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Enhancement of bone formation by genetically-engineered bone marrow stromal cells expressing BMP-2, VEGF and angiopoietin-1

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Abstract

To explore the potential of combined delivery of osteogenic and angiogenic factors to bone marrow stromal cells (BMSCs) for repair of critical-size bone defects, we followed the formation of bone and vessels in tissue-engineered constructs in nude mice and rabbit bone defects upon introducing different combinations of BMP-2, vascular endothelial growth factor (VEGF) and angiopoietin-1 (Ang-1) to BMSCs with adenoviral vectors. Better osteogenesis and angiogenesis were found in co-delivery group of BMP-2, VEGF and angiopoietin-1 than any other combination of these factors in both animal models, indicating combined gene delivery of angiopoietin-1 and VEGF165 into a tissue-engineered construct produces an additive effect on BMP-2-induced osteogenesis.

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References

  • Chae JK, Kim J, Lim ST et al (2000) Coadministration of angiopoietin-1 and vascular endothelial growth factor enhances collateral vascularization. Arterioscler Thromb Vasc Biol 20:2573–2578

    PubMed  CAS  Google Scholar 

  • Gerber HP, Vu TH, Ryan AM et al (1999) VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation. Nat Med 5:623–628

    Article  PubMed  CAS  Google Scholar 

  • Lee RJ, Springer ML, Blanco-Bose WE et al (2000) VEGF gene delivery to myocardium: deleterious effects of unregulated expression. Circulation 102(8):898–901

    PubMed  CAS  Google Scholar 

  • Levy RJ, Goldstein SA, Bonadio J (1998) Gene therapy for tissue repair and regeneration. Adv Drug Deliv Rev 33(1–2):53–69

    PubMed  Google Scholar 

  • Masaki I, Yonemitsu Y, Yamashita A et al (2002) Angiogenic gene therapy for experimental critical limb ischemia: acceleration of limb loss by overexpression of vascular endothelial growth factor 165 but not of fibroblast growth factor 2. Circ Res 90:966–973

    Article  PubMed  CAS  Google Scholar 

  • Murphy WL, Mooney DJ (1999) Controlled delivery of inductive proteins, plasmid DNA and cells from tissue engineering matrices. J Periodontal Res 34:413–419

    Article  PubMed  CAS  Google Scholar 

  • Peng H, Wright V, Usas A et al (2002) Synergistic enhancement of bone formation and healing by stem cell-expressed VEGF and bone morphogenetic protein-4. J Clin Invest 110(6):751–759

    PubMed  CAS  Google Scholar 

  • Schwartz ER, Speakman MT, Patterson M et al (2000) Evaluation of the effects of intramyocardial injection of DNA expressing vascular endothelial growth factor (VEGF) in a myocardial infarction model in the rat—angiogenesis and angioma formation. J Am Coll Cardiol 35:1323–1330

    Article  Google Scholar 

  • Thurston G, Suri C, Smith K et al (1999) Leakage-resistant blood vessels in mice transgenically overexpressing angiopoietin-1. Science 286:2511–2514

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Kerong Dai.

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Hou, H., Zhang, X., Tang, T. et al. Enhancement of bone formation by genetically-engineered bone marrow stromal cells expressing BMP-2, VEGF and angiopoietin-1. Biotechnol Lett 31, 1183–1189 (2009). https://doi.org/10.1007/s10529-009-0007-4

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  • DOI: https://doi.org/10.1007/s10529-009-0007-4

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