Ex Vivo Gene Therapy to Produce Bone Using Different Cell Types

Gene therapy and tissue engineering promise to revolutionize orthopaedic surgery. This study comprehensively compares five different cell types in ex vivo gene therapy to produce bone. The cell types include a bone marrow stromal cell line, primary muscle derived cells, primary bone marrow stromal cells, primary articular chondrocytes, and primary fibroblasts. After transduction by an adenovirus encoding for bone morphogenetic protein-2, all of the cell types were capable of secreting bone morphogenetic protein-2. However, the bone marrow stromal cell line and muscle derived cells showed more responsiveness to recombinant human bone morphogenetic protein-2 than did the other cell types. In vivo injection of each of the cell populations transduced to secrete bone morphogenetic protein-2 resulted in bone formation. Radiographic and histologic analyses corroborated the in vitro data regarding bone morphogenetic protein-2 secretion and cellular osteocompetence. This study showed the feasibility of using primary bone marrow stromal cells, primary muscle derived cells, primary articular chondrocytes, primary fibroblasts, and an osteogenesis imperfecta stromal cell line in ex vivo gene therapy to produce bone. The study also showed the advantages and disadvantages inherent in using each cell type.

[1]  P. Robbins,et al.  Adenovirus-mediated direct gene therapy with bone morphogenetic protein-2 produces bone. , 1999, Bone.

[2]  J. Lou,et al.  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 , 1999, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[3]  J. Wozney,et al.  Effects of recombinant human bone morphogenetic protein-2 on differentiation of cells isolated from human bone, muscle, and skin. , 1998, Bone.

[4]  D. Grande,et al.  Expression of human bone morphogenic protein 7 in primary rabbit periosteal cells: potential utility in gene therapy for osteochondral repair , 1998, Gene Therapy.

[5]  G. Finerman,et al.  Regional gene therapy with a BMP‐2‐producing murine stromal cell line induces heterotopic and orthotopic bone formation in rodents , 1998, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[6]  J. Wozney,et al.  Bone Formation with Use of rhBMP-2 (Recombinant Human Bone Morphogenetic Protein-2)* , 1997, The Journal of bone and joint surgery. American volume.

[7]  E. Morris,et al.  The Effect of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP-2) on the Healing of Full-Thickness Defects of Articular Cartilage* , 1997, The Journal of bone and joint surgery. American volume.

[8]  J. Greenberger,et al.  Effect of rhBMP-2 on the osteogenic potential of bone marrow stromal cells from an osteogenesis imperfecta mouse (oim). , 1997, Bone.

[9]  J. Wozney,et al.  Recombinant bone morphogenetic protein (BMP)‐2 regulates costochondral growth plate chondrocytes and induces expression of BMP‐2 and BMP‐4 in a cell maturation‐dependent manner , 1997, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[10]  M. Kitamura,et al.  Construction of adenovirus vectors through Cre-lox recombination , 1997, Journal of virology.

[11]  R. Hewick,et al.  Recombinant human bone morphogenetic protein‐2 maintains the articular chondrocyte phenotype in long‐term culture , 1996, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[12]  L. Gilula,et al.  Repair of calvarial defects with flap tissue: role of bone morphogenetic proteins and competent responding tissues. , 1996, Plastic and reconstructive surgery.

[13]  S. Goldstein,et al.  Stimulation of new bone formation by direct transfer of osteogenic plasmid genes. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[14]  H. E. Young,et al.  A population of cells isolated from rat heart capable of differentiating into several mesodermal phenotypes. , 1996, The Journal of surgical research.

[15]  T. Aigner,et al.  Osteogenic differentiation of hypertrophic chondrocytes involves asymmetric cell divisions and apoptosis , 1995, The Journal of cell biology.

[16]  P. Robbins,et al.  Possible orthopaedic applications of gene therapy. , 1995, The Journal of bone and joint surgery. American volume.

[17]  J. Smith,et al.  Mesenchymal stem cells reside within the connective tissues of many organs , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[18]  V. Rosen,et al.  Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage [published erratum appears in J Cell Biol 1995 Feb;128(4):following 713] , 1994, The Journal of cell biology.

[19]  A. Reddi Bone and cartilage differentiation. , 1994, Current opinion in genetics & development.

[20]  H. Blau,et al.  Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy , 1994, The Journal of cell biology.

[21]  A. Reddi,et al.  Reconstruction of the Bone‐Bone Marrow Organ by Osteogenin, a Bone Morphogenetic Protein, and Demineralized Bone Matrix in Calvarial Defects of Adult Primates , 1993, Plastic and reconstructive surgery.

[22]  Arnold I. Caplan,et al.  Mesenchymal Stem Cells , 1991, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[23]  U. Ripamonti The induction of bone in osteogenic composites of bone matrix and porous hydroxyapatite replicas: an experimental study on the baboon (Papio ursinus). , 1991, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons.

[24]  J. Heckman,et al.  The use of bone morphogenetic protein in the treatment of non-union in a canine model. , 1991, The Journal of bone and joint surgery. American volume.

[25]  V. Rosen,et al.  Recombinant human bone morphogenetic protein-2 stimulates osteoblastic maturation and inhibits myogenic differentiation in vitro , 1991, The Journal of cell biology.

[26]  F W Neukam,et al.  Bone replacement with porous hydroxyapatite blocks and titanium screw implants: an experimental study. , 1991, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons.

[27]  V. Rosen,et al.  Recombinant human bone morphogenetic protein induces bone formation. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[28]  V. Rosen,et al.  Novel regulators of bone formation: molecular clones and activities. , 1988, Science.

[29]  G. Finerman,et al.  Repair of segmental defects of the tibia with cancellous bone grafts augmented with human bone morphogenetic protein. A preliminary report. , 1988, Clinical orthopaedics and related research.

[30]  M. Urist,et al.  Bone morphogenetic protein augmentation grafting of resistant femoral nonunions. A preliminary report. , 1988, Clinical orthopaedics and related research.

[31]  J. Sanes,et al.  Use of a recombinant retrovirus to study post‐implantation cell lineage in mouse embryos. , 1986, The EMBO journal.

[32]  D. Gazit,et al.  Kinetics and differentiation of marrow stromal cells in diffusion chambers in vivo. , 1986, Journal of cell science.

[33]  M. Urist,et al.  Experimental myositis ossificans: cartilage and bone formation in muscle in response to a diffusible bone matrix-derived morphogen. , 1978, Archives of pathology & laboratory medicine.

[34]  W. T. Green,et al.  Behavior of articular chondrocytes in cell culture. , 1971, Clinical orthopaedics and related research.

[35]  M. Urist,et al.  Bone: Formation by Autoinduction , 1965, Science.

[36]  R. R. Bensley,et al.  Embryonic Development and Induction , 1938, The Yale Journal of Biology and Medicine.

[37]  N. Takahashi,et al.  Bone Morphogenetic Protein-2 Converts the Differentiation Pathway of C2C12 Myoblasts into the Osteoblast Lineage , 2002 .

[38]  D. Kallmes,et al.  Percutaneous spinal fusion using bone morphogenetic protein-2 gene therapy. , 1999, Journal of neurosurgery.

[39]  A. Huvos,et al.  Expression of bone morphogenetic proteins in human osteosarcoma. Immunohistochemical detection with monoclonal antibody , 1994, Cancer.

[40]  A I Caplan,et al.  Characterization of cells with osteogenic potential from human marrow. , 1992, Bone.

[41]  P. Nijweide,et al.  Tartrate-resistant acid phosphatase is not an exclusive marker for mouse osteoclasts in cell culture. , 1991, Bone.