Matches in SemOpenAlex for { <https://semopenalex.org/work/W4210539705> ?p ?o ?g. }
Showing items 1 to 75 of
75
with 100 items per page.
- W4210539705 endingPage "398" @default.
- W4210539705 startingPage "397" @default.
- W4210539705 abstract "INTRODUCTION AND OBJECTIVES This study sought to utilize growth factors to promote the migration of smooth muscle cells (SMC) into an electrospun vascular scaffold. The hypothesis was that the use of growth factors would allow for acellular tissue-engineered vascular grafts that are capable of recruiting smooth muscle cellular proliferation and infiltration in situ. METHODS Scaffolds electrospun with poly(ε-caprolactone) (PCL)/collagen polymers were surface modified through the passive adsorption of platelet-derived growth factor with two beta subunits (PDGF-BB) and stromal derived growth factor 1α (SDF-1α) at various concentrations, individually and together. Single-factor studies investigated each factor at concentrations of 100 ng/mL, 250 ng/mL, and 500 ng/mL. Dual-factor studies investigated the combined effects of 100 ng/mL PDGF-BB and 500 ng/mL of SDF-1α. RESULTS Compared to unmodified controls, scaffolds modified with growth factors showed higher rates of smooth muscle cell proliferation. Notably, scaffolds bioconjugated with a concentration of 100 ng/mL PDGF-BB alone and a concentration of 500 ng/mL SDF-1α alone demonstrated the greatest degree of smooth muscle cell proliferation compared to other single-factor concentrations, which confirmed ideal concentrations reported by other studies. A novel finding was that the combination of these growth factors at the aforementioned concentrations showed synergy in the ability to increase the degree of SMC migration into the depth of the electrospun scaffold. CONCLUSIONS This series of experiments verifies that growth factors promote proliferation of SMCs on an electrospun scaffold, and that combining multiple factors can optimize migration of SMCs farther into the thickness of electrospun scaffolds in an in vitro setting. This study sought to utilize growth factors to promote the migration of smooth muscle cells (SMC) into an electrospun vascular scaffold. The hypothesis was that the use of growth factors would allow for acellular tissue-engineered vascular grafts that are capable of recruiting smooth muscle cellular proliferation and infiltration in situ. Scaffolds electrospun with poly(ε-caprolactone) (PCL)/collagen polymers were surface modified through the passive adsorption of platelet-derived growth factor with two beta subunits (PDGF-BB) and stromal derived growth factor 1α (SDF-1α) at various concentrations, individually and together. Single-factor studies investigated each factor at concentrations of 100 ng/mL, 250 ng/mL, and 500 ng/mL. Dual-factor studies investigated the combined effects of 100 ng/mL PDGF-BB and 500 ng/mL of SDF-1α. Compared to unmodified controls, scaffolds modified with growth factors showed higher rates of smooth muscle cell proliferation. Notably, scaffolds bioconjugated with a concentration of 100 ng/mL PDGF-BB alone and a concentration of 500 ng/mL SDF-1α alone demonstrated the greatest degree of smooth muscle cell proliferation compared to other single-factor concentrations, which confirmed ideal concentrations reported by other studies. A novel finding was that the combination of these growth factors at the aforementioned concentrations showed synergy in the ability to increase the degree of SMC migration into the depth of the electrospun scaffold. This series of experiments verifies that growth factors promote proliferation of SMCs on an electrospun scaffold, and that combining multiple factors can optimize migration of SMCs farther into the thickness of electrospun scaffolds in an in vitro setting." @default.
- W4210539705 created "2022-02-08" @default.
- W4210539705 creator A5030802910 @default.
- W4210539705 creator A5065188585 @default.
- W4210539705 creator A5066336641 @default.
- W4210539705 creator A5066549957 @default.
- W4210539705 creator A5091531148 @default.
- W4210539705 date "2022-02-01" @default.
- W4210539705 modified "2023-10-18" @default.
- W4210539705 title "Role Of Growth Factors In Smooth Muscle Cell Migration In Tissue Engineered Vascular Grafts" @default.
- W4210539705 doi "https://doi.org/10.1016/j.avsg.2021.12.045" @default.
- W4210539705 hasPublicationYear "2022" @default.
- W4210539705 type Work @default.
- W4210539705 citedByCount "0" @default.
- W4210539705 crossrefType "journal-article" @default.
- W4210539705 hasAuthorship W4210539705A5030802910 @default.
- W4210539705 hasAuthorship W4210539705A5065188585 @default.
- W4210539705 hasAuthorship W4210539705A5066336641 @default.
- W4210539705 hasAuthorship W4210539705A5066549957 @default.
- W4210539705 hasAuthorship W4210539705A5091531148 @default.
- W4210539705 hasConcept C12554922 @default.
- W4210539705 hasConcept C126322002 @default.
- W4210539705 hasConcept C136229726 @default.
- W4210539705 hasConcept C16930146 @default.
- W4210539705 hasConcept C170493617 @default.
- W4210539705 hasConcept C180361614 @default.
- W4210539705 hasConcept C185592680 @default.
- W4210539705 hasConcept C2775960820 @default.
- W4210539705 hasConcept C2779395532 @default.
- W4210539705 hasConcept C2781294074 @default.
- W4210539705 hasConcept C2992686903 @default.
- W4210539705 hasConcept C49892992 @default.
- W4210539705 hasConcept C55493867 @default.
- W4210539705 hasConcept C62112901 @default.
- W4210539705 hasConcept C71924100 @default.
- W4210539705 hasConcept C86803240 @default.
- W4210539705 hasConcept C89429830 @default.
- W4210539705 hasConcept C95444343 @default.
- W4210539705 hasConceptScore W4210539705C12554922 @default.
- W4210539705 hasConceptScore W4210539705C126322002 @default.
- W4210539705 hasConceptScore W4210539705C136229726 @default.
- W4210539705 hasConceptScore W4210539705C16930146 @default.
- W4210539705 hasConceptScore W4210539705C170493617 @default.
- W4210539705 hasConceptScore W4210539705C180361614 @default.
- W4210539705 hasConceptScore W4210539705C185592680 @default.
- W4210539705 hasConceptScore W4210539705C2775960820 @default.
- W4210539705 hasConceptScore W4210539705C2779395532 @default.
- W4210539705 hasConceptScore W4210539705C2781294074 @default.
- W4210539705 hasConceptScore W4210539705C2992686903 @default.
- W4210539705 hasConceptScore W4210539705C49892992 @default.
- W4210539705 hasConceptScore W4210539705C55493867 @default.
- W4210539705 hasConceptScore W4210539705C62112901 @default.
- W4210539705 hasConceptScore W4210539705C71924100 @default.
- W4210539705 hasConceptScore W4210539705C86803240 @default.
- W4210539705 hasConceptScore W4210539705C89429830 @default.
- W4210539705 hasConceptScore W4210539705C95444343 @default.
- W4210539705 hasLocation W42105397051 @default.
- W4210539705 hasOpenAccess W4210539705 @default.
- W4210539705 hasPrimaryLocation W42105397051 @default.
- W4210539705 hasRelatedWork W1992731515 @default.
- W4210539705 hasRelatedWork W2001668238 @default.
- W4210539705 hasRelatedWork W2055810659 @default.
- W4210539705 hasRelatedWork W2360893882 @default.
- W4210539705 hasRelatedWork W2369516964 @default.
- W4210539705 hasRelatedWork W2371437420 @default.
- W4210539705 hasRelatedWork W2765685634 @default.
- W4210539705 hasRelatedWork W3154189534 @default.
- W4210539705 hasRelatedWork W339979645 @default.
- W4210539705 hasRelatedWork W4230024640 @default.
- W4210539705 hasVolume "79" @default.
- W4210539705 isParatext "false" @default.
- W4210539705 isRetracted "false" @default.
- W4210539705 workType "article" @default.