<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hannon E</submitter><funding>Great Ormond Street Hospital Childrens Charity</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Rosetrees</funding><pagination>105174</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9547295</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(10)</volume><pubmed_abstract>Decellularization of esophagi from several species for tissue engineering is well described, but successful implantation in animal models of esophageal replacement has been challenging. The purpose of this study was to assess feasibility and applicability of esophageal replacement using decellularized porcine esophageal scaffolds in a new pre-clinical model. Following surgical replacement in rabbits with a vascularizing muscle flap, we observed successful anastomoses of decellularized scaffolds, cues of early neovascularization, and prevention of luminal collapse by the use of biodegradable stents. However, despite the success of the surgical procedure, the long-term survival was limited by the fragility of the animal model. Our results indicate that transplantation of a decellularized por</pubmed_abstract><journal>iScience</journal><pubmed_title>Lessons learned from pre-clinical testing of xenogeneic decellularized esophagi in a rabbit model.</pubmed_title><pmcid>PMC9547295</pmcid><funding_grant_id>M362-F1</funding_grant_id><funding_grant_id>M362</funding_grant_id><funding_grant_id>M553</funding_grant_id><funding_grant_id>MR/R002118/1</funding_grant_id><funding_grant_id>V8520</funding_grant_id><funding_grant_id>NIHR-CS-012-002</funding_grant_id><funding_grant_id>CDF-2017-10-037</funding_grant_id><funding_grant_id>ICA-CDRF-2017-03-053</funding_grant_id><funding_grant_id>V0117</funding_grant_id><pubmed_authors>Eaton S</pubmed_authors><pubmed_authors>Pellegrini M</pubmed_authors><pubmed_authors>Maughan EF</pubmed_authors><pubmed_authors>Lowdell MW</pubmed_authors><pubmed_authors>Phylactopoulos DE</pubmed_authors><pubmed_authors>Scottoni F</pubmed_authors><pubmed_authors>Hutchinson JC</pubmed_authors><pubmed_authors>Urbani L</pubmed_authors><pubmed_authors>Proctor TJ</pubmed_authors><pubmed_authors>Lutman R</pubmed_authors><pubmed_authors>Hannon E</pubmed_authors><pubmed_authors>Bonfanti P</pubmed_authors><pubmed_authors>Butler CR</pubmed_authors><pubmed_authors>Durkin N</pubmed_authors><pubmed_authors>Arthurs OJ</pubmed_authors><pubmed_authors>Shibuya S</pubmed_authors><pubmed_authors>De Coppi P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lessons learned from pre-clinical testing of xenogeneic decellularized esophagi in a rabbit model.</name><description>Decellularization of esophagi from several species for tissue engineering is well described, but successful implantation in animal models of esophageal replacement has been challenging. The purpose of this study was to assess feasibility and applicability of esophageal replacement using decellularized porcine esophageal scaffolds in a new pre-clinical model. Following surgical replacement in rabbits with a vascularizing muscle flap, we observed successful anastomoses of decellularized scaffolds, cues of early neovascularization, and prevention of luminal collapse by the use of biodegradable stents. However, despite the success of the surgical procedure, the long-term survival was limited by the fragility of the animal model. Our results indicate that transplantation of a decellularized por</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-31T16:05:56.279Z</modification><creation>2025-02-19T01:28:13.389Z</creation></dates><accession>S-EPMC9547295</accession><cross_references><pubmed>36217545</pubmed><doi>10.1016/j.isci.2022.105174</doi></cross_references></HashMap>