Cargando…
Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome
Intercellular junctions maintain the integrity of the endothelium. We previously found that the adherens and tight junctions between endothelial cells are disrupted by plasma extracellular vesicles from patients with sickle cell disease (especially those with Acute Chest Syndrome). In the current st...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727676/ https://www.ncbi.nlm.nih.gov/pubmed/33255173 http://dx.doi.org/10.3390/ijms21238884 |
_version_ | 1783621112155865088 |
---|---|
author | Gemel, Joanna Mao, Yifan Lapping-Carr, Gabrielle Beyer, Eric C. |
author_facet | Gemel, Joanna Mao, Yifan Lapping-Carr, Gabrielle Beyer, Eric C. |
author_sort | Gemel, Joanna |
collection | PubMed |
description | Intercellular junctions maintain the integrity of the endothelium. We previously found that the adherens and tight junctions between endothelial cells are disrupted by plasma extracellular vesicles from patients with sickle cell disease (especially those with Acute Chest Syndrome). In the current study, we evaluated the effects of these vesicles on endothelial gap junctions. The vesicles from sickle cell patients (isolated during episodes of Acute Chest Syndrome) disrupted gap junction structures earlier and more severely than the other classes of intercellular junctions (as detected by immunofluorescence). These vesicles were much more potent than those isolated at baseline from the same subject. The treatment of endothelial cells with these vesicles led to reduced levels of connexin43 mRNA and protein. These vesicles severely reduced intercellular communication (transfer of microinjected Neurobiotin). Our data suggest a hierarchy of progressive disruption of different intercellular connections between endothelial cells by circulating extracellular vesicles that may contribute to the pathophysiology of the endothelial disturbances in sickle cell disease. |
format | Online Article Text |
id | pubmed-7727676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77276762020-12-11 Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome Gemel, Joanna Mao, Yifan Lapping-Carr, Gabrielle Beyer, Eric C. Int J Mol Sci Article Intercellular junctions maintain the integrity of the endothelium. We previously found that the adherens and tight junctions between endothelial cells are disrupted by plasma extracellular vesicles from patients with sickle cell disease (especially those with Acute Chest Syndrome). In the current study, we evaluated the effects of these vesicles on endothelial gap junctions. The vesicles from sickle cell patients (isolated during episodes of Acute Chest Syndrome) disrupted gap junction structures earlier and more severely than the other classes of intercellular junctions (as detected by immunofluorescence). These vesicles were much more potent than those isolated at baseline from the same subject. The treatment of endothelial cells with these vesicles led to reduced levels of connexin43 mRNA and protein. These vesicles severely reduced intercellular communication (transfer of microinjected Neurobiotin). Our data suggest a hierarchy of progressive disruption of different intercellular connections between endothelial cells by circulating extracellular vesicles that may contribute to the pathophysiology of the endothelial disturbances in sickle cell disease. MDPI 2020-11-24 /pmc/articles/PMC7727676/ /pubmed/33255173 http://dx.doi.org/10.3390/ijms21238884 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gemel, Joanna Mao, Yifan Lapping-Carr, Gabrielle Beyer, Eric C. Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome |
title | Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome |
title_full | Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome |
title_fullStr | Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome |
title_full_unstemmed | Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome |
title_short | Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome |
title_sort | gap junctions between endothelial cells are disrupted by circulating extracellular vesicles from sickle cell patients with acute chest syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727676/ https://www.ncbi.nlm.nih.gov/pubmed/33255173 http://dx.doi.org/10.3390/ijms21238884 |
work_keys_str_mv | AT gemeljoanna gapjunctionsbetweenendothelialcellsaredisruptedbycirculatingextracellularvesiclesfromsicklecellpatientswithacutechestsyndrome AT maoyifan gapjunctionsbetweenendothelialcellsaredisruptedbycirculatingextracellularvesiclesfromsicklecellpatientswithacutechestsyndrome AT lappingcarrgabrielle gapjunctionsbetweenendothelialcellsaredisruptedbycirculatingextracellularvesiclesfromsicklecellpatientswithacutechestsyndrome AT beyerericc gapjunctionsbetweenendothelialcellsaredisruptedbycirculatingextracellularvesiclesfromsicklecellpatientswithacutechestsyndrome |