AdV-BMP2 overnight followed by culture in growth medium for 1 week. Assays on tissue cultures demonstrated that these AdV-BMP2 transduced MSC produced BMP-2 protein, differentiated into an osteoprogenitor line, and induced bone formation in vitro. These MSC had increased alkaline phosphatase activity, increased expression of type I collagen, osteopontin, and osteocalcin mRNA, and induced matrix mineralization compared with both non-transduced cells and cells transduced with a control adenoviral construct. To analyze the osteogenic potential in vivo, Adv-BMP2-transduced MSC were autologously implanted into the intertransverse process space between L5 and L6 of the donor rabbits. The production of new bone was demonstrated by radiographic examination 4 weeks later in areas implanted with cells transduced with AdV-BMP2, whereas no bone was evident at sites implanted with cells transduced with the control adenoviral construct. Histological examination further confirmed the presence of new bone formation. These accumulated data indicate that it is possible to successfully transduce mesenchymal stem cells with a recombinant adenoviral vector carrying the gene for BMP-2 such that these cells will produce BMP-2, differentiate into an osteoprogenitor line, and induce bone formation both in vitro and in vivo. Moreover, incubation of the AdV-BMP2-transduced cells for an additional 7 days in culture before transplantation enhances the success rate in bone formation (three out of three) as compared with our previous report (one out of five, Calcif Tissue Int 63:357-360, 1998).
引用
收藏
页码:87 / 94
页数:8
相关论文
共 21 条
[1]   Video-assisted lateral intertransverse process arthrodesis - Validation of a new minimally invasive lumbar spinal fusion technique in the rabbit and nonhuman primate (rhesus) models [J].
Boden, SD ;
Moskovitz, PA ;
Morone, MA ;
Toribitake, Y .
SPINE, 1996, 21 (22) :2689-2697
[2]   OSTEOPONTIN AND RELATED PHOSPHORYLATED SIALOPROTEINS - EFFECTS ON MINERALIZATION [J].
BOSKEY, AL .
OSTEOPONTIN: ROLE IN CELL SIGNALLING AND ADHESION, 1995, 760 :249-256
[3]  
BOURDEAU JE, 1988, MINER ELECTROL METAB, V14, P253
[4]  
Deodhar AA, 1996, BRIT J RHEUMATOL, V35, P309
[5]   ACIDIC PHOSPHOPROTEINS FROM BONE-MATRIX - A STRUCTURAL RATIONALIZATION OF THEIR ROLE IN BIOMINERALIZATION [J].
GORSKI, JP .
CALCIFIED TISSUE INTERNATIONAL, 1992, 50 (05) :391-396
[6]   T-cells in the pathogenesis of rheumatoid arthritis - Villains or accomplices? [J].
Kinne, RW ;
PalomboKinne, E ;
Emmrich, F .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1997, 1360 (02) :109-141
[7]  
Lecanda F, 1997, J CELL BIOCHEM, V67, P386, DOI 10.1002/(SICI)1097-4644(19971201)67:3<386::AID-JCB10>3.0.CO
[8]  
2-B
[9]   Gene therapy:: Adenovirus-mediated human bone morphogenetic protein-2 gene transfer induces mesenchymal progenitor cell proliferation and differentiation in vitro and bone formation in vivo [J].
Lou, JR ;
Xu, F ;
Merkel, K ;
Manske, P .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1999, 17 (01) :43-50
[10]  
Morone MA, 1998, CLIN ORTHOP RELAT R, P252