A tissue-engineered model of the atherosclerotic plaque cap

Toward understanding the role of microcalcifications in plaque rupture

Journal Article (2023)
Authors

Imke Jansen (Erasmus MC)

Hanneke Crielaard (Erasmus MC)

T. B. Wissing (Erasmus MC)

Carlijn Bouten (Eindhoven University of Technology)

Frank J. Gijsen (TU Delft - Medical Instruments & Bio-Inspired Technology, Erasmus MC)

AC Akyildiz (TU Delft - Medical Instruments & Bio-Inspired Technology, Erasmus MC)

Eric Farrell (Erasmus MC)

K. van der Heiden (Erasmus MC)

Research Group
Medical Instruments & Bio-Inspired Technology
Copyright
© 2023 Imke Jansen, Hanneke Crielaard, Tamar Wissing, Carlijn Bouten, F.J.H. Gijsen, A.C. Akyildiz, Eric Farrell, Kim van der Heiden
To reference this document use:
https://doi.org/10.1063/5.0168087
More Info
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Publication Year
2023
Language
English
Copyright
© 2023 Imke Jansen, Hanneke Crielaard, Tamar Wissing, Carlijn Bouten, F.J.H. Gijsen, A.C. Akyildiz, Eric Farrell, Kim van der Heiden
Research Group
Medical Instruments & Bio-Inspired Technology
Issue number
3
Volume number
7
DOI:
https://doi.org/10.1063/5.0168087
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Abstract

Rupture of the cap of an atherosclerotic plaque can lead to thrombotic cardiovascular events. It has been suggested, through computational models, that the presence of microcalcifications in the atherosclerotic cap can increase the risk of cap rupture. However, the experimental confirmation of this hypothesis is still lacking. In this study, we have developed a novel tissue-engineered model to mimic the atherosclerotic fibrous cap with microcalcifications and assess the impact of microcalcifications on cap mechanics. First, human carotid plaque caps were analyzed to determine the distribution, size, and density of microcalcifications in real cap tissue. Hydroxyapatite particles with features similar to real cap microcalcifications were used as microcalcification mimics. Injected clusters of hydroxyapatite particles were embedded in a fibrin gel seeded with human myofibroblasts which deposited a native-like collagenous matrix around the particles, during the 21-day culture period. Second harmonic multiphoton microscopy imaging revealed higher local collagen fiber dispersion in regions of hydroxyapatite clusters. Tissue-engineered caps with hydroxyapatite particles demonstrated lower stiffness and ultimate tensile stress than the control group samples under uniaxial tensile loading, suggesting increased rupture risk in atherosclerotic plaques with microcalcifications. This model supports previous computational findings regarding a detrimental role for microcalcifications in cap rupture risk and can further be deployed to elucidate tissue mechanics in pathologies with calcifying soft tissues.