“…Several studies have focused on a controlled delivery of growth factors over a longer duration of time in order to simulate the natural sequestration of growth factors in native body. VEGF and Ang-1 were delivered in a hydrogel to elicit vascular maturity in rat aortic rings [43]. Mooney and colleagues have devised several strategies to deliver multiple growth factors through controlled release either by incorporating the growth factors directly or seeding endothelial cells into polymeric scaffolds that in turn release the growth factors in a controlled fashion.…”
Section: Growth Factor Incorporation By Deliverymentioning
A key challenge in tissue engineering is overcoming cell death in the scaffold interior due to the limited diffusion of oxygen and nutrients therein. We hypothesized here that immobilizing a gradient of vascular endothelial growth factor would guide endothelial cells into the interior of the scaffold thereby enhancing angiogenesis. The protein was immobilized onto a collagen scaffold through carbodiimide chemistry by one of the three methods experimented: placing 5 µl of the solution at the center of the scaffold to create a ~2 ng/ml/mm gradient in a radial direction. D4T endothelial cells were observed to be guided by this VEGF-165 gradient deep into the center of the scaffold compared to both uniformly immobilized VEGF-165 and VEGFfree controls. We concluded that the VEGF-165 gradient scaffolds promoted the migration, and not proliferation, of cells deep into the scaffold. These gradient scaffolds provide the foundation for future in vivo tissue engineering studies.iii
“…Several studies have focused on a controlled delivery of growth factors over a longer duration of time in order to simulate the natural sequestration of growth factors in native body. VEGF and Ang-1 were delivered in a hydrogel to elicit vascular maturity in rat aortic rings [43]. Mooney and colleagues have devised several strategies to deliver multiple growth factors through controlled release either by incorporating the growth factors directly or seeding endothelial cells into polymeric scaffolds that in turn release the growth factors in a controlled fashion.…”
Section: Growth Factor Incorporation By Deliverymentioning
A key challenge in tissue engineering is overcoming cell death in the scaffold interior due to the limited diffusion of oxygen and nutrients therein. We hypothesized here that immobilizing a gradient of vascular endothelial growth factor would guide endothelial cells into the interior of the scaffold thereby enhancing angiogenesis. The protein was immobilized onto a collagen scaffold through carbodiimide chemistry by one of the three methods experimented: placing 5 µl of the solution at the center of the scaffold to create a ~2 ng/ml/mm gradient in a radial direction. D4T endothelial cells were observed to be guided by this VEGF-165 gradient deep into the center of the scaffold compared to both uniformly immobilized VEGF-165 and VEGFfree controls. We concluded that the VEGF-165 gradient scaffolds promoted the migration, and not proliferation, of cells deep into the scaffold. These gradient scaffolds provide the foundation for future in vivo tissue engineering studies.iii
“…For example, wound healing was accelerated in a diabetic mouse model when basic fibroblast growth factor was continuously released from the CMHA-S hydrogels into full-thickness wounds. 23,40 Other proteins and small molecules that have been delivered both in vitro and in vivo from these CMHA-S gels and films include the following growth factors: 28,[41][42][43][44][45] Basic…”
Section: Translational Experience To Datementioning
“…These microvessels organized into recognizable tubular networks filled with erythrocytes [33]. Inclusion of heparin by covalently binding it with HA-based hydrogel proved to be more optimized in providing a greater angiogenic response [31,32,34]. Heparin is a highly sulfated GAG known for its affinity for a variety of angiogenic growth factors and ability to sequester those growth factors in the ECM.…”
Section: Hydrogels In Therapeutic Angiogenesismentioning
confidence: 98%
“…While the high molecular weight HA has inhibitory angiogenic effects, the low ones stimulate endothelial cell proliferation and migration [28][29][30]. Chemically modified forms of HA have been developed to form biocompatible, macroporous hydrogel to store and release growth factors in vivo [31][32][33][34]. HA hydrogels carrying both VEGF and keratinocyte growth factor (KGF) upon transplantation into ear pinnae of mice generated intact microvessel beds with well-defined borders.…”
Section: Hydrogels In Therapeutic Angiogenesismentioning
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.