Abstract

We previously found that the plasma of patients with sickle cell disease (SCD) contains large numbers of small extracellular vesicles (EVs) and that the EVs disrupt the integrity of endothelial cell monolayers (especially if obtained during episodes of acute chest syndrome, ACS). The present study was designed to test the generality of this finding to other complications of SCD, specifically to evaluate the possibility that circulating EVs isolated during a vaso-occlusive crises (VOC) also cause damage to the intercellular connections between endothelial cells. Plasma was obtained from nine pediatric subjects at baseline and during VOC episodes. EVs isolated from these samples were added to cultures of microvascular endothelial cells. Immunofluorescence microscopy was employed to assess monolayer integrity and to localize two intercellular junction proteins (VE-cadherin and connexin43). The EVs isolated during VOC caused significantly greater monolayer disruption than those isolated at baseline. The extent of disruption varied between different episodes of VOC or ACS in the same patient. The VOC EVs disrupted the integrity of both junction proteins at appositional membranes. These results suggest that circulating EVs may be involved in modulating endothelial integrity contributing to the pathogenesis of different complications of SCD.

Highlights

  • In addition to plasma proteins and blood cells, the blood contains extracellular vesicles (EVs)

  • We have presented several experiments that extend our previous studies implicating EVs circulating in the plasma of subjects with sickle cell disease (SCD) in vascular complications of that disease

  • We previously showed that subjects with SCD contain an increased abundance of EVs in their plasma that have multiple characteristics consistent with exosomes [31,32]

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Summary

Introduction

In addition to plasma proteins and blood cells, the blood contains extracellular vesicles (EVs). EVs are produced by many kinds of cells. They contain cellular contents, surrounded by lipid bilayers. Large EVs (800 nm–5 μm) are produced by plasma membrane disintegration during apoptosis. Exosomes are generated by release from the endosomal sorting complex required for transport (ESCRT) [2,7,8]. These small EVs contain various proteins related to the ESCRT (Alix, TSG101, HSC70, and HSP90β). They contain tetraspanins (including CD63, CD9, and CD81) and nucleic acids (including DNA, mRNAs, and miRNAs) [9]. EVs from many sources eventually enter the bloodstream

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