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

被引:162
作者
Lou, JR [1 ]
Xu, F [1 ]
Merkel, K [1 ]
Manske, P [1 ]
机构
[1] Washington Univ, Sch Med, Dept Orthopaed Surg, St Louis, MO 63110 USA
关键词
D O I
10.1002/jor.1100170108
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
This study reports that recombinant adenovirus-mediated human bone morphogenetic protein-2 gene transfer can induce mesenchymal progenitor cell differentiation and bone formation. The recombinant adenovirus with the human bone morphogenetic protein-2 gene was constructed, and mature human bone morphogenetic protein-2 expression mediated by adenovirus gene transfer was detected by specific antibody. Under adenovirus-mediated bone morphogenetic-protein gene transfer, mesenchymal progenitor cell line C3H/10T 1/2 showed cell proliferation dependent on adenovirus bone morphogenetic-protein dose. The C3H/10T 1/2 cells transduced by adenovirus bone morphogenetic protein also exhibited differentiation to osteoblast phenotype, which indicates alkaline phosphatase activity. Injection of the C3H/10T 1/2 cells into the thigh muscles of nude mice led to ossicle development detectable on radiographs, Histological analysis indicated that the new ossicles that developed in the thigh muscles of the mice had different osseous components including bone trabeculae, bone marrow, and chondrified tissue. The results of this study demonstrate the potential for gene therapy by adenovirus-mediated bone morphogenetic-protein gene transfer.
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页码:43 / 50
页数:8
相关论文
共 27 条
[1]   EXPRESSION OF HUMAN BONE MORPHOGENETIC PROTEINS-2 OR PROTEINS-4 IN MURINE MESENCHYMAL PROGENITOR C3H10T1/2 CELLS INDUCES DIFFERENTIATION INTO DISTINCT MESENCHYMAL CELL LINEAGES [J].
AHRENS, M ;
ANKENBAUER, T ;
SCHRODER, D ;
HOLLNAGEL, A ;
MAYER, H ;
GROSS, G .
DNA AND CELL BIOLOGY, 1993, 12 (10) :871-880
[2]  
BERESFORD JN, 1989, CLIN ORTHOP RELAT R, P270
[3]   CELLULAR AND MOLECULAR EVENTS DURING EMBRYONIC BONE-DEVELOPMENT [J].
BRUDER, SP ;
CAPLAN, AI .
CONNECTIVE TISSUE RESEARCH, 1989, 20 (1-4) :65-71
[4]   1ST BONE-FORMATION AND THE DISSECTION OF AN OSTEOGENIC LINEAGE IN THE EMBRYONIC CHICK TIBIA IS REVEALED BY MONOCLONAL-ANTIBODIES AGAINST OSTEOBLASTS [J].
BRUDER, SP ;
CAPLAN, AI .
BONE, 1989, 10 (05) :359-375
[5]  
CAPLAN AI, 1992, BIOL MECH TOOTH MOVE, P433
[6]   IN-VIVO EVALUATION OF RECOMBINANT HUMAN OSTEOGENIC PROTEIN (RHOP-1) IMPLANTS AS A BONE-GRAFT SUBSTITUTE FOR SPINAL FUSIONS [J].
COOK, SD ;
DALTON, JE ;
TAN, EH ;
WHITECLOUD, TS ;
RUEGER, DC .
SPINE, 1994, 19 (15) :1655-1663
[7]  
GERHART TN, 1993, CLIN ORTHOP RELAT R, P317
[8]   RECOMBINANT VGR-1 BMP-6 EXPRESSING TUMORS INDUCE FIBROSIS AND ENDOCHONDRAL BONE-FORMATION IN-VIVO [J].
GITELMAN, SE ;
KOBRIN, MS ;
YE, JQ ;
LOPEZ, AR ;
LEE, A ;
DERYNCK, R .
JOURNAL OF CELL BIOLOGY, 1994, 126 (06) :1595-1609
[9]  
GOSHIMA J, 1991, CLIN ORTHOP RELAT R, P274
[10]   CHARACTERIZATION OF CELLS WITH OSTEOGENIC POTENTIAL FROM HUMAN MARROW [J].
HAYNESWORTH, SE ;
GOSHIMA, J ;
GOLDBERG, VM ;
CAPLAN, AI .
BONE, 1992, 13 (01) :81-88