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Iron metabolism mediates microglia susceptibility in ferroptosis
Ferroptosis is implicated in a range of brain disorders, but it is unknown whether neurons or glia in the brain are particularly effected. Here, we report that primary cortical astrocytes (PA), microglia (PM), and neurons (PN) varied in their sensitivities to ferroptosis. Specifically, PM were the m...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469838/ https://www.ncbi.nlm.nih.gov/pubmed/36111246 http://dx.doi.org/10.3389/fncel.2022.995084 |
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author | Jiao, Lingling Li, Xiaolan Luo, Yuxiang Wei, Junfen Ding, Xulong Xiong, Huan Liu, Xuesong Lei, Peng |
author_facet | Jiao, Lingling Li, Xiaolan Luo, Yuxiang Wei, Junfen Ding, Xulong Xiong, Huan Liu, Xuesong Lei, Peng |
author_sort | Jiao, Lingling |
collection | PubMed |
description | Ferroptosis is implicated in a range of brain disorders, but it is unknown whether neurons or glia in the brain are particularly effected. Here, we report that primary cortical astrocytes (PA), microglia (PM), and neurons (PN) varied in their sensitivities to ferroptosis. Specifically, PM were the most sensitive to ferroptosis, while PN were relatively insensitive. In contrast, PN and PM were equally susceptible to apoptosis, with PA being less affected, whereas all three cell types were similarly susceptible to autophagic cell death. In the tri-culture system containing PA, PM, and PN, the cells were more resistant to ferroptosis than that in the monoculture. These results demonstrated that brain cells exhibit different sensitivities under ferroptosis stress and the difference may be explained by the differentially regulated iron metabolism and the ability to handle iron. Continued elucidation of the cell death patterns of neurons and glia will provide a theoretical basis for related strategies to inhibit the death of brain cells. |
format | Online Article Text |
id | pubmed-9469838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94698382022-09-14 Iron metabolism mediates microglia susceptibility in ferroptosis Jiao, Lingling Li, Xiaolan Luo, Yuxiang Wei, Junfen Ding, Xulong Xiong, Huan Liu, Xuesong Lei, Peng Front Cell Neurosci Neuroscience Ferroptosis is implicated in a range of brain disorders, but it is unknown whether neurons or glia in the brain are particularly effected. Here, we report that primary cortical astrocytes (PA), microglia (PM), and neurons (PN) varied in their sensitivities to ferroptosis. Specifically, PM were the most sensitive to ferroptosis, while PN were relatively insensitive. In contrast, PN and PM were equally susceptible to apoptosis, with PA being less affected, whereas all three cell types were similarly susceptible to autophagic cell death. In the tri-culture system containing PA, PM, and PN, the cells were more resistant to ferroptosis than that in the monoculture. These results demonstrated that brain cells exhibit different sensitivities under ferroptosis stress and the difference may be explained by the differentially regulated iron metabolism and the ability to handle iron. Continued elucidation of the cell death patterns of neurons and glia will provide a theoretical basis for related strategies to inhibit the death of brain cells. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9469838/ /pubmed/36111246 http://dx.doi.org/10.3389/fncel.2022.995084 Text en Copyright © 2022 Jiao, Li, Luo, Wei, Ding, Xiong, Liu and Lei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Jiao, Lingling Li, Xiaolan Luo, Yuxiang Wei, Junfen Ding, Xulong Xiong, Huan Liu, Xuesong Lei, Peng Iron metabolism mediates microglia susceptibility in ferroptosis |
title | Iron metabolism mediates microglia susceptibility in ferroptosis |
title_full | Iron metabolism mediates microglia susceptibility in ferroptosis |
title_fullStr | Iron metabolism mediates microglia susceptibility in ferroptosis |
title_full_unstemmed | Iron metabolism mediates microglia susceptibility in ferroptosis |
title_short | Iron metabolism mediates microglia susceptibility in ferroptosis |
title_sort | iron metabolism mediates microglia susceptibility in ferroptosis |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469838/ https://www.ncbi.nlm.nih.gov/pubmed/36111246 http://dx.doi.org/10.3389/fncel.2022.995084 |
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