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Functionalization of Ultrabithorax Materials with Vascular Endothelial Growth Factor Enhances Angiogenic Activity.
Howell, David W; Duran, Camille L; Tsai, Shang-Pu; Bondos, Sarah E; Bayless, Kayla J.
  • Howell DW; Department of Molecular and Cellular Medicine, Texas A&M University Health Science Center , College Station, Texas 77843, United States.
  • Duran CL; Department of Molecular and Cellular Medicine, Texas A&M University Health Science Center , College Station, Texas 77843, United States.
  • Tsai SP; Department of Molecular and Cellular Medicine, Texas A&M University Health Science Center , College Station, Texas 77843, United States.
  • Bondos SE; Department of Molecular and Cellular Medicine, Texas A&M University Health Science Center , College Station, Texas 77843, United States.
  • Bayless KJ; Department of Biochemistry and Cell Biology, Rice University , Houston, Texas 77005, United States.
Biomacromolecules ; 17(11): 3558-3569, 2016 11 14.
Article en En | MEDLINE | ID: mdl-27715013
Successful design of tissue engineering scaffolds must include the ability to stimulate vascular development by incorporating angiogenic growth factors. Current approaches can allow diffusion of growth factors, incorporate active factors randomly, or can leave residual toxins. We addressed these problems by genetically fusing the gene encoding Vascular Endothelial Growth Factor (VEGF) with the Ultrabithorax (Ubx) gene to produce fusion proteins capable of self-assembly into materials. We demonstrate that VEGF-Ubx materials enhance human endothelial cell migration, prolong cell survival, and dose-dependently activate the VEGF signaling pathway. VEGF-Ubx fibers attract outgrowing sprouts in an aortic ring assay and induce vessel formation in a chicken embryo chorioallantoic membrane (CAM) assay. Collectively, these results demonstrate that the activity of VEGF remains intact in Ubx materials. This approach could provide an inexpensive and facile mechanism to stimulate and pattern angiogenesis.
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Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Homeodominio / Proteínas de Drosophila / Ingeniería de Tejidos / Factor A de Crecimiento Endotelial Vascular / Morfogénesis Límite: Animals / Humans Idioma: En Año: 2016 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Homeodominio / Proteínas de Drosophila / Ingeniería de Tejidos / Factor A de Crecimiento Endotelial Vascular / Morfogénesis Límite: Animals / Humans Idioma: En Año: 2016 Tipo del documento: Article