Matches in SemOpenAlex for { <https://semopenalex.org/work/W3030795697> ?p ?o ?g. }
- W3030795697 endingPage "116" @default.
- W3030795697 startingPage "103" @default.
- W3030795697 abstract "Surgical reconstruction of tubular esophageal defects with autologous gastrointestinal segments is the gold standard treatment to replace damaged or diseased esophageal tissues. Unfortunately, this approach is associated with adverse complications, including dysphagia, donor-site morbidity, and in some cases patient death. Bilayer silk fibroin (BLSF) scaffolds were investigated as alternative, acellular grafts for tubular esophagoplasty in a porcine defect model for 3 months of implantation. Adult Yucatan mini-swine (n = 5) were subjected to esophageal reconstruction with tubular BLSF grafts (2 cm in length) in combination with transient esophageal stenting for 2 months followed by a 1-month period, where the graft site was unstented. All animals receiving BLSF grafts survived and were capable of solid food consumption, however strictures were noted at graft regions in 60% of the experimental cohort between 2 and 3 months postop and required balloon dilation. In addition, fluoroscopic analysis showed peristaltic function in only 1/5 neotissues. Following swine harvest at 3 months, ex vivo tissue bath evaluations revealed that neoconduits exhibited contractile responses to carbachol, electric field stimulation, and KCl, whereas sodium nitroprusside and isoproterenol induced relaxation effects. Histological (Masson's Trichrome) and immunohistochemical analyses of regenerated tissue conduits showed a stratified, squamous epithelium expressing pan-cytokeratins buttressed by a vascularized lamina propria containing a smooth muscle-rich muscularis mucosa surrounded by a muscularis externa. Neuronal density, characterized by the presence of synaptophysin-positive boutons, was significantly lower in neotissues in comparison to nonsurgical controls. BLSF scaffolds represent a promising platform for the repair of tubular esophageal defects, however improvements in scaffold design are needed to reduce the rate of complications and improve the extent of constructive tissue remodeling. The search for a superior “off-the-shelf” scaffold capable of repairing tubularesophageal defects as well as overcoming limitations associated with conventional autologous gastrointestinal segments remains elusive. The purpose of this study was to investigate the performance of an acellular, bilayer silk fibroin graft (BLSF) for tubular esophagoplasty in a porcine model. Our results demonstrated that BLSF scaffolds supported the formation of tubular neotissues with innervated, vascularized epithelial and muscular components capable of contractile and relaxation responses. BLSF scaffolds represent a promising platform for esophageal tissue engineering." @default.
- W3030795697 created "2020-06-05" @default.
- W3030795697 creator A5006501212 @default.
- W3030795697 creator A5036982100 @default.
- W3030795697 creator A5044506723 @default.
- W3030795697 creator A5055973161 @default.
- W3030795697 creator A5059019540 @default.
- W3030795697 creator A5066354063 @default.
- W3030795697 creator A5083579148 @default.
- W3030795697 creator A5087970204 @default.
- W3030795697 creator A5091171337 @default.
- W3030795697 date "2021-01-01" @default.
- W3030795697 modified "2023-09-26" @default.
- W3030795697 title "Evaluation of Bilayer Silk Fibroin Grafts for Tubular Esophagoplasty in a Porcine Defect Model" @default.
- W3030795697 cites W1927547492 @default.
- W3030795697 cites W1966680459 @default.
- W3030795697 cites W1975978136 @default.
- W3030795697 cites W1993352660 @default.
- W3030795697 cites W1995160097 @default.
- W3030795697 cites W1995686224 @default.
- W3030795697 cites W2004020712 @default.
- W3030795697 cites W2012958126 @default.
- W3030795697 cites W2016844038 @default.
- W3030795697 cites W2035074704 @default.
- W3030795697 cites W2038747440 @default.
- W3030795697 cites W2050530834 @default.
- W3030795697 cites W2051661800 @default.
- W3030795697 cites W2052209313 @default.
- W3030795697 cites W2054244326 @default.
- W3030795697 cites W2073958168 @default.
- W3030795697 cites W2086236274 @default.
- W3030795697 cites W2087724770 @default.
- W3030795697 cites W2094650509 @default.
- W3030795697 cites W2106140402 @default.
- W3030795697 cites W2113958535 @default.
- W3030795697 cites W2141284915 @default.
- W3030795697 cites W2143875551 @default.
- W3030795697 cites W2156775891 @default.
- W3030795697 cites W2158206341 @default.
- W3030795697 cites W2163098312 @default.
- W3030795697 cites W2169386802 @default.
- W3030795697 cites W2292956350 @default.
- W3030795697 cites W2341165979 @default.
- W3030795697 cites W2518855932 @default.
- W3030795697 cites W2538220025 @default.
- W3030795697 cites W2574889600 @default.
- W3030795697 cites W2599810018 @default.
- W3030795697 cites W2757167112 @default.
- W3030795697 cites W2794061088 @default.
- W3030795697 cites W2794433880 @default.
- W3030795697 cites W2886494883 @default.
- W3030795697 cites W2891516625 @default.
- W3030795697 cites W2897723147 @default.
- W3030795697 cites W2916644927 @default.
- W3030795697 cites W2921181776 @default.
- W3030795697 cites W4242688031 @default.
- W3030795697 doi "https://doi.org/10.1089/ten.tea.2020.0061" @default.
- W3030795697 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7826443" @default.
- W3030795697 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32460641" @default.
- W3030795697 hasPublicationYear "2021" @default.
- W3030795697 type Work @default.
- W3030795697 sameAs 3030795697 @default.
- W3030795697 citedByCount "6" @default.
- W3030795697 countsByYear W30307956972021 @default.
- W3030795697 countsByYear W30307956972022 @default.
- W3030795697 countsByYear W30307956972023 @default.
- W3030795697 crossrefType "journal-article" @default.
- W3030795697 hasAuthorship W3030795697A5006501212 @default.
- W3030795697 hasAuthorship W3030795697A5036982100 @default.
- W3030795697 hasAuthorship W3030795697A5044506723 @default.
- W3030795697 hasAuthorship W3030795697A5055973161 @default.
- W3030795697 hasAuthorship W3030795697A5059019540 @default.
- W3030795697 hasAuthorship W3030795697A5066354063 @default.
- W3030795697 hasAuthorship W3030795697A5083579148 @default.
- W3030795697 hasAuthorship W3030795697A5087970204 @default.
- W3030795697 hasAuthorship W3030795697A5091171337 @default.
- W3030795697 hasBestOaLocation W30307956972 @default.
- W3030795697 hasConcept C105702510 @default.
- W3030795697 hasConcept C141071460 @default.
- W3030795697 hasConcept C142724271 @default.
- W3030795697 hasConcept C150903083 @default.
- W3030795697 hasConcept C207001950 @default.
- W3030795697 hasConcept C26291073 @default.
- W3030795697 hasConcept C2777310793 @default.
- W3030795697 hasConcept C2777819096 @default.
- W3030795697 hasConcept C2777960253 @default.
- W3030795697 hasConcept C529295009 @default.
- W3030795697 hasConcept C71924100 @default.
- W3030795697 hasConcept C86803240 @default.
- W3030795697 hasConceptScore W3030795697C105702510 @default.
- W3030795697 hasConceptScore W3030795697C141071460 @default.
- W3030795697 hasConceptScore W3030795697C142724271 @default.
- W3030795697 hasConceptScore W3030795697C150903083 @default.
- W3030795697 hasConceptScore W3030795697C207001950 @default.
- W3030795697 hasConceptScore W3030795697C26291073 @default.
- W3030795697 hasConceptScore W3030795697C2777310793 @default.
- W3030795697 hasConceptScore W3030795697C2777819096 @default.
- W3030795697 hasConceptScore W3030795697C2777960253 @default.