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Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture

A significant amount of vascular thrombotic events are associated with rupture of the fibrous cap that overlie atherosclerotic plaques. Cap rupture is however difficult to predict due to the heterogenous composition of the plaque, unknown material properties, and the stochastic nature of the event....

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Autores principales: Wissing, T. B., Van der Heiden, K., Serra, S. M., Smits, A. I. P. M., Bouten, C. V. C., Gijsen, F. J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971478/
https://www.ncbi.nlm.nih.gov/pubmed/35361847
http://dx.doi.org/10.1038/s41598-022-08425-4
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author Wissing, T. B.
Van der Heiden, K.
Serra, S. M.
Smits, A. I. P. M.
Bouten, C. V. C.
Gijsen, F. J. H.
author_facet Wissing, T. B.
Van der Heiden, K.
Serra, S. M.
Smits, A. I. P. M.
Bouten, C. V. C.
Gijsen, F. J. H.
author_sort Wissing, T. B.
collection PubMed
description A significant amount of vascular thrombotic events are associated with rupture of the fibrous cap that overlie atherosclerotic plaques. Cap rupture is however difficult to predict due to the heterogenous composition of the plaque, unknown material properties, and the stochastic nature of the event. Here, we aim to create tissue engineered human fibrous cap models with a variable but controllable collagen composition, suitable for mechanical testing, to scrutinize the reciprocal relationships between composition and mechanical properties. Myofibroblasts were cultured in 1 × 1.5 cm-sized fibrin-based constrained gels for 21 days according to established (dynamic) culture protocols (i.e. static, intermittent or continuous loading) to vary collagen composition (e.g. amount, type and organization). At day 7, a soft 2 mm ∅ fibrin inclusion was introduced in the centre of each tissue to mimic the soft lipid core, simulating the heterogeneity of a plaque. Results demonstrate reproducible collagenous tissues, that mimic the bulk mechanical properties of human caps and vary in collagen composition due to the presence of a successfully integrated soft inclusion and the culture protocol applied. The models can be deployed to assess tissue mechanics, evolution and failure of fibrous caps or complex heterogeneous tissues in general.
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spelling pubmed-89714782022-04-05 Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture Wissing, T. B. Van der Heiden, K. Serra, S. M. Smits, A. I. P. M. Bouten, C. V. C. Gijsen, F. J. H. Sci Rep Article A significant amount of vascular thrombotic events are associated with rupture of the fibrous cap that overlie atherosclerotic plaques. Cap rupture is however difficult to predict due to the heterogenous composition of the plaque, unknown material properties, and the stochastic nature of the event. Here, we aim to create tissue engineered human fibrous cap models with a variable but controllable collagen composition, suitable for mechanical testing, to scrutinize the reciprocal relationships between composition and mechanical properties. Myofibroblasts were cultured in 1 × 1.5 cm-sized fibrin-based constrained gels for 21 days according to established (dynamic) culture protocols (i.e. static, intermittent or continuous loading) to vary collagen composition (e.g. amount, type and organization). At day 7, a soft 2 mm ∅ fibrin inclusion was introduced in the centre of each tissue to mimic the soft lipid core, simulating the heterogeneity of a plaque. Results demonstrate reproducible collagenous tissues, that mimic the bulk mechanical properties of human caps and vary in collagen composition due to the presence of a successfully integrated soft inclusion and the culture protocol applied. The models can be deployed to assess tissue mechanics, evolution and failure of fibrous caps or complex heterogeneous tissues in general. Nature Publishing Group UK 2022-03-31 /pmc/articles/PMC8971478/ /pubmed/35361847 http://dx.doi.org/10.1038/s41598-022-08425-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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/) .
spellingShingle Article
Wissing, T. B.
Van der Heiden, K.
Serra, S. M.
Smits, A. I. P. M.
Bouten, C. V. C.
Gijsen, F. J. H.
Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
title Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
title_full Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
title_fullStr Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
title_full_unstemmed Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
title_short Tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
title_sort tissue-engineered collagenous fibrous cap models to systematically elucidate atherosclerotic plaque rupture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971478/
https://www.ncbi.nlm.nih.gov/pubmed/35361847
http://dx.doi.org/10.1038/s41598-022-08425-4
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