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Blood Vessel-Derived Acellular Matrix for Vascular Graft Application
To overcome the issues connected to the use of autologous vascular grafts and artificial materials for reconstruction of small diameter (<6 mm) blood vessels, this study aimed to develop acellular matrix- (AM-) based vascular grafts. Rat iliac arteries were decellularized by a detergent-enzymatic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124812/ https://www.ncbi.nlm.nih.gov/pubmed/25136610 http://dx.doi.org/10.1155/2014/685426 |
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author | Dall'Olmo, Luigi Zanusso, Ilenia Di Liddo, Rosa Chioato, Tatiana Bertalot, Thomas Guidi, Enrica Conconi, Maria Teresa |
author_facet | Dall'Olmo, Luigi Zanusso, Ilenia Di Liddo, Rosa Chioato, Tatiana Bertalot, Thomas Guidi, Enrica Conconi, Maria Teresa |
author_sort | Dall'Olmo, Luigi |
collection | PubMed |
description | To overcome the issues connected to the use of autologous vascular grafts and artificial materials for reconstruction of small diameter (<6 mm) blood vessels, this study aimed to develop acellular matrix- (AM-) based vascular grafts. Rat iliac arteries were decellularized by a detergent-enzymatic treatment, whereas endothelial cells (ECs) were obtained through enzymatic digestion of rat skin followed by immunomagnetic separation of CD31-positive cells. Sixteen female Lewis rats (8 weeks old) received only AM or previously in vitro reendothelialized AM as abdominal aorta interposition grafts (about 1 cm). The detergent-enzymatic treatment completely removed the cellular part of vessels and both MHC class I and class II antigens. One month after surgery, the luminal surface of implanted AMs was partially covered by ECs and several platelets adhered in the areas lacking cell coverage. Intimal hyperplasia, already detected after 1 month, increased at 3 months. On the contrary, all grafts composed by AM and ECs were completely covered at 1 month and their structure was similar to that of native vessels at 3 months. Taken together, our findings show that prostheses composed of AM preseeded with ECs could be a promising approach for the replacement of blood vessels. |
format | Online Article Text |
id | pubmed-4124812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41248122014-08-18 Blood Vessel-Derived Acellular Matrix for Vascular Graft Application Dall'Olmo, Luigi Zanusso, Ilenia Di Liddo, Rosa Chioato, Tatiana Bertalot, Thomas Guidi, Enrica Conconi, Maria Teresa Biomed Res Int Research Article To overcome the issues connected to the use of autologous vascular grafts and artificial materials for reconstruction of small diameter (<6 mm) blood vessels, this study aimed to develop acellular matrix- (AM-) based vascular grafts. Rat iliac arteries were decellularized by a detergent-enzymatic treatment, whereas endothelial cells (ECs) were obtained through enzymatic digestion of rat skin followed by immunomagnetic separation of CD31-positive cells. Sixteen female Lewis rats (8 weeks old) received only AM or previously in vitro reendothelialized AM as abdominal aorta interposition grafts (about 1 cm). The detergent-enzymatic treatment completely removed the cellular part of vessels and both MHC class I and class II antigens. One month after surgery, the luminal surface of implanted AMs was partially covered by ECs and several platelets adhered in the areas lacking cell coverage. Intimal hyperplasia, already detected after 1 month, increased at 3 months. On the contrary, all grafts composed by AM and ECs were completely covered at 1 month and their structure was similar to that of native vessels at 3 months. Taken together, our findings show that prostheses composed of AM preseeded with ECs could be a promising approach for the replacement of blood vessels. Hindawi Publishing Corporation 2014 2014-07-16 /pmc/articles/PMC4124812/ /pubmed/25136610 http://dx.doi.org/10.1155/2014/685426 Text en Copyright © 2014 Luigi Dall'Olmo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Dall'Olmo, Luigi Zanusso, Ilenia Di Liddo, Rosa Chioato, Tatiana Bertalot, Thomas Guidi, Enrica Conconi, Maria Teresa Blood Vessel-Derived Acellular Matrix for Vascular Graft Application |
title | Blood Vessel-Derived Acellular Matrix for Vascular Graft Application |
title_full | Blood Vessel-Derived Acellular Matrix for Vascular Graft Application |
title_fullStr | Blood Vessel-Derived Acellular Matrix for Vascular Graft Application |
title_full_unstemmed | Blood Vessel-Derived Acellular Matrix for Vascular Graft Application |
title_short | Blood Vessel-Derived Acellular Matrix for Vascular Graft Application |
title_sort | blood vessel-derived acellular matrix for vascular graft application |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124812/ https://www.ncbi.nlm.nih.gov/pubmed/25136610 http://dx.doi.org/10.1155/2014/685426 |
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