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Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration

Introduction: Attempted tracheal replacement efforts thus far have had very little success. Major limiting factors have been the inability to efficiently re-vascularise and mimic the mechanical properties of native tissue. The major objective of this study was to optimise a previously developed coll...

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Autores principales: Khalid, Tehreem, Soriano, Luis, Lemoine, Mark, Cryan, Sally-Ann, O’Brien, Fergal J., O’Leary, Cian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281188/
https://www.ncbi.nlm.nih.gov/pubmed/37346796
http://dx.doi.org/10.3389/fbioe.2023.1187500
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author Khalid, Tehreem
Soriano, Luis
Lemoine, Mark
Cryan, Sally-Ann
O’Brien, Fergal J.
O’Leary, Cian
author_facet Khalid, Tehreem
Soriano, Luis
Lemoine, Mark
Cryan, Sally-Ann
O’Brien, Fergal J.
O’Leary, Cian
author_sort Khalid, Tehreem
collection PubMed
description Introduction: Attempted tracheal replacement efforts thus far have had very little success. Major limiting factors have been the inability to efficiently re-vascularise and mimic the mechanical properties of native tissue. The major objective of this study was to optimise a previously developed collagen-hyaluronic acid scaffold (CHyA-B), which has shown to facilitate the growth of respiratory cells in distinct regions, as a potential tracheal replacement device. Methods: A biodegradable thermoplastic polymer was 3D-printed into different designs and underwent multi-modal mechanical assessment. The 3D-printed constructs were incorporated into the CHyA-B scaffolds and subjected to in vitro and ex vivo vascularisation. Results: The polymeric backbone provided sufficient strength to the CHyA-B scaffold, with yield loads of 1.31–5.17 N/mm and flexural moduli of 0.13–0.26 MPa. Angiogenic growth factor release (VEGF and bFGF) and angiogenic gene upregulation (KDR, TEK-2 and ANG-1) was detected in composite scaffolds and remained sustainable up to 14 days. Confocal microscopy and histological sectioning confirmed the presence of infiltrating blood vessel throughout composite scaffolds both in vitro and ex vivo. Discussion: By addressing both the mechanical and physiological requirements of tracheal scaffolds, this work has begun to pave the way for a new therapeutic option for large tracheal defects.
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spelling pubmed-102811882023-06-21 Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration Khalid, Tehreem Soriano, Luis Lemoine, Mark Cryan, Sally-Ann O’Brien, Fergal J. O’Leary, Cian Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: Attempted tracheal replacement efforts thus far have had very little success. Major limiting factors have been the inability to efficiently re-vascularise and mimic the mechanical properties of native tissue. The major objective of this study was to optimise a previously developed collagen-hyaluronic acid scaffold (CHyA-B), which has shown to facilitate the growth of respiratory cells in distinct regions, as a potential tracheal replacement device. Methods: A biodegradable thermoplastic polymer was 3D-printed into different designs and underwent multi-modal mechanical assessment. The 3D-printed constructs were incorporated into the CHyA-B scaffolds and subjected to in vitro and ex vivo vascularisation. Results: The polymeric backbone provided sufficient strength to the CHyA-B scaffold, with yield loads of 1.31–5.17 N/mm and flexural moduli of 0.13–0.26 MPa. Angiogenic growth factor release (VEGF and bFGF) and angiogenic gene upregulation (KDR, TEK-2 and ANG-1) was detected in composite scaffolds and remained sustainable up to 14 days. Confocal microscopy and histological sectioning confirmed the presence of infiltrating blood vessel throughout composite scaffolds both in vitro and ex vivo. Discussion: By addressing both the mechanical and physiological requirements of tracheal scaffolds, this work has begun to pave the way for a new therapeutic option for large tracheal defects. Frontiers Media S.A. 2023-06-06 /pmc/articles/PMC10281188/ /pubmed/37346796 http://dx.doi.org/10.3389/fbioe.2023.1187500 Text en Copyright © 2023 Khalid, Soriano, Lemoine, Cryan, O’Brien and O’Leary. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Khalid, Tehreem
Soriano, Luis
Lemoine, Mark
Cryan, Sally-Ann
O’Brien, Fergal J.
O’Leary, Cian
Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
title Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
title_full Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
title_fullStr Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
title_full_unstemmed Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
title_short Development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
title_sort development of tissue-engineered tracheal scaffold with refined mechanical properties and vascularisation for tracheal regeneration
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281188/
https://www.ncbi.nlm.nih.gov/pubmed/37346796
http://dx.doi.org/10.3389/fbioe.2023.1187500
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