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Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells

Iron overload (IO) is associated with cardiovascular diseases, including heart failure. Our study’s aim was to examine the mechanism by which IO triggers cell death in H9c2 cells. IO caused accumulation of intracellular and mitochondrial iron as shown by the use of iron-binding fluorescent reporters...

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Autores principales: Tam, Eddie, Sung, Hye Kyoung, Lam, Nhat Hung, You, Sally, Cho, Sungji, Ahmed, Saher M., Abdul-Sater, Ali A., Sweeney, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818517/
https://www.ncbi.nlm.nih.gov/pubmed/36611912
http://dx.doi.org/10.3390/cells12010118
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author Tam, Eddie
Sung, Hye Kyoung
Lam, Nhat Hung
You, Sally
Cho, Sungji
Ahmed, Saher M.
Abdul-Sater, Ali A.
Sweeney, Gary
author_facet Tam, Eddie
Sung, Hye Kyoung
Lam, Nhat Hung
You, Sally
Cho, Sungji
Ahmed, Saher M.
Abdul-Sater, Ali A.
Sweeney, Gary
author_sort Tam, Eddie
collection PubMed
description Iron overload (IO) is associated with cardiovascular diseases, including heart failure. Our study’s aim was to examine the mechanism by which IO triggers cell death in H9c2 cells. IO caused accumulation of intracellular and mitochondrial iron as shown by the use of iron-binding fluorescent reporters, FerroOrange and MitoFerroFluor. Expression of cytosolic and mitochondrial isoforms of Ferritin was also induced by IO. IO-induced iron accumulation and cellular ROS was rapid and temporally linked. ROS accumulation was detected in the cytosol and mitochondrial compartments with CellROX, DCF-DA and MitoSOX fluorescent dyes and partly reversed by the general antioxidant N-acetyl cysteine or the mitochondrial antioxidant SkQ1. Antioxidants also reduced the downstream activation of apoptosis and lytic cell death quantified by Caspase 3 cleavage/activation, mitochondrial Cytochrome c release, Annexin V/Propidium iodide staining and LDH release of IO-treated cells. Finally, overexpression of MitoNEET, an outer mitochondrial membrane protein involved in the transfer of Fe-S clusters between mitochondrial and cytosol, was observed to lower iron and ROS accumulation in the mitochondria. These alterations were correlated with reduced IO-induced cell death by apoptosis in MitoNEET-overexpressing cells. In conclusion, IO mediates H9c2 cell death by causing mitochondrial iron accumulation and subsequent general and mitochondrial ROS upregulation.
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spelling pubmed-98185172023-01-07 Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells Tam, Eddie Sung, Hye Kyoung Lam, Nhat Hung You, Sally Cho, Sungji Ahmed, Saher M. Abdul-Sater, Ali A. Sweeney, Gary Cells Article Iron overload (IO) is associated with cardiovascular diseases, including heart failure. Our study’s aim was to examine the mechanism by which IO triggers cell death in H9c2 cells. IO caused accumulation of intracellular and mitochondrial iron as shown by the use of iron-binding fluorescent reporters, FerroOrange and MitoFerroFluor. Expression of cytosolic and mitochondrial isoforms of Ferritin was also induced by IO. IO-induced iron accumulation and cellular ROS was rapid and temporally linked. ROS accumulation was detected in the cytosol and mitochondrial compartments with CellROX, DCF-DA and MitoSOX fluorescent dyes and partly reversed by the general antioxidant N-acetyl cysteine or the mitochondrial antioxidant SkQ1. Antioxidants also reduced the downstream activation of apoptosis and lytic cell death quantified by Caspase 3 cleavage/activation, mitochondrial Cytochrome c release, Annexin V/Propidium iodide staining and LDH release of IO-treated cells. Finally, overexpression of MitoNEET, an outer mitochondrial membrane protein involved in the transfer of Fe-S clusters between mitochondrial and cytosol, was observed to lower iron and ROS accumulation in the mitochondria. These alterations were correlated with reduced IO-induced cell death by apoptosis in MitoNEET-overexpressing cells. In conclusion, IO mediates H9c2 cell death by causing mitochondrial iron accumulation and subsequent general and mitochondrial ROS upregulation. MDPI 2022-12-28 /pmc/articles/PMC9818517/ /pubmed/36611912 http://dx.doi.org/10.3390/cells12010118 Text en © 2022 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
Tam, Eddie
Sung, Hye Kyoung
Lam, Nhat Hung
You, Sally
Cho, Sungji
Ahmed, Saher M.
Abdul-Sater, Ali A.
Sweeney, Gary
Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells
title Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells
title_full Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells
title_fullStr Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells
title_full_unstemmed Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells
title_short Role of Mitochondrial Iron Overload in Mediating Cell Death in H9c2 Cells
title_sort role of mitochondrial iron overload in mediating cell death in h9c2 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818517/
https://www.ncbi.nlm.nih.gov/pubmed/36611912
http://dx.doi.org/10.3390/cells12010118
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