Endoplasmic Reticulum (ER) Stress-Generated Extracellular Vesicles (Microparticles) Self-Perpetuate ER Stress and Mediate Endothelial Cell Dysfunction Independently of Cell Survival

Aisha Osman; Heba El-Gamal; Mazhar Pasha; Asad Zeidan; Hesham M Korashy; Shahenda S Abdelsalam; Maram Hasan; Tarek Benameur; Abdelali Agouni

doi:10.3389/fcvm.2020.584791

Endoplasmic Reticulum (ER) Stress-Generated Extracellular Vesicles (Microparticles) Self-Perpetuate ER Stress and Mediate Endothelial Cell Dysfunction Independently of Cell Survival

Front Cardiovasc Med. 2020 Dec 10:7:584791. doi: 10.3389/fcvm.2020.584791. eCollection 2020.

Authors

Aisha Osman¹, Heba El-Gamal¹, Mazhar Pasha¹, Asad Zeidan², Hesham M Korashy¹, Shahenda S Abdelsalam¹, Maram Hasan¹, Tarek Benameur³, Abdelali Agouni¹

Affiliations

¹ Department of Pharmaceutical Sciences, College of Pharmacy, QU Health, Qatar University, Doha, Qatar.
² Department of Basic Sciences, College of Medicine, QU Health, Qatar University, Doha, Qatar.
³ College of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia.

Abstract

Circulating extracellular vesicles (EVs) are recognized as biomarkers and effectors of endothelial dysfunction, the initiating step of cardiovascular abnormalities. Among these EVs, microparticles (MPs) are vesicles directly released from the cytoplasmic membrane of activated cells. MPs were shown to induce endothelial dysfunction through the activation of endoplasmic reticulum (ER) stress. However, it is not known whether ER stress can lead to MPs release from endothelial cells and what biological messages are carried by these MPs. Therefore, we aimed to assess the impact of ER stress on MPs shedding from endothelial cells, and to investigate their effects on endothelial cell function. EA.hy926 endothelial cells or human umbilical vein endothelial cells (HUVECs) were treated for 24 h with ER stress inducers, thapsigargin or dithiothreitol (DTT), in the presence or absence of 4-Phenylbutyric acid (PBA), a chemical chaperone to inhibit ER stress. Then, MPs were isolated and used to treat cells (10-20 μg/mL) for 24-48 h before assessing ER stress response, angiogenic capacity, nitric oxide (NO) release, autophagy and apoptosis. ER stress (thapsigargin or DDT)-generated MPs did not differ quantitatively from controls; however, they carried deleterious messages for endothelial function. Exposure of endothelial cells to ER stress-generated MPs increased mRNA and protein expression of key ER stress markers, indicating a vicious circle activation of ER stress. ER stress (thapsigargin)-generated MPs impaired the angiogenic capacity of HUVECs and reduced NO release, indicating an impaired endothelial function. While ER stress (thapsigargin)-generated MPs altered the release of inflammatory cytokines, they did not, however, affect autophagy or apoptosis in HUVECs. This work enhances the general understanding of the deleterious effects carried out by MPs in medical conditions where ER stress is sustainably activated such as diabetes and metabolic syndrome.

Keywords: ER stress; apoptosis; cardiovascular disease; endothelial function (dysfunction); extracellular vesicles (EVs); microparticles (MPs).