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Endothelial cell apoptosis and the role of endothelial cell-derived extracellular vesicles in the progression of atherosclerosis

  • Stephanie Paone
  • Amy A. Baxter
  • Mark D. Hulett
  • Ivan K. H. PoonEmail author
Review
  • 260 Downloads

Abstract

To maintain physiological homeostasis, cell turnover occurs every day in the body via a form of programmed cell death called apoptosis. During apoptosis, cells undergo distinct morphological changes culminating in the disassembly of the dying cell into smaller fragments known as apoptotic bodies (ApoBDs). Dysregulation of apoptosis is associated with diseases including infection, cancer and atherosclerosis. Although the development of atherosclerosis is largely attributed to the accumulation of lipids and inflammatory debris in vessel walls, it is also associated with apoptosis of macrophages, smooth muscle cells (SMCs) and endothelial cells. During cellular activation and apoptosis, endothelial cells can release several types of membrane-bound extracellular vesicles (EVs) including exosomes, microvesicles (MVs)/microparticles and ApoBDs. Emerging evidence in the field suggests that these endothelial cell-derived EVs (EndoEVs) can contribute to intercellular communication during the development of atherosclerosis via the transfer of cellular contents such as protein and microRNA, which may prevent or promote disease progression depending on the context. This review provides an up-to-date overview of the known causes and consequences of endothelial cell death during atherosclerosis along with highlighting current methodological approaches to studying EndoEVs and the potential roles of EndoEVs in atherosclerosis development.

Keywords

Apoptotic bodies Apoptotic cell disassembly Atherosclerosis Endothelial cells Extracellular vesicles Microparticles Microvesicles 

Notes

Funding

This work was supported by grants from the National Health and Medical Research Council of Australia (GNT1125033) to I.K.H.P. and (GNT1141732) to A.A.B., and Australian Research Council (DP170103790) to I.K.H.P.

Compliance with ethical standards

Conflict of interest

The authors declare that they do not have anything to disclose.

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Copyright information

© Springer Nature Switzerland AG 2018

Authors and Affiliations

  • Stephanie Paone
    • 1
  • Amy A. Baxter
    • 1
  • Mark D. Hulett
    • 1
  • Ivan K. H. Poon
    • 1
    Email author
  1. 1.Department of Biochemistry and Genetics, La Trobe Institute for Molecular ScienceLa Trobe UniversityMelbourneAustralia

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