Involvement of Mitochondria in the Selective Response to Microsecond Pulsed Electric Fields on Healthy and Cancer Stem Cells in the Brain
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Published:2024-02-13
Issue:4
Volume:25
Page:2233
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ISSN:1422-0067
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Container-title:International Journal of Molecular Sciences
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language:en
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Short-container-title:IJMS
Author:
Casciati Arianna1ORCID, Taddei Anna Rita2, Rampazzo Elena34, Persano Luca34ORCID, Viola Giampietro34ORCID, Cani Alice34, Bresolin Silvia34, Cesi Vincenzo1, Antonelli Francesca1, Mancuso Mariateresa1ORCID, Merla Caterina1ORCID, Tanori Mirella1ORCID
Affiliation:
1. Division of Health Protection Technologies, Italian National Agency for Energy New Technologies and Sustainable Economic Development (ENEA), Via Anguillarese 301, 00123 Rome, Italy 2. Great Equipment Center-Section of Electron Microscopy, University of Tuscia, Largo dell’Università snc, 01100 Viterbo, Italy 3. Department of Women’s and Children’s Health (SDB), University of Padova, Via Giustiniani 3, 35128 Padova, Italy 4. Pediatric Research Institute (IRP), Corso Stati Uniti 4, 35127 Padova, Italy
Abstract
In the last few years, pulsed electric fields have emerged as promising clinical tools for tumor treatments. This study highlights the distinct impact of a specific pulsed electric field protocol, PEF-5 (0.3 MV/m, 40 μs, 5 pulses), on astrocytes (NHA) and medulloblastoma (D283) and glioblastoma (U87 NS) cancer stem-like cells (CSCs). We pursued this goal by performing ultrastructural analyses corroborated by molecular/omics approaches to understand the vulnerability or resistance mechanisms triggered by PEF-5 exposure in the different cell types. Electron microscopic analyses showed that, independently of exposed cells, the main targets of PEF-5 were the cell membrane and the cytoskeleton, causing membrane filopodium-like protrusion disappearance on the cell surface, here observed for the first time, accompanied by rapid cell swelling. PEF-5 induced different modifications in cell mitochondria. A complete mitochondrial dysfunction was demonstrated in D283, while a mild or negligible perturbation was observed in mitochondria of U87 NS cells and NHAs, respectively, not sufficient to impair their cell functions. Altogether, these results suggest the possibility of using PEF-based technology as a novel strategy to target selectively mitochondria of brain CSCs, preserving healthy cells.
Funder
European Union’s Horizon 2020 research and innovation program Fondazione AIRC per la Ricerca sul Cancro Cassa di Risparmio di Padova e Rovigo (CARIPARO) Foundation Umberto Veronesi Foundation
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