Why the study?
Extracellular vesicles regulate pathways like inflammation and angiogenesis with multifaceted roles in atherosclerosis, prompting an examination of their involvement across lesion development phases and the need to standardize isolation procedures.
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Design
Review
Unstandardized EV isolation precludes clinical biomarker use in atherosclerosis now; leaves open cargo-specific studies to extend therapeutic potential.
Extracellular vesicles (EVs) are membrane particles released by most cell types in response to different stimuli. They are composed of a lipid bilayer that encloses a wide range of bioactive material, including proteins and nucleic acids. EVs have garnered increasing attention over recent years, as their role in intercellular communication has been brought to light. As such, they have been found to regulate pathophysiologic pathways like inflammation, angiogenesis, or senescence, and are therefore implicated in key aspects atherosclerosis initiation and progression. Interestingly, EVs appear to have a multifaceted role; depending on their cargo, they can either facilitate or hamper the development of atherosclerotic lesions. In this review, we examine how EVs of varying origins may be implicated in the different phases of atherosclerotic lesion development. We also discuss the need to standardize isolation and analysis procedures to fully fulfil their potential as biomarkers and therapeutics for cardiovascular diseases.
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A 2021 study studied this question.
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