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Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues

The airway epithelium lining the luminal surface of the respiratory tract creates a protective barrier that ensures maintenance of tissue homeostasis and prevention of respiratory diseases. The airway epithelium, unfortunately, is frequently injured by inhaled toxic materials, trauma, or medical pro...

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Autores principales: Chen, Jiawen, Mir, Seyed Mohammad, Hudock, Maria R., Pinezich, Meghan R., Chen, Panpan, Bacchetta, Matthew, Vunjak-Novakovic, Gordana, Kim, Jinho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIP Publishing LLC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836726/
https://www.ncbi.nlm.nih.gov/pubmed/36644417
http://dx.doi.org/10.1063/5.0123127
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author Chen, Jiawen
Mir, Seyed Mohammad
Hudock, Maria R.
Pinezich, Meghan R.
Chen, Panpan
Bacchetta, Matthew
Vunjak-Novakovic, Gordana
Kim, Jinho
author_facet Chen, Jiawen
Mir, Seyed Mohammad
Hudock, Maria R.
Pinezich, Meghan R.
Chen, Panpan
Bacchetta, Matthew
Vunjak-Novakovic, Gordana
Kim, Jinho
author_sort Chen, Jiawen
collection PubMed
description The airway epithelium lining the luminal surface of the respiratory tract creates a protective barrier that ensures maintenance of tissue homeostasis and prevention of respiratory diseases. The airway epithelium, unfortunately, is frequently injured by inhaled toxic materials, trauma, or medical procedures. Substantial or repeated airway epithelial injury can lead to dysregulated intrinsic repair pathways and aberrant tissue remodeling that can lead to dysfunctional airway epithelium. While disruption in the epithelial integrity is directly linked to degraded epithelial barrier function, the correlation between the structure and function of the airway epithelium remains elusive. In this study, we quantified the impact of acutely induced airway epithelium injury on disruption of the epithelial barrier functions. By monitoring alternation of the flow motions and tissue bioimpedance at local injury site, degradation of the epithelial functions, including mucociliary clearance and tight/adherens junction formation, were accurately determined with a high spatiotemporal resolution. Computational models that can simulate and predict the disruption of the mucociliary flow and airway tissue bioimpedance have been generated to assist interpretation of the experimental results. Collectively, findings of this study advance our knowledge of the structure–function relationships of the airway epithelium that can promote development of efficient and accurate diagnosis of airway tissue injury.
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spelling pubmed-98367262023-01-13 Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues Chen, Jiawen Mir, Seyed Mohammad Hudock, Maria R. Pinezich, Meghan R. Chen, Panpan Bacchetta, Matthew Vunjak-Novakovic, Gordana Kim, Jinho APL Bioeng Articles The airway epithelium lining the luminal surface of the respiratory tract creates a protective barrier that ensures maintenance of tissue homeostasis and prevention of respiratory diseases. The airway epithelium, unfortunately, is frequently injured by inhaled toxic materials, trauma, or medical procedures. Substantial or repeated airway epithelial injury can lead to dysregulated intrinsic repair pathways and aberrant tissue remodeling that can lead to dysfunctional airway epithelium. While disruption in the epithelial integrity is directly linked to degraded epithelial barrier function, the correlation between the structure and function of the airway epithelium remains elusive. In this study, we quantified the impact of acutely induced airway epithelium injury on disruption of the epithelial barrier functions. By monitoring alternation of the flow motions and tissue bioimpedance at local injury site, degradation of the epithelial functions, including mucociliary clearance and tight/adherens junction formation, were accurately determined with a high spatiotemporal resolution. Computational models that can simulate and predict the disruption of the mucociliary flow and airway tissue bioimpedance have been generated to assist interpretation of the experimental results. Collectively, findings of this study advance our knowledge of the structure–function relationships of the airway epithelium that can promote development of efficient and accurate diagnosis of airway tissue injury. AIP Publishing LLC 2023-01-11 /pmc/articles/PMC9836726/ /pubmed/36644417 http://dx.doi.org/10.1063/5.0123127 Text en © 2023 Author(s). https://creativecommons.org/licenses/by/4.0/All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Articles
Chen, Jiawen
Mir, Seyed Mohammad
Hudock, Maria R.
Pinezich, Meghan R.
Chen, Panpan
Bacchetta, Matthew
Vunjak-Novakovic, Gordana
Kim, Jinho
Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
title Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
title_full Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
title_fullStr Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
title_full_unstemmed Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
title_short Opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
title_sort opto-electromechanical quantification of epithelial barrier function in injured and healthy airway tissues
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836726/
https://www.ncbi.nlm.nih.gov/pubmed/36644417
http://dx.doi.org/10.1063/5.0123127
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