Page 183 - Read Online
P. 183

Berezin et al. Vessel Plus 2020;4:15                                        Vessel Plus
               DOI: 10.20517/2574-1209.2020.03




               Review                                                                        Open Access


               Endothelial cell-derived extracellular vesicles in
               atherosclerosis: the emerging value for diagnosis,
               risk stratification and prognostication


               Alexander E. Berezin , Alexander A. Berezin 2
                                 1
               1 Internal Medicine Department, State Medical University, Zaporozhye 69035, Ukraine.
               2 Internal Medicine Department, Medical Academy of Post-Graduate Education, Zaporozhye 69096, Ukraine.

               Correspondence to: Prof. Alexander E.  Berezin, Internal Medicine  Department, State Medical University  for Zaporozhye,
               Mayakovsky av., Zaporozhye 69035, Ukraine. E-mail: aeberezin@gmail.com
               How to cite this article: Berezin AE, Berezin AA. Endothelial cell-derived extracellular vesicles in atherosclerosis: the emerging
               value for diagnosis, risk stratification and prognostication. Vessel Plus 2020;4:15.
               http://dx.doi.org/10.20517/2574-1209.2020.03

               Received: 6 Jan 2020    First Decision: 20 Mar 2020    Revised: 23 Mar 2020    Accepted: 14 Apr 2020    Published: 16 Jun 2020
               Science Editor: Narasimham L. Parinandi    Copy Editor: Jing-Wen Zhang    Production Editor: Tian Zhang

               Abstract
               Endothelial cell-derived extracellular vesicles are produced by both activated and apoptotic endothelial cells, and
               play a pivotal role in various physiological conditions such as inflammation, repair, programmed cell death, and
               immune responses. There is a large body of evidence on the dysregulation of synthesis and secretion of several
               types of endothelial cell-derived extracellular vesicles, which can then trigger microvascular inflammation,
               atherosclerotic plaque formation, plaque rupture, thrombosis and endothelial dysfunction. The development of
               atherosclerosis and cardiovascular events is associated with an increased number of apoptotic, endothelial cell-
               derived vesicles and a decrease in activated, endothelial cell-derived vesicles. This review depicts the role of
               endothelial cell-derived extracellular vesicles in the manifestation and progression of atherosclerosis. We also
               discuss the clinical use and benefits of altering the immune phenotypes of extracellular vesicles originating from
               endothelial cells, to function as predictive biomarkers in both asymptomatic and subclinical atherosclerosis.


               Keywords: Atherosclerosis, cardiovascular events, extracellular vesicles, endothelial cells



               INTRODUCTION
               Atherosclerosis remains a leading cause of major cardiovascular events (MACEs) and cardiovascular (CV)
               diseases worldwide. It represents a serious economic burden on the healthcare system and is associated
                                                    [1]
               with high rates of mortality and morbidity . While there has been a steady trend towards decreasing CV
               mortality from conditions associated with atherosclerosis such as stroke and myocardial infarction in

                           © The Author(s) 2020. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


                                                                                                                                                       www.vpjournal.net
   178   179   180   181   182   183   184   185   186   187   188