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Therapeutic potential of astrocyte-derived extracellular vesicles in mitigating cytotoxicity and transcriptome changes in human brain endothelial cells.

Authors :
Stewart R
Hope Hutson K
Nestorova GG
Source :
Neuroscience [Neuroscience] 2024 Nov 12; Vol. 560, pp. 181-190. Date of Electronic Publication: 2024 Sep 27.
Publication Year :
2024

Abstract

This study investigates the therapeutic effect of astrocyte-derived extracellular vesicles (EVs) in mitigating neurotoxicity-induced transcriptome changes, mitochondrial function, and base excision repair mechanisms in human brain endothelial cells (HBECs). Neurodegenerative disorders are marked by inflammatory processes impacting the blood-brain barrier (BBB) that involve its main components- HBECs and astrocytes. Astrocytes maintain homeostasis through various mechanisms, including EV release. The effect of these EVs on mitigating neurotoxicity in HBECs has not been investigated. This study assesses the impact of astrocyte-derived EVs on global transcriptome changes, cell proliferation, cytotoxicity, oxidative DNA damage, and mitochondrial morphology in HBECs exposed to the neurotoxic reagent Na <subscript>2</subscript> Cr <subscript>2</subscript> O <subscript>7</subscript> . Exposure to Na <subscript>2</subscript> Cr <subscript>2</subscript> O <subscript>7</subscript> for 5 and 16 h induced oxidative DNA damage, measured by an increase in genomic 8OHdG, while the EVs reduced the accumulation of the adduct. A neurotoxic environment caused a non-statistically significant upregulation of the DNA repair enzyme OGG1 while the addition of astrocyte-derived EVs was associated with the same level of expression. EVs caused increased cell proliferation and reduced cytotoxicity in Na <subscript>2</subscript> Cr <subscript>2</subscript> O <subscript>7</subscript> -treated cells. Mitochondrial dysfunction associated with a reduced copy number and circular morphology induced by neurotoxic exposure was not reversed by astrocyte-derived EVs. High-throughput RNA sequencing revealed that exposure to Na <subscript>2</subscript> Cr <subscript>2</subscript> O <subscript>7</subscript> suppressed immune response genes. The addition of astrocyte-derived EVs resulted in the dysregulation of long noncoding RNAs impacting genes associated with brain development and angiogenesis. These findings reveal the positive impact of astrocytes-derived EVs in mitigating neurotoxicity and as potential therapeutic avenues for neurodegenerative diseases.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 International Brain Research Organization (IBRO). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-7544
Volume :
560
Database :
MEDLINE
Journal :
Neuroscience
Publication Type :
Academic Journal
Accession number :
39343159
Full Text :
https://doi.org/10.1016/j.neuroscience.2024.09.040