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Can a Peritoneal Conduit Become an Artery?

OBJECTIVE: Current vascular grafts all have limitations. This study examined peritoneum as a potential graft material and the in vivo transfer of peritoneum into a functional artery like conduit after end to end anastomosis into the common carotid artery of sheep. The aim was to investigate whether...

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Autores principales: Davik, Petter, Chabadova, Zuzana, Altreuther, Martin, Leinan, Ingeborg, Bandaru, Sashidar, Akyürek, Levent M., Mattsson, Erney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077027/
https://www.ncbi.nlm.nih.gov/pubmed/33937897
http://dx.doi.org/10.1016/j.ejvsvf.2020.10.001
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author Davik, Petter
Chabadova, Zuzana
Altreuther, Martin
Leinan, Ingeborg
Bandaru, Sashidar
Akyürek, Levent M.
Mattsson, Erney
author_facet Davik, Petter
Chabadova, Zuzana
Altreuther, Martin
Leinan, Ingeborg
Bandaru, Sashidar
Akyürek, Levent M.
Mattsson, Erney
author_sort Davik, Petter
collection PubMed
description OBJECTIVE: Current vascular grafts all have limitations. This study examined peritoneum as a potential graft material and the in vivo transfer of peritoneum into a functional artery like conduit after end to end anastomosis into the common carotid artery of sheep. The aim was to investigate whether implantation of a peritoneal tube into the arterial tree results in a structure with function, histological findings, and gene expression like an artery, and whether such arterialisation occurs through a conversion of the phenotype of peritoneal cells or from host cell migration into the implant. METHODS: Peritoneum with adherent rectus aponeurosis from sheep was used to form tubular vascular grafts that were implanted into the common carotid artery of six sheep, then removed after five months. Two sheep received allogenic peritoneal grafts and four sheep received autologous peritoneal grafts. RESULTS: One sheep died shortly after implantation, so five of the six sheep were followed. Five months after implantation, four of the five remaining grafts were patent. Three of four patent grafts were aneurysmal. The four patent grafts had developed an endothelial layer indistinguishable from that of the adjacent normal artery, and a medial layer with smooth muscle cells with a surrounding adventitia. The new conduit displayed vasomotor function not present at the time of implantation. DNA genotyping showed that the media in the new conduit consisted of recipient smooth muscle cells. Little difference in mRNA expression was demonstrated between the post-implantation conduit and normal artery. CONCLUSION: During a five month implantation period in the arterial system, peritoneum converted into a tissue that histologically and functionally resembled a normal artery, with a functional genetic expression that resembled that of an artery. Single nucleotide polymorphism analysis indicated that this conversion occurs through host cell migration into the graft.
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spelling pubmed-80770272021-04-29 Can a Peritoneal Conduit Become an Artery? Davik, Petter Chabadova, Zuzana Altreuther, Martin Leinan, Ingeborg Bandaru, Sashidar Akyürek, Levent M. Mattsson, Erney EJVES Vasc Forum Original Research OBJECTIVE: Current vascular grafts all have limitations. This study examined peritoneum as a potential graft material and the in vivo transfer of peritoneum into a functional artery like conduit after end to end anastomosis into the common carotid artery of sheep. The aim was to investigate whether implantation of a peritoneal tube into the arterial tree results in a structure with function, histological findings, and gene expression like an artery, and whether such arterialisation occurs through a conversion of the phenotype of peritoneal cells or from host cell migration into the implant. METHODS: Peritoneum with adherent rectus aponeurosis from sheep was used to form tubular vascular grafts that were implanted into the common carotid artery of six sheep, then removed after five months. Two sheep received allogenic peritoneal grafts and four sheep received autologous peritoneal grafts. RESULTS: One sheep died shortly after implantation, so five of the six sheep were followed. Five months after implantation, four of the five remaining grafts were patent. Three of four patent grafts were aneurysmal. The four patent grafts had developed an endothelial layer indistinguishable from that of the adjacent normal artery, and a medial layer with smooth muscle cells with a surrounding adventitia. The new conduit displayed vasomotor function not present at the time of implantation. DNA genotyping showed that the media in the new conduit consisted of recipient smooth muscle cells. Little difference in mRNA expression was demonstrated between the post-implantation conduit and normal artery. CONCLUSION: During a five month implantation period in the arterial system, peritoneum converted into a tissue that histologically and functionally resembled a normal artery, with a functional genetic expression that resembled that of an artery. Single nucleotide polymorphism analysis indicated that this conversion occurs through host cell migration into the graft. Elsevier 2020-10-13 /pmc/articles/PMC8077027/ /pubmed/33937897 http://dx.doi.org/10.1016/j.ejvsvf.2020.10.001 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Davik, Petter
Chabadova, Zuzana
Altreuther, Martin
Leinan, Ingeborg
Bandaru, Sashidar
Akyürek, Levent M.
Mattsson, Erney
Can a Peritoneal Conduit Become an Artery?
title Can a Peritoneal Conduit Become an Artery?
title_full Can a Peritoneal Conduit Become an Artery?
title_fullStr Can a Peritoneal Conduit Become an Artery?
title_full_unstemmed Can a Peritoneal Conduit Become an Artery?
title_short Can a Peritoneal Conduit Become an Artery?
title_sort can a peritoneal conduit become an artery?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077027/
https://www.ncbi.nlm.nih.gov/pubmed/33937897
http://dx.doi.org/10.1016/j.ejvsvf.2020.10.001
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