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SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis

BACKGROUND: Capsular fibrosis (CF) is the most common long-term complication in implant-based breast augmentation. It is well accepted that the foreign body response (FBR) instigates the development of fibrotic disease. Our study aims to compare murine and human samples of CF and describe the cellul...

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Autores principales: Kuehlmann, Britta, Zucal, Isabel, Bonham, Clark Andrew, Joubert, Lydia-Marie, Prantl, Lukas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091552/
https://www.ncbi.nlm.nih.gov/pubmed/33941075
http://dx.doi.org/10.1186/s12860-021-00364-8
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author Kuehlmann, Britta
Zucal, Isabel
Bonham, Clark Andrew
Joubert, Lydia-Marie
Prantl, Lukas
author_facet Kuehlmann, Britta
Zucal, Isabel
Bonham, Clark Andrew
Joubert, Lydia-Marie
Prantl, Lukas
author_sort Kuehlmann, Britta
collection PubMed
description BACKGROUND: Capsular fibrosis (CF) is the most common long-term complication in implant-based breast augmentation. It is well accepted that the foreign body response (FBR) instigates the development of fibrotic disease. Our study aims to compare murine and human samples of CF and describe the cellular and extracellular matrix (ECM) composition using scanning and transmission electron microscopy (SEM and TEM). RESULTS: Miniature microtextured silicone breast implants were implanted in mice and subsequently harvested at days 15, 30, and 90 post-operation. Isolated human capsules with the most aggravated form of CF (Baker IV) were harvested post-operation. Both were analyzed with SEM and TEM to assess cellular infiltration and ECM structure. An architectural shift of collagen fiber arrangement from unidirectional to multidirectional was observed at day 90 when compared to days 15 and 30. Fibrosis was observed with an increase of histiocytic infiltration. Moreover, bacterial accumulation was seen around silicone fragments. These findings were common in both murine and human capsules. CONCLUSIONS: This murine model accurately recapitulates CF found in humans and can be utilized for future research on cellular invasion in capsular fibrosis. This descriptive study helps to gain a better understanding of cellular mechanisms involved in the FBR. Increases of ECM and cellularity were observed over time with SEM and TEM analysis.
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spelling pubmed-80915522021-05-04 SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis Kuehlmann, Britta Zucal, Isabel Bonham, Clark Andrew Joubert, Lydia-Marie Prantl, Lukas BMC Mol Cell Biol Methodology Article BACKGROUND: Capsular fibrosis (CF) is the most common long-term complication in implant-based breast augmentation. It is well accepted that the foreign body response (FBR) instigates the development of fibrotic disease. Our study aims to compare murine and human samples of CF and describe the cellular and extracellular matrix (ECM) composition using scanning and transmission electron microscopy (SEM and TEM). RESULTS: Miniature microtextured silicone breast implants were implanted in mice and subsequently harvested at days 15, 30, and 90 post-operation. Isolated human capsules with the most aggravated form of CF (Baker IV) were harvested post-operation. Both were analyzed with SEM and TEM to assess cellular infiltration and ECM structure. An architectural shift of collagen fiber arrangement from unidirectional to multidirectional was observed at day 90 when compared to days 15 and 30. Fibrosis was observed with an increase of histiocytic infiltration. Moreover, bacterial accumulation was seen around silicone fragments. These findings were common in both murine and human capsules. CONCLUSIONS: This murine model accurately recapitulates CF found in humans and can be utilized for future research on cellular invasion in capsular fibrosis. This descriptive study helps to gain a better understanding of cellular mechanisms involved in the FBR. Increases of ECM and cellularity were observed over time with SEM and TEM analysis. BioMed Central 2021-05-03 /pmc/articles/PMC8091552/ /pubmed/33941075 http://dx.doi.org/10.1186/s12860-021-00364-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Kuehlmann, Britta
Zucal, Isabel
Bonham, Clark Andrew
Joubert, Lydia-Marie
Prantl, Lukas
SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
title SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
title_full SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
title_fullStr SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
title_full_unstemmed SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
title_short SEM and TEM for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
title_sort sem and tem for identification of capsular fibrosis and cellular behavior around breast implants – a descriptive analysis
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091552/
https://www.ncbi.nlm.nih.gov/pubmed/33941075
http://dx.doi.org/10.1186/s12860-021-00364-8
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