Nanosecond Pulsed Electric Fields (nsPEFs) Modulate Electron Transport in the Plasma Membrane and the Mitochondria.

Complex I Electron Transport System (ETS) Glycolysis Hormesis Oxidative Phosphorylation (OxPhos) Oxygen Consumption Reactive Oxygen Species Redox Homeostasis WST-8 tetrazolium dye trans Plasma Membrane Electron Transport (tPMET)

Journal

Bioelectrochemistry (Amsterdam, Netherlands)
ISSN: 1878-562X
Titre abrégé: Bioelectrochemistry
Pays: Netherlands
ID NLM: 100953583

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 11 07 2023
revised: 05 09 2023
accepted: 08 09 2023
medline: 27 11 2023
pubmed: 23 9 2023
entrez: 22 9 2023
Statut: ppublish

Résumé

Nanosecond pulsed electric fields (nsPEFs) are a pulsed power technology known for ablating tumors, but they also modulate diverse biological mechanisms. Here we show that nsPEFs regulate trans-plasma membrane electron transport (tPMET) rates in the plasma membrane redox system (PMRS) shown as a reduction of the cell-impermeable, WST-8 tetrazolium dye. At lower charging conditions, nsPEFs enhance, and at higher charging conditions inhibit tPMET in H9c2 non-cancerous cardiac myoblasts and 4T1-luc breast cancer cells. This biphasic nsPEF-induced modulation of tPMET is typical of a hormetic stimulus that is beneficial and stress-adaptive at lower levels and damaging at higher levels. NsPEFs also attenuated mitochondrial electron transport system (ETS) activity (O2 consumption) at Complex I when coupled and uncoupled to oxidative phosphorylation. NsPEFs generated more reactive oxygen species (ROS) in mitochondria (mROS) than in the cytosol (cROS) in non-cancer H9c2 heart cells but more cROS than mROS in 4T1-luc cancer cells. Under lower charging conditions, nsPEFs support glycolysis while under higher charging conditions, nsPEFs inhibit electron transport in the PMRS and the mitochondrial ETS producing ROS, ultimately causing cell death. The impact of nsPEF on ETS presents a new paradigm for considering nsPEF modulation of redox functions, including redox homeostasis and metabolism.

Identifiants

pubmed: 37738861
pii: S1567-5394(23)00205-0
doi: 10.1016/j.bioelechem.2023.108568
pii:
doi:

Substances chimiques

Reactive Oxygen Species 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108568

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

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.

Auteurs

Kamal Asadipour (K)

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk Virginia, USA; Department of Electrical and Computer Engineering, Old Dominion University, Norfolk Virginia, USA.

Maisoun Bani Hani (MB)

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk Virginia, USA.

Lucas Potter (L)

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk Virginia, USA; Department of Electrical and Computer Engineering, Old Dominion University, Norfolk Virginia, USA.

Brittney L Ruedlinger (BL)

Department of Biomedical Sciences, Old Dominion University, Norfolk Virginia, USA.

Nicola Lai (N)

Department of Electrical and Computer Engineering, Old Dominion University, Norfolk Virginia, USA.

Stephen J Beebe (SJ)

Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk Virginia, USA. Electronic address: sbeebe@odu.edu.

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Classifications MeSH