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Quantification of cell-bubble interactions in a 3D engineered tissue phantom
Understanding cell-bubble interactions is crucial for preventing bubble related pathologies and harnessing their potential therapeutic benefits. Bubbles can occur in the body as a result of therapeutic intravenous administration, surgery, infections or decompression. Subsequent interactions with liv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524813/ https://www.ncbi.nlm.nih.gov/pubmed/28740100 http://dx.doi.org/10.1038/s41598-017-06678-y |
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author | Walsh, C. Ovenden, N. Stride, E. Cheema, U. |
author_facet | Walsh, C. Ovenden, N. Stride, E. Cheema, U. |
author_sort | Walsh, C. |
collection | PubMed |
description | Understanding cell-bubble interactions is crucial for preventing bubble related pathologies and harnessing their potential therapeutic benefits. Bubbles can occur in the body as a result of therapeutic intravenous administration, surgery, infections or decompression. Subsequent interactions with living cells, may result in pathological responses such as decompression sickness (DCS). This work investigates the interactions that occur between bubbles formed during decompression and cells in a 3D engineered tissue phantom. Increasing the tissue phantoms’ cellular density resulted in decreased dissolved O(2) (DO) concentrations (p = 0.0003) measured using real-time O(2) monitoring. Direct microscopic observation of these phantoms, revealed a significant (p = 0.0024) corresponding reduction in bubble nucleation. No significant difference in growth rate or maximum size of the bubbles was measured (p = 0.99 and 0.23). These results show that bubble nucleation is dominated by DO concentration (affected by cellular metabolism), rather than potential nucleation sites provided by cell-surfaces. Consequent bubble growth depends not only on DO concentration but also on competition for dissolved gas. Cell death was found to significantly increase (p = 0.0116) following a bubble-forming decompression. By comparison to 2D experiments; the more biomimetic 3D geometry and extracellular matrix in this work, provide data more applicable for understanding and developing models of in vivo bubble dynamics. |
format | Online Article Text |
id | pubmed-5524813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55248132017-07-26 Quantification of cell-bubble interactions in a 3D engineered tissue phantom Walsh, C. Ovenden, N. Stride, E. Cheema, U. Sci Rep Article Understanding cell-bubble interactions is crucial for preventing bubble related pathologies and harnessing their potential therapeutic benefits. Bubbles can occur in the body as a result of therapeutic intravenous administration, surgery, infections or decompression. Subsequent interactions with living cells, may result in pathological responses such as decompression sickness (DCS). This work investigates the interactions that occur between bubbles formed during decompression and cells in a 3D engineered tissue phantom. Increasing the tissue phantoms’ cellular density resulted in decreased dissolved O(2) (DO) concentrations (p = 0.0003) measured using real-time O(2) monitoring. Direct microscopic observation of these phantoms, revealed a significant (p = 0.0024) corresponding reduction in bubble nucleation. No significant difference in growth rate or maximum size of the bubbles was measured (p = 0.99 and 0.23). These results show that bubble nucleation is dominated by DO concentration (affected by cellular metabolism), rather than potential nucleation sites provided by cell-surfaces. Consequent bubble growth depends not only on DO concentration but also on competition for dissolved gas. Cell death was found to significantly increase (p = 0.0116) following a bubble-forming decompression. By comparison to 2D experiments; the more biomimetic 3D geometry and extracellular matrix in this work, provide data more applicable for understanding and developing models of in vivo bubble dynamics. Nature Publishing Group UK 2017-07-24 /pmc/articles/PMC5524813/ /pubmed/28740100 http://dx.doi.org/10.1038/s41598-017-06678-y Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Walsh, C. Ovenden, N. Stride, E. Cheema, U. Quantification of cell-bubble interactions in a 3D engineered tissue phantom |
title | Quantification of cell-bubble interactions in a 3D engineered tissue phantom |
title_full | Quantification of cell-bubble interactions in a 3D engineered tissue phantom |
title_fullStr | Quantification of cell-bubble interactions in a 3D engineered tissue phantom |
title_full_unstemmed | Quantification of cell-bubble interactions in a 3D engineered tissue phantom |
title_short | Quantification of cell-bubble interactions in a 3D engineered tissue phantom |
title_sort | quantification of cell-bubble interactions in a 3d engineered tissue phantom |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524813/ https://www.ncbi.nlm.nih.gov/pubmed/28740100 http://dx.doi.org/10.1038/s41598-017-06678-y |
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