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Mechanical Regulation of Oral Epithelial Barrier Function
Epithelial cell function is modulated by mechanical forces imparted by the extracellular environment. The transmission of forces onto the cytoskeleton by modalities such as mechanical stress and matrix stiffness is necessary to address by the development of new experimental models that permit finely...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10215350/ https://www.ncbi.nlm.nih.gov/pubmed/37237587 http://dx.doi.org/10.3390/bioengineering10050517 |
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author | Lee, Eun-Jin Kim, Yoontae Salipante, Paul Kotula, Anthony P. Lipshutz, Sophie Graves, Dana T. Alimperti, Stella |
author_facet | Lee, Eun-Jin Kim, Yoontae Salipante, Paul Kotula, Anthony P. Lipshutz, Sophie Graves, Dana T. Alimperti, Stella |
author_sort | Lee, Eun-Jin |
collection | PubMed |
description | Epithelial cell function is modulated by mechanical forces imparted by the extracellular environment. The transmission of forces onto the cytoskeleton by modalities such as mechanical stress and matrix stiffness is necessary to address by the development of new experimental models that permit finely tuned cell mechanical challenges. Herein, we developed an epithelial tissue culture model, named the 3D Oral Epi-mucosa platform, to investigate the role mechanical cues in the epithelial barrier. In this platform, low-level mechanical stress (0.1 kPa) is applied to oral keratinocytes, which lie on 3D fibrous collagen (Col) gels whose stiffness is modulated by different concentrations or the addition of other factors such as fibronectin (FN). Our results show that cells lying on intermediate Col (3 mg/mL; stiffness = 30 Pa) demonstrated lower epithelial leakiness compared with soft Col (1.5 mg/mL; stiffness = 10 Pa) and stiff Col (6 mg/mL; stiffness = 120 Pa) gels, indicating that stiffness modulates barrier function. In addition, the presence of FN reversed the barrier integrity by inhibiting the interepithelial interaction via E-cadherin and Zonula occludens-1. Overall, the 3D Oral Epi-mucosa platform, as a new in vitro system, will be utilized to identify new mechanisms and develop future targets involved in mucosal diseases. |
format | Online Article Text |
id | pubmed-10215350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102153502023-05-27 Mechanical Regulation of Oral Epithelial Barrier Function Lee, Eun-Jin Kim, Yoontae Salipante, Paul Kotula, Anthony P. Lipshutz, Sophie Graves, Dana T. Alimperti, Stella Bioengineering (Basel) Article Epithelial cell function is modulated by mechanical forces imparted by the extracellular environment. The transmission of forces onto the cytoskeleton by modalities such as mechanical stress and matrix stiffness is necessary to address by the development of new experimental models that permit finely tuned cell mechanical challenges. Herein, we developed an epithelial tissue culture model, named the 3D Oral Epi-mucosa platform, to investigate the role mechanical cues in the epithelial barrier. In this platform, low-level mechanical stress (0.1 kPa) is applied to oral keratinocytes, which lie on 3D fibrous collagen (Col) gels whose stiffness is modulated by different concentrations or the addition of other factors such as fibronectin (FN). Our results show that cells lying on intermediate Col (3 mg/mL; stiffness = 30 Pa) demonstrated lower epithelial leakiness compared with soft Col (1.5 mg/mL; stiffness = 10 Pa) and stiff Col (6 mg/mL; stiffness = 120 Pa) gels, indicating that stiffness modulates barrier function. In addition, the presence of FN reversed the barrier integrity by inhibiting the interepithelial interaction via E-cadherin and Zonula occludens-1. Overall, the 3D Oral Epi-mucosa platform, as a new in vitro system, will be utilized to identify new mechanisms and develop future targets involved in mucosal diseases. MDPI 2023-04-25 /pmc/articles/PMC10215350/ /pubmed/37237587 http://dx.doi.org/10.3390/bioengineering10050517 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lee, Eun-Jin Kim, Yoontae Salipante, Paul Kotula, Anthony P. Lipshutz, Sophie Graves, Dana T. Alimperti, Stella Mechanical Regulation of Oral Epithelial Barrier Function |
title | Mechanical Regulation of Oral Epithelial Barrier Function |
title_full | Mechanical Regulation of Oral Epithelial Barrier Function |
title_fullStr | Mechanical Regulation of Oral Epithelial Barrier Function |
title_full_unstemmed | Mechanical Regulation of Oral Epithelial Barrier Function |
title_short | Mechanical Regulation of Oral Epithelial Barrier Function |
title_sort | mechanical regulation of oral epithelial barrier function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10215350/ https://www.ncbi.nlm.nih.gov/pubmed/37237587 http://dx.doi.org/10.3390/bioengineering10050517 |
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