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Tubular organ epithelialisation
Hollow, tubular organs including oesophagus, trachea, stomach, intestine, bladder and urethra may require repair or replacement due to disease. Current treatment is considered an unmet clinical need, and tissue engineering strategies aim to overcome these by fabricating synthetic constructs as tissu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308438/ https://www.ncbi.nlm.nih.gov/pubmed/28228931 http://dx.doi.org/10.1177/2041731416683950 |
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author | Saksena, Rhea Gao, Chuanyu Wicox, Mathew de Mel, Achala |
author_facet | Saksena, Rhea Gao, Chuanyu Wicox, Mathew de Mel, Achala |
author_sort | Saksena, Rhea |
collection | PubMed |
description | Hollow, tubular organs including oesophagus, trachea, stomach, intestine, bladder and urethra may require repair or replacement due to disease. Current treatment is considered an unmet clinical need, and tissue engineering strategies aim to overcome these by fabricating synthetic constructs as tissue replacements. Smart, functionalised synthetic materials can act as a scaffold base of an organ and multiple cell types, including stem cells can be used to repopulate these scaffolds to replace or repair the damaged or diseased organs. Epithelial cells have not yet completely shown to have efficacious cell–scaffold interactions or good functionality in artificial organs, thus limiting the success of tissue-engineered grafts. Epithelial cells play an essential part of respective organs to maintain their function. Without successful epithelialisation, hollow organs are liable to stenosis, collapse, extensive fibrosis and infection that limit patency. It is clear that the source of cells and physicochemical properties of scaffolds determine the successful epithelialisation. This article presents a review of tissue engineering studies on oesophagus, trachea, stomach, small intestine, bladder and urethral constructs conducted to actualise epithelialised grafts. |
format | Online Article Text |
id | pubmed-5308438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-53084382017-02-22 Tubular organ epithelialisation Saksena, Rhea Gao, Chuanyu Wicox, Mathew de Mel, Achala J Tissue Eng Review Hollow, tubular organs including oesophagus, trachea, stomach, intestine, bladder and urethra may require repair or replacement due to disease. Current treatment is considered an unmet clinical need, and tissue engineering strategies aim to overcome these by fabricating synthetic constructs as tissue replacements. Smart, functionalised synthetic materials can act as a scaffold base of an organ and multiple cell types, including stem cells can be used to repopulate these scaffolds to replace or repair the damaged or diseased organs. Epithelial cells have not yet completely shown to have efficacious cell–scaffold interactions or good functionality in artificial organs, thus limiting the success of tissue-engineered grafts. Epithelial cells play an essential part of respective organs to maintain their function. Without successful epithelialisation, hollow organs are liable to stenosis, collapse, extensive fibrosis and infection that limit patency. It is clear that the source of cells and physicochemical properties of scaffolds determine the successful epithelialisation. This article presents a review of tissue engineering studies on oesophagus, trachea, stomach, small intestine, bladder and urethral constructs conducted to actualise epithelialised grafts. SAGE Publications 2016-12-19 /pmc/articles/PMC5308438/ /pubmed/28228931 http://dx.doi.org/10.1177/2041731416683950 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Saksena, Rhea Gao, Chuanyu Wicox, Mathew de Mel, Achala Tubular organ epithelialisation |
title | Tubular organ epithelialisation |
title_full | Tubular organ epithelialisation |
title_fullStr | Tubular organ epithelialisation |
title_full_unstemmed | Tubular organ epithelialisation |
title_short | Tubular organ epithelialisation |
title_sort | tubular organ epithelialisation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308438/ https://www.ncbi.nlm.nih.gov/pubmed/28228931 http://dx.doi.org/10.1177/2041731416683950 |
work_keys_str_mv | AT saksenarhea tubularorganepithelialisation AT gaochuanyu tubularorganepithelialisation AT wicoxmathew tubularorganepithelialisation AT demelachala tubularorganepithelialisation |