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

Author:

Grossini Elena1ORCID,Esposito Teresa23,Viretto Michela23,Venkatesan Sakthipriyan1ORCID,Licari Ilaria23,Surico Daniela34,Della Corte Francesco23ORCID,Castello Luigi56ORCID,Bruno Stefania7ORCID,Quaglia Marco68,Comi Cristoforo910ORCID,Cantaluppi Vincenzo38ORCID,Vaschetto Rosanna23ORCID

Affiliation:

1. Laboratory of Physiology, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy

2. Anesthesia and Intensive Care, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy

3. Maggiore della Carità Hospital, 28100 Novara, Italy

4. Gynecology and Obstetrics, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy

5. Internal Medicine, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy

6. Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo, 15121 Alessandria, Italy

7. Laboratory of Translational Research, Department of Medical Sciences, University of Torino, 10126 Torino, Italy

8. Nephrology, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy

9. Neurology Unit, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy

10. Sant’Andrea Hospital, 00189 Vercelli, Italy

Abstract

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.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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