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Engineered human organ-specific urethra as a functional substitute

Urologic patients may be affected by pathologies requiring surgical reconstruction to re-establish a normal function. The lack of autologous tissues to reconstruct the urethra led clinicians toward new solutions, such as tissue engineering. Tridimensional tissues were produced and characterized from...

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Autores principales: Caneparo, Christophe, Chabaud, Stéphane, Fradette, Julie, Bolduc, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734558/
https://www.ncbi.nlm.nih.gov/pubmed/36494468
http://dx.doi.org/10.1038/s41598-022-25311-1
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author Caneparo, Christophe
Chabaud, Stéphane
Fradette, Julie
Bolduc, Stéphane
author_facet Caneparo, Christophe
Chabaud, Stéphane
Fradette, Julie
Bolduc, Stéphane
author_sort Caneparo, Christophe
collection PubMed
description Urologic patients may be affected by pathologies requiring surgical reconstruction to re-establish a normal function. The lack of autologous tissues to reconstruct the urethra led clinicians toward new solutions, such as tissue engineering. Tridimensional tissues were produced and characterized from a clinical perspective. The balance was optimized between increasing the mechanical resistance of urethral-engineered tissue and preserving the urothelium’s barrier function, essential to avoid urine extravasation and subsequent inflammation and fibrosis. The substitutes produced using a mix of vesical (VF) and dermal fibroblasts (DF) in either 90%:10% or 80%:20% showed mechanical resistance values comparable to human native bladder tissue while maintaining functionality. The presence of mature urothelium markers such as uroplakins and tight junctions were documented. All substitutes showed similar histological features except for the noticeable decrease in polysaccharide globules for the substitutes made with a higher proportion of DF. The degree of maturation evaluated with electron microscopy was positively correlated with the increased concentration of VF in the stroma. Substitutes produced with VF and at least 10% of DF showed sufficient mechanical resistance to withstand surgeon manipulation and high functionality, which may improve long-term patients’ quality of life, representing a great future alternative to current treatments.
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spelling pubmed-97345582022-12-11 Engineered human organ-specific urethra as a functional substitute Caneparo, Christophe Chabaud, Stéphane Fradette, Julie Bolduc, Stéphane Sci Rep Article Urologic patients may be affected by pathologies requiring surgical reconstruction to re-establish a normal function. The lack of autologous tissues to reconstruct the urethra led clinicians toward new solutions, such as tissue engineering. Tridimensional tissues were produced and characterized from a clinical perspective. The balance was optimized between increasing the mechanical resistance of urethral-engineered tissue and preserving the urothelium’s barrier function, essential to avoid urine extravasation and subsequent inflammation and fibrosis. The substitutes produced using a mix of vesical (VF) and dermal fibroblasts (DF) in either 90%:10% or 80%:20% showed mechanical resistance values comparable to human native bladder tissue while maintaining functionality. The presence of mature urothelium markers such as uroplakins and tight junctions were documented. All substitutes showed similar histological features except for the noticeable decrease in polysaccharide globules for the substitutes made with a higher proportion of DF. The degree of maturation evaluated with electron microscopy was positively correlated with the increased concentration of VF in the stroma. Substitutes produced with VF and at least 10% of DF showed sufficient mechanical resistance to withstand surgeon manipulation and high functionality, which may improve long-term patients’ quality of life, representing a great future alternative to current treatments. Nature Publishing Group UK 2022-12-09 /pmc/articles/PMC9734558/ /pubmed/36494468 http://dx.doi.org/10.1038/s41598-022-25311-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Caneparo, Christophe
Chabaud, Stéphane
Fradette, Julie
Bolduc, Stéphane
Engineered human organ-specific urethra as a functional substitute
title Engineered human organ-specific urethra as a functional substitute
title_full Engineered human organ-specific urethra as a functional substitute
title_fullStr Engineered human organ-specific urethra as a functional substitute
title_full_unstemmed Engineered human organ-specific urethra as a functional substitute
title_short Engineered human organ-specific urethra as a functional substitute
title_sort engineered human organ-specific urethra as a functional substitute
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734558/
https://www.ncbi.nlm.nih.gov/pubmed/36494468
http://dx.doi.org/10.1038/s41598-022-25311-1
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