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Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2020 Nov 24; Vol. 21 (23). Date of Electronic Publication: 2020 Nov 24. - Publication Year :
- 2020
-
Abstract
- 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.
- Subjects :
- Acute Chest Syndrome complications
Acute Chest Syndrome pathology
Adolescent
Adult
Anemia, Sickle Cell complications
Anemia, Sickle Cell pathology
Animals
Cell Communication genetics
Child
Child, Preschool
Endothelial Cells metabolism
Endothelium metabolism
Endothelium pathology
Female
Gap Junctions genetics
Humans
Intercellular Junctions genetics
Male
Young Adult
Acute Chest Syndrome genetics
Anemia, Sickle Cell genetics
Connexin 43 genetics
Extracellular Vesicles genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 21
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 33255173
- Full Text :
- https://doi.org/10.3390/ijms21238884