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Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects

Circulating extracellular vesicles (EVs) may play a pathophysiological role in the onset of complications of subarachnoid hemorrhage (SAH), potentially contributing to the development of vasospasm (VP). In this study, we aimed to characterize circulating EVs in SAH patients and examine their effects...

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Autores principales: Grossini, Elena, Esposito, Teresa, Viretto, Michela, Venkatesan, Sakthipriyan, Licari, Ilaria, Surico, Daniela, Della Corte, Francesco, Castello, Luigi, Bruno, Stefania, Quaglia, Marco, Comi, Cristoforo, Cantaluppi, Vincenzo, Vaschetto, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573706/
https://www.ncbi.nlm.nih.gov/pubmed/37834361
http://dx.doi.org/10.3390/ijms241914913
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author Grossini, Elena
Esposito, Teresa
Viretto, Michela
Venkatesan, Sakthipriyan
Licari, Ilaria
Surico, Daniela
Della Corte, Francesco
Castello, Luigi
Bruno, Stefania
Quaglia, Marco
Comi, Cristoforo
Cantaluppi, Vincenzo
Vaschetto, Rosanna
author_facet Grossini, Elena
Esposito, Teresa
Viretto, Michela
Venkatesan, Sakthipriyan
Licari, Ilaria
Surico, Daniela
Della Corte, Francesco
Castello, Luigi
Bruno, Stefania
Quaglia, Marco
Comi, Cristoforo
Cantaluppi, Vincenzo
Vaschetto, Rosanna
author_sort Grossini, Elena
collection PubMed
description Circulating extracellular vesicles (EVs) may play a pathophysiological role in the onset of complications of subarachnoid hemorrhage (SAH), potentially contributing to the development of vasospasm (VP). In this study, we aimed to characterize circulating EVs in SAH patients and examine their effects on endothelial and smooth muscle cells (SMCs). In a total of 18 SAH patients, 10 with VP (VP), 8 without VP (NVP), and 5 healthy controls (HC), clinical variables were recorded at different time points. EVs isolated from plasma samples were characterized and used to stimulate human vascular endothelial cells (HUVECs) and SMCs. We found that EVs from SAH patients expressed markers of T-lymphocytes and platelets and had a larger size and a higher concentration compared to those from HC. Moreover, EVs from VP patients reduced cell viability and mitochondrial membrane potential in HUVECs and increased oxidants and nitric oxide (NO) release. Furthermore, EVs from SAH patients increased intracellular calcium levels in SMCs. Altogether, our findings reveal an altered pattern of circulating EVs in SAH patients, suggesting their pathogenic role in promoting endothelial damage and enhancing smooth muscle reactivity. These results have significant implications for the use of EVs as potential diagnostic/prognostic markers and therapeutic tools in SAH management.
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spelling pubmed-105737062023-10-14 Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects Grossini, Elena Esposito, Teresa Viretto, Michela Venkatesan, Sakthipriyan Licari, Ilaria Surico, Daniela Della Corte, Francesco Castello, Luigi Bruno, Stefania Quaglia, Marco Comi, Cristoforo Cantaluppi, Vincenzo Vaschetto, Rosanna Int J Mol Sci Article Circulating extracellular vesicles (EVs) may play a pathophysiological role in the onset of complications of subarachnoid hemorrhage (SAH), potentially contributing to the development of vasospasm (VP). In this study, we aimed to characterize circulating EVs in SAH patients and examine their effects on endothelial and smooth muscle cells (SMCs). In a total of 18 SAH patients, 10 with VP (VP), 8 without VP (NVP), and 5 healthy controls (HC), clinical variables were recorded at different time points. EVs isolated from plasma samples were characterized and used to stimulate human vascular endothelial cells (HUVECs) and SMCs. We found that EVs from SAH patients expressed markers of T-lymphocytes and platelets and had a larger size and a higher concentration compared to those from HC. Moreover, EVs from VP patients reduced cell viability and mitochondrial membrane potential in HUVECs and increased oxidants and nitric oxide (NO) release. Furthermore, EVs from SAH patients increased intracellular calcium levels in SMCs. Altogether, our findings reveal an altered pattern of circulating EVs in SAH patients, suggesting their pathogenic role in promoting endothelial damage and enhancing smooth muscle reactivity. These results have significant implications for the use of EVs as potential diagnostic/prognostic markers and therapeutic tools in SAH management. MDPI 2023-10-05 /pmc/articles/PMC10573706/ /pubmed/37834361 http://dx.doi.org/10.3390/ijms241914913 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Grossini, Elena
Esposito, Teresa
Viretto, Michela
Venkatesan, Sakthipriyan
Licari, Ilaria
Surico, Daniela
Della Corte, Francesco
Castello, Luigi
Bruno, Stefania
Quaglia, Marco
Comi, Cristoforo
Cantaluppi, Vincenzo
Vaschetto, Rosanna
Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects
title Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects
title_full Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects
title_fullStr Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects
title_full_unstemmed Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects
title_short Circulating Extracellular Vesicles in Subarachnoid Hemorrhage Patients: Characterization and Cellular Effects
title_sort circulating extracellular vesicles in subarachnoid hemorrhage patients: characterization and cellular effects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573706/
https://www.ncbi.nlm.nih.gov/pubmed/37834361
http://dx.doi.org/10.3390/ijms241914913
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