2011
DOI: 10.5301/ijao.5000069
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Tissue Engineering of Bladder Using Vascular Endothelial Growth Factor Gene-Modified Endothelial Progenitor Cells

Abstract: VEGF-modified EPCs significantly enhanced neovascularization, compared with BAMG alone. These results indicate that EPCs, combined with VEGF gene therapy, may be a suitable approach for increasing blood supply in the tissue engineering of bladders. Thus, a useful strategy to achieve a tissue-engineered bladder is indicated.

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Cited by 32 publications
(14 citation statements)
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“…Sharma et al also demonstrated that co-transplantation of CD34+ hematopoietic stem/progenitor cells and MSCs resulted in improved and de novo vascularization and peripheral nerve growth in the grafts [37]. Bladder acellular matrix grafts seeded with endothelial progenitor cells modified to express VEGF exhibited enhanced neovascularization in a porcine model of partial cystectomy, suggesting that cell seeding of grafts combined with VEGF gene therapy may be the future of bladder engineering [45]. …”
Section: Bladder Engineeringmentioning
confidence: 99%
“…Sharma et al also demonstrated that co-transplantation of CD34+ hematopoietic stem/progenitor cells and MSCs resulted in improved and de novo vascularization and peripheral nerve growth in the grafts [37]. Bladder acellular matrix grafts seeded with endothelial progenitor cells modified to express VEGF exhibited enhanced neovascularization in a porcine model of partial cystectomy, suggesting that cell seeding of grafts combined with VEGF gene therapy may be the future of bladder engineering [45]. …”
Section: Bladder Engineeringmentioning
confidence: 99%
“…As noted above, a number of studies have explored strategies to ensure appropriate neovascularization, either by optimization of processing strategies to retain bioactive factors in acellular scaffolds or by addition of recombinant angiogenic factors such as FGF-2 or VEGF [95, 106, 108]. In addition to covalent linkage of VEGF recombinant proteins, some investigators have incorporated VEGF plasmid into cells by viral transduction prior to seeding on scaffolds [109, 110] to ensure sustained production of protein following engraftment. These types of experiments exemplify dynamic reciprocity in that the scaffold ECM signals to endothelial cells in the host tissue, which in turn responds by undergoing angiogenesis to vascularize the graft and promote integration into the host organ.…”
Section: Modulation Of Scaffold Properties With Trophic Factorsmentioning
confidence: 99%
“…Cells have been genetically modified for growth factor secretion (e.g., BMP, VEGF, and NGF) ex vivo , seeded on or within naturally-derived scaffolds, and subsequently implanted. 21,37,49,108 There is recent interest in the use of genetically modified mesenchymal stem cells (MSCs) to aid in the transplantation of xenogeneic materials. 73 When delivered in the absence of a scaffold, galactosyl epitope knock-out (Gal-KO) pig MSCs attenuated immune response and improved bone regeneration.…”
Section: Biological Propertiesmentioning
confidence: 99%