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Nanobiomechanics of Repair Bone Regenerated by Genetically Modified Mesenchymal Stem Cells
Journal article   Open access   Peer reviewed

Nanobiomechanics of Repair Bone Regenerated by Genetically Modified Mesenchymal Stem Cells

Kuangshin Tai, Gadi Pelled, Dima Sheyn, Anna Bershteyn, Lin Han, Ilan Kallai, Yoram Zilberman, Christine Ortiz and Dan Gazit
Tissue engineering. Part A, v 14(10), pp 1709-1720
01 Oct 2008
PMID: 18620480
url
http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.363.6507View

Abstract

Cell & Tissue Engineering Cell Biology Engineering Engineering, Biomedical Life Sciences & Biomedicine Materials Science Materials Science, Biomaterials Science & Technology Technology
Genetically modified mesenchymal stem cells (MSCs), overexpressing a BMP gene, have been previously shown to be potent inducers of bone regeneration. However, little was known of the chemical and intrinsic nanomechanical properties of this engineered bone. A previous study utilizing microcomputed tomography, back-scattered electron microscopy, energy-dispersive X-ray, nanoindentation, and atomic force microscopy showed that engineered ectopic bone, although similar in chemical composition and topography, demonstrated an elastic modulus range (14.6-22.1 GPa) that was less than that of the native bone (16.6-38.5 GPa). We hypothesized that these results were obtained due to the specific conditions that exist in an intramuscular ectopic implantation site. Here, we implanted MSCs overexpressing BMP-2 gene in an orthotopic site, a nonunion radial bone defect, in mice. The regenerated bone tissue was analyzed using the same methods previously utilized. The samples revealed high similarity between the engineered and native radii in chemical structure and elemental composition. In contrast to the previous study, nanoindentation data showed that, in general, the native bone exhibited a statistically similar elastic modulus values compared to that of the engineered bone, while the hardness was found to be marginally statistically different at 1000 mu N and statistically similar at 7000 mu N. We hypothesize that external loading, osteogenic cytokines and osteoprogenitors that exist in a fracture site could enhance the maturation of engineered bone derived from BMP-modified MSCs. Further studies should determine whether longer duration periods postimplantation would lead to increased bone adaptation.

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Collaboration types
Domestic collaboration
International collaboration
Web of Science research areas
Cell & Tissue Engineering
Cell Biology
Engineering, Biomedical
Materials Science, Biomaterials
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