TY - JOUR
T1 - Engineered human mesenchymal stem cells
T2 - A novel platform for skeletal cell mediated gene therapy
AU - Turgeman, Gadi
AU - Pittman, Debbie D.
AU - Müller, Ralph
AU - Kurkalli, Basan Gowda
AU - Zhou, Shuanhu
AU - Pelled, Gadi
AU - Peyser, Amos
AU - Zilberman, Yoram
AU - Moutsatsos, Ioannis K.
AU - Gazit, Dan
PY - 2001/5
Y1 - 2001/5
N2 - Background Human mesenchymal stem cells (hMSCs) are pluripotent cells that can differentiate to various mesenchymal cell types. Recently, a method to isolate hMSCs from bone marrow and expand them in culture was described. Here we report on the use of hMSCs as a platform for gene therapy aimed at bone lesions. Methods Bone marrow derived hMSCs were expanded in culture and infected with recombinant adenoviral vector encoding the osteogenic factor, human BMP-2. The osteogenic potential of genetically engineered hMSCs was assessed in vitro and in vivo. Results Genetically engineered hMSCs displayed enhanced proliferation and osteogenic differentiation in culture. In vivo, transplanted genetically engineered hMSCs were able to engraft and form bone and cartilage in ectopic sites, and regenerate bone defects (non-union fractures) in mice radius bone. Importantly, the same results were obtained with hMSCs isolated from a patient suffering from osteoporosis. Conclusions hMSCs represent a novel platform for skeletal gene therapy and the present results suggest that they can be genetically engineered to express desired therapeutic proteins inducing specific differentiation pathways. Moreover, hMSCs obtained from osteoporotic patients can restore their osteogenic activity following human BMP-2 gene transduction, an important finding in the future planning of gene therapy treatment for osteoporosis.
AB - Background Human mesenchymal stem cells (hMSCs) are pluripotent cells that can differentiate to various mesenchymal cell types. Recently, a method to isolate hMSCs from bone marrow and expand them in culture was described. Here we report on the use of hMSCs as a platform for gene therapy aimed at bone lesions. Methods Bone marrow derived hMSCs were expanded in culture and infected with recombinant adenoviral vector encoding the osteogenic factor, human BMP-2. The osteogenic potential of genetically engineered hMSCs was assessed in vitro and in vivo. Results Genetically engineered hMSCs displayed enhanced proliferation and osteogenic differentiation in culture. In vivo, transplanted genetically engineered hMSCs were able to engraft and form bone and cartilage in ectopic sites, and regenerate bone defects (non-union fractures) in mice radius bone. Importantly, the same results were obtained with hMSCs isolated from a patient suffering from osteoporosis. Conclusions hMSCs represent a novel platform for skeletal gene therapy and the present results suggest that they can be genetically engineered to express desired therapeutic proteins inducing specific differentiation pathways. Moreover, hMSCs obtained from osteoporotic patients can restore their osteogenic activity following human BMP-2 gene transduction, an important finding in the future planning of gene therapy treatment for osteoporosis.
KW - Adenovirus
KW - Bone formation
KW - Bone regeneration
KW - Gene therapy
KW - Human mesenchymal stem cell
KW - RhBMP-2
UR - http://www.scopus.com/inward/record.url?scp=0035345628&partnerID=8YFLogxK
U2 - 10.1002/1521-2254(200105/06)3:3<240::AID-JGM181>3.0.CO;2-A
DO - 10.1002/1521-2254(200105/06)3:3<240::AID-JGM181>3.0.CO;2-A
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C2 - 11437329
AN - SCOPUS:0035345628
SN - 1099-498X
VL - 3
SP - 240
EP - 251
JO - Journal of Gene Medicine
JF - Journal of Gene Medicine
IS - 3
ER -