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Decellularized liver scaffolds promote liver regeneration after partial hepatectomy
The resectable liver volume is strictly limited and this reduces the number of patients who may be treated. Recently, “tissue/organ decellularization”, a new approach in bioengineering, has been investigated for its ability to produce a native organ scaffold by removing all the viable cells. Such a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6715632/ https://www.ncbi.nlm.nih.gov/pubmed/31467359 http://dx.doi.org/10.1038/s41598-019-48948-x |
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author | Shimoda, Hirofumi Yagi, Hiroshi Higashi, Hisanobu Tajima, Kazuki Kuroda, Kohei Abe, Yuta Kitago, Minoru Shinoda, Masahiro Kitagawa, Yuko |
author_facet | Shimoda, Hirofumi Yagi, Hiroshi Higashi, Hisanobu Tajima, Kazuki Kuroda, Kohei Abe, Yuta Kitago, Minoru Shinoda, Masahiro Kitagawa, Yuko |
author_sort | Shimoda, Hirofumi |
collection | PubMed |
description | The resectable liver volume is strictly limited and this reduces the number of patients who may be treated. Recently, “tissue/organ decellularization”, a new approach in bioengineering, has been investigated for its ability to produce a native organ scaffold by removing all the viable cells. Such a scaffold may support the repair of damaged or injured tissue. The purpose of this study was to evaluate the potential contribution of liver scaffolds to hepatic regeneration after hepatectomy. We sutured the partial liver scaffolds onto the surfaces of partially hepatectomized porcine livers and assessed their therapeutic potential by immune histological analysis at various time points. Animals were sacrificed after surgery and the implanted scaffolds were evaluated for the infiltration of various types of cells. Immune histochemical study showed that blood vessel-like structures, covered with CD31 positive endothelial cells and ALB positive cells, were present in all parts of the scaffolds at days 10 and 28. Blood inflow was observed in some of these ductal structures. More interestingly, CK19 and EpCAM positive cells appeared at day 10. These results suggest that the implantation of a decellularized organ scaffold could promote structural reorganization after liver resection. |
format | Online Article Text |
id | pubmed-6715632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67156322019-09-13 Decellularized liver scaffolds promote liver regeneration after partial hepatectomy Shimoda, Hirofumi Yagi, Hiroshi Higashi, Hisanobu Tajima, Kazuki Kuroda, Kohei Abe, Yuta Kitago, Minoru Shinoda, Masahiro Kitagawa, Yuko Sci Rep Article The resectable liver volume is strictly limited and this reduces the number of patients who may be treated. Recently, “tissue/organ decellularization”, a new approach in bioengineering, has been investigated for its ability to produce a native organ scaffold by removing all the viable cells. Such a scaffold may support the repair of damaged or injured tissue. The purpose of this study was to evaluate the potential contribution of liver scaffolds to hepatic regeneration after hepatectomy. We sutured the partial liver scaffolds onto the surfaces of partially hepatectomized porcine livers and assessed their therapeutic potential by immune histological analysis at various time points. Animals were sacrificed after surgery and the implanted scaffolds were evaluated for the infiltration of various types of cells. Immune histochemical study showed that blood vessel-like structures, covered with CD31 positive endothelial cells and ALB positive cells, were present in all parts of the scaffolds at days 10 and 28. Blood inflow was observed in some of these ductal structures. More interestingly, CK19 and EpCAM positive cells appeared at day 10. These results suggest that the implantation of a decellularized organ scaffold could promote structural reorganization after liver resection. Nature Publishing Group UK 2019-08-29 /pmc/articles/PMC6715632/ /pubmed/31467359 http://dx.doi.org/10.1038/s41598-019-48948-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shimoda, Hirofumi Yagi, Hiroshi Higashi, Hisanobu Tajima, Kazuki Kuroda, Kohei Abe, Yuta Kitago, Minoru Shinoda, Masahiro Kitagawa, Yuko Decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
title | Decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
title_full | Decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
title_fullStr | Decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
title_full_unstemmed | Decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
title_short | Decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
title_sort | decellularized liver scaffolds promote liver regeneration after partial hepatectomy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6715632/ https://www.ncbi.nlm.nih.gov/pubmed/31467359 http://dx.doi.org/10.1038/s41598-019-48948-x |
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