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A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation

BACKGROUND: We have previously applied in vivo tissue‐engineered vascular grafts constructed in patients’ subcutaneous spaces. However, since the formation of these vascular grafts depends on host health, their application is challenging in patients with suppressed regenerative ability. Therefore, t...

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Autores principales: Yamanami, Masashi, Kanda, Keiichi, Morimoto, Kazuki, Inoue, Tomoya, Watanabe, Taiji, Sakai, Osamu, Kami, Daisuke, Gojo, Satoshi, Yaku, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299228/
https://www.ncbi.nlm.nih.gov/pubmed/34739732
http://dx.doi.org/10.1111/aor.14102
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author Yamanami, Masashi
Kanda, Keiichi
Morimoto, Kazuki
Inoue, Tomoya
Watanabe, Taiji
Sakai, Osamu
Kami, Daisuke
Gojo, Satoshi
Yaku, Hitoshi
author_facet Yamanami, Masashi
Kanda, Keiichi
Morimoto, Kazuki
Inoue, Tomoya
Watanabe, Taiji
Sakai, Osamu
Kami, Daisuke
Gojo, Satoshi
Yaku, Hitoshi
author_sort Yamanami, Masashi
collection PubMed
description BACKGROUND: We have previously applied in vivo tissue‐engineered vascular grafts constructed in patients’ subcutaneous spaces. However, since the formation of these vascular grafts depends on host health, their application is challenging in patients with suppressed regenerative ability. Therefore, the allogeneic implantation of grafts from healthy donors needs to be evaluated. This study aimed to fabricate allogeneic cardiovascular grafts in animals. MATERIALS AND METHODS: Silicone rod molds were implanted into subcutaneous pouches in dogs; the implants, along with surrounding connective tissues, were harvested after four weeks. Tubular connective tissues were decellularized and stored before they were cut open, trimmed to elliptical sheets, and implanted into the common carotid arteries of another dog as vascular patches (n = 6); these were resected and histologically evaluated at 1, 2, and 4 weeks after implantation. RESULTS: No aneurysmal changes were observed by echocardiography. Histologically, we observed neointima formation on the luminal graft surface and graft wall cell infiltration. At 2 and 4 weeks after implantation, α‐SMA‐positive cells were observed in the neointima and graft wall. At 4 weeks after implantation, the endothelial lining was observed at the grafts’ luminal surfaces. CONCLUSION: Our data suggest that decellularized connective tissue membranes can be prepared and stored for later use as allogeneic cardiovascular grafts.
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spelling pubmed-92992282022-07-21 A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation Yamanami, Masashi Kanda, Keiichi Morimoto, Kazuki Inoue, Tomoya Watanabe, Taiji Sakai, Osamu Kami, Daisuke Gojo, Satoshi Yaku, Hitoshi Artif Organs Main Text BACKGROUND: We have previously applied in vivo tissue‐engineered vascular grafts constructed in patients’ subcutaneous spaces. However, since the formation of these vascular grafts depends on host health, their application is challenging in patients with suppressed regenerative ability. Therefore, the allogeneic implantation of grafts from healthy donors needs to be evaluated. This study aimed to fabricate allogeneic cardiovascular grafts in animals. MATERIALS AND METHODS: Silicone rod molds were implanted into subcutaneous pouches in dogs; the implants, along with surrounding connective tissues, were harvested after four weeks. Tubular connective tissues were decellularized and stored before they were cut open, trimmed to elliptical sheets, and implanted into the common carotid arteries of another dog as vascular patches (n = 6); these were resected and histologically evaluated at 1, 2, and 4 weeks after implantation. RESULTS: No aneurysmal changes were observed by echocardiography. Histologically, we observed neointima formation on the luminal graft surface and graft wall cell infiltration. At 2 and 4 weeks after implantation, α‐SMA‐positive cells were observed in the neointima and graft wall. At 4 weeks after implantation, the endothelial lining was observed at the grafts’ luminal surfaces. CONCLUSION: Our data suggest that decellularized connective tissue membranes can be prepared and stored for later use as allogeneic cardiovascular grafts. John Wiley and Sons Inc. 2021-11-12 2022-04 /pmc/articles/PMC9299228/ /pubmed/34739732 http://dx.doi.org/10.1111/aor.14102 Text en © 2021 The Authors. Artificial Organs published by International Center for Artificial Organ and Transplantation (ICAOT) and Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Main Text
Yamanami, Masashi
Kanda, Keiichi
Morimoto, Kazuki
Inoue, Tomoya
Watanabe, Taiji
Sakai, Osamu
Kami, Daisuke
Gojo, Satoshi
Yaku, Hitoshi
A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
title A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
title_full A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
title_fullStr A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
title_full_unstemmed A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
title_short A tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
title_sort tissue‐engineered, decellularized, connective tissue membrane for allogeneic arterial patch implantation
topic Main Text
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299228/
https://www.ncbi.nlm.nih.gov/pubmed/34739732
http://dx.doi.org/10.1111/aor.14102
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