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Zinc transporter ZIP7 is a novel determinant of ferroptosis

Ferroptosis is a newly described form of regulated cell death triggered by oxidative stresses and characterized by extensive lipid peroxidation and membrane damages. The name of ferroptosis indicates that the ferroptotic death process depends on iron, but not other metals, as one of its canonical fe...

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Autores principales: Chen, Po-Han, Wu, Jianli, Xu, Yitong, Ding, Chien-Kuang Cornelia, Mestre, Alexander A., Lin, Chao-Chieh, Yang, Wen-Hsuan, Chi, Jen-Tsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895949/
https://www.ncbi.nlm.nih.gov/pubmed/33608508
http://dx.doi.org/10.1038/s41419-021-03482-5
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author Chen, Po-Han
Wu, Jianli
Xu, Yitong
Ding, Chien-Kuang Cornelia
Mestre, Alexander A.
Lin, Chao-Chieh
Yang, Wen-Hsuan
Chi, Jen-Tsan
author_facet Chen, Po-Han
Wu, Jianli
Xu, Yitong
Ding, Chien-Kuang Cornelia
Mestre, Alexander A.
Lin, Chao-Chieh
Yang, Wen-Hsuan
Chi, Jen-Tsan
author_sort Chen, Po-Han
collection PubMed
description Ferroptosis is a newly described form of regulated cell death triggered by oxidative stresses and characterized by extensive lipid peroxidation and membrane damages. The name of ferroptosis indicates that the ferroptotic death process depends on iron, but not other metals, as one of its canonical features. Here, we reported that zinc is also essential for ferroptosis in breast and renal cancer cells. Zinc chelator suppressed ferroptosis, and zinc addition promoted ferroptosis, even during iron chelation. By interrogating zinc-related genes in a genome-wide RNAi screen of ferroptosis, we identified SLC39A7, encoding ZIP7 that controls zinc transport from endoplasmic reticulum (ER) to cytosol, as a novel genetic determinant of ferroptosis. Genetic and chemical inhibition of the ZIP7 protected cells against ferroptosis, and the ferroptosis protection upon ZIP7 knockdown can be abolished by zinc supplementation. We found that the genetic and chemical inhibition of ZIP7 triggered ER stresses, including the induction of the expression of HERPUD1 and ATF3. Importantly, the knockdown of HERPUD1 abolished the ferroptosis protection phenotypes of ZIP7 inhibition. Together, we have uncovered an unexpected role of ZIP7 in ferroptosis by maintaining ER homeostasis. These findings may have therapeutic implications for human diseases involving ferroptosis and zinc dysregulations.
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spelling pubmed-78959492021-03-03 Zinc transporter ZIP7 is a novel determinant of ferroptosis Chen, Po-Han Wu, Jianli Xu, Yitong Ding, Chien-Kuang Cornelia Mestre, Alexander A. Lin, Chao-Chieh Yang, Wen-Hsuan Chi, Jen-Tsan Cell Death Dis Article Ferroptosis is a newly described form of regulated cell death triggered by oxidative stresses and characterized by extensive lipid peroxidation and membrane damages. The name of ferroptosis indicates that the ferroptotic death process depends on iron, but not other metals, as one of its canonical features. Here, we reported that zinc is also essential for ferroptosis in breast and renal cancer cells. Zinc chelator suppressed ferroptosis, and zinc addition promoted ferroptosis, even during iron chelation. By interrogating zinc-related genes in a genome-wide RNAi screen of ferroptosis, we identified SLC39A7, encoding ZIP7 that controls zinc transport from endoplasmic reticulum (ER) to cytosol, as a novel genetic determinant of ferroptosis. Genetic and chemical inhibition of the ZIP7 protected cells against ferroptosis, and the ferroptosis protection upon ZIP7 knockdown can be abolished by zinc supplementation. We found that the genetic and chemical inhibition of ZIP7 triggered ER stresses, including the induction of the expression of HERPUD1 and ATF3. Importantly, the knockdown of HERPUD1 abolished the ferroptosis protection phenotypes of ZIP7 inhibition. Together, we have uncovered an unexpected role of ZIP7 in ferroptosis by maintaining ER homeostasis. These findings may have therapeutic implications for human diseases involving ferroptosis and zinc dysregulations. Nature Publishing Group UK 2021-02-19 /pmc/articles/PMC7895949/ /pubmed/33608508 http://dx.doi.org/10.1038/s41419-021-03482-5 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Po-Han
Wu, Jianli
Xu, Yitong
Ding, Chien-Kuang Cornelia
Mestre, Alexander A.
Lin, Chao-Chieh
Yang, Wen-Hsuan
Chi, Jen-Tsan
Zinc transporter ZIP7 is a novel determinant of ferroptosis
title Zinc transporter ZIP7 is a novel determinant of ferroptosis
title_full Zinc transporter ZIP7 is a novel determinant of ferroptosis
title_fullStr Zinc transporter ZIP7 is a novel determinant of ferroptosis
title_full_unstemmed Zinc transporter ZIP7 is a novel determinant of ferroptosis
title_short Zinc transporter ZIP7 is a novel determinant of ferroptosis
title_sort zinc transporter zip7 is a novel determinant of ferroptosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895949/
https://www.ncbi.nlm.nih.gov/pubmed/33608508
http://dx.doi.org/10.1038/s41419-021-03482-5
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