The interplay of collagen, macrophages, and microcalcification in atherosclerotic plaque cap rupture mechanics

Review (2024)
Authors

Imke Jansen (Erasmus MC)

Rachel Cahalane (National University of Ireland Galway, Harvard Medical School)

Ranmadusha M. Hengst (Erasmus MC)

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

E. Farrell (Erasmus MC)

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

Elena Aikawa (Harvard Medical School)

Kim van der Heiden (Erasmus MC)

Tamar B. Wissing (Erasmus MC)

Research Group
Medical Instruments & Bio-Inspired Technology
Copyright
© 2024 Imke Jansen, Rachel Cahalane, Ranmadusha Hengst, A.C. Akyildiz, Eric Farrell, F.J.H. Gijsen, Elena Aikawa, Kim van der Heiden, Tamar Wissing
To reference this document use:
https://doi.org/10.1007/s00395-024-01033-5
More Info
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Publication Year
2024
Language
English
Copyright
© 2024 Imke Jansen, Rachel Cahalane, Ranmadusha Hengst, A.C. Akyildiz, Eric Farrell, F.J.H. Gijsen, Elena Aikawa, Kim van der Heiden, Tamar Wissing
Research Group
Medical Instruments & Bio-Inspired Technology
Issue number
2
Volume number
119
Pages (from-to)
193-213
DOI:
https://doi.org/10.1007/s00395-024-01033-5
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Abstract

The rupture of an atherosclerotic plaque cap overlying a lipid pool and/or necrotic core can lead to thrombotic cardiovascular events. In essence, the rupture of the plaque cap is a mechanical event, which occurs when the local stress exceeds the local tissue strength. However, due to inter- and intra-cap heterogeneity, the resulting ultimate cap strength varies, causing proper assessment of the plaque at risk of rupture to be lacking. Important players involved in tissue strength include the load-bearing collagenous matrix, macrophages, as major promoters of extracellular matrix degradation, and microcalcifications, deposits that can exacerbate local stress, increasing tissue propensity for rupture. This review summarizes the role of these components individually in tissue mechanics, along with the interplay between them. We argue that to be able to improve risk assessment, a better understanding of the effect of these individual components, as well as their reciprocal relationships on cap mechanics, is required. Finally, we discuss potential future steps, including a holistic multidisciplinary approach, multifactorial 3D in vitro model systems, and advancements in imaging techniques. The obtained knowledge will ultimately serve as input to help diagnose, prevent, and treat atherosclerotic cap rupture.