Review: Gene- and stem cell-based therapeutics for bone regeneration and repair

被引:119
作者
Kimelman, Nadav
Pelled, Gadi
Helm, Gregory A.
Huard, J.
Schwarz, Edward M.
Gazit, Dan
机构
[1] Hebrew Univ Jerusalem, Skeletal Biotech Lab, Jerusalem, Israel
[2] Univ Virginia, Hlth Sci Ctr, Dept Neurol Surg, Charlottesville, VA 22908 USA
[3] Univ Pittsburgh, Childrens Hosp Pittsburgh, Dept Orthopaed Surg, Growth & Dev Lab, Pittsburgh, PA 15213 USA
[4] Univ Rochester, Med Ctr, Ctr Musculoskeletal Res, Rochester, NY 14627 USA
[5] Cedars Sinai Med Ctr, Dept Surg, Los Angeles, CA USA
[6] Cedars Sinai Med Ctr, Int Stem Cell Inst, Los Angeles, CA USA
来源
TISSUE ENGINEERING | 2007年 / 13卷 / 06期
关键词
D O I
10.1089/ten.2007.0096
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Many clinical conditions require regeneration or implantation of bone. This is one focus shared by neurosurgery and orthopedics. Current therapeutic options (bone grafting and protein-based therapy) do not provide satisfying solutions to the problem of massive bone defects. In the past few years, gene- and stem cell-based therapy has been extensively studied to achieve a viable alternative to current solutions offered by modern medicine for bone-loss repair. The use of adult stem cells for bone regeneration has gained much focus. This unique population of multipotential cells has been isolated from various sources, including bone marrow, adipose, and muscle tissues. Genetic engineering of adult stem cells with potent osteogenic genes has led to fracture repair and rapid bone formation in vivo. It is hypothesized that these genetically modified cells exert both an autocrine and a paracrine effects on host stem cells, leading to an enhanced osteogenic effect. The use of direct gene delivery has also shown much promise for in vivo bone repair. Several viral and nonviral methods have been used to achieve substantial bone tissue formation in various sites in animal models. To advance these platforms to the clinical setting, it will be mandatory to overcome specific hurdles, such as control over transgene expression, viral vector toxicity, and prolonged culture periods of therapeutic stem cells. This review covers a prospect of cell and gene therapy for bone repair as well as some very recent advancements in stem cell isolation, genetic engineering, and exogenous control of transgene expression.
引用
收藏
页码:1135 / 1150
页数:16
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