Resistance to CLnA-induced ferroptosis is acquired in Caco-2 cells upon differentiation

Géraldine Cuvelier, Perrine Vermonden, J. Rousseau, O. Féron, R. Rezsohazy, Y. Larondelle
{"title":"Resistance to CLnA-induced ferroptosis is acquired in Caco-2 cells upon differentiation","authors":"Géraldine Cuvelier, Perrine Vermonden, J. Rousseau, O. Féron, R. Rezsohazy, Y. Larondelle","doi":"10.3389/fceld.2023.1219672","DOIUrl":null,"url":null,"abstract":"In contrast to canonical ferroptosis inducers, highly peroxidable conjugated linolenic acids (CLnA) directly fuel the lipid peroxidation cascade upon their incorporation into membrane phospholipids. Little is known, however, about the cytotoxicity level of CLnAs to normal epithelial cells. Caco-2 cells, derived from colorectal adenocarcinoma, spontaneously differentiate into enterocyte-like cells over a period of 21 days of cell culturing, allowing for graduated phenotypic shift from proliferative, undifferentiated cells to a functional intestinal barrier. We exploited this property to assess the sensitivity of Caco-2 cells to CLnAs at different stages of differentiation. Our results show a significant decrease in CLnA-induced ferroptotic cell death over time. The acquired resistance aligned with decreases in cell proliferation and in the extent of lipid peroxidation, as well as with an increase in the expression of GPX4 upon differentiation. These results highlight that while CLnAs are highly toxic for proliferating cancer cells, differentiated epithelial cells are resistant to CLnA-induced ferroptosis. Therefore, this study gives credential to the therapeutic use of CLnAs as an anticancer strategy and offers a new model study to further investigate the safety of peroxidable fatty acids in differentiated cells.","PeriodicalId":73072,"journal":{"name":"Frontiers in cell death","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in cell death","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fceld.2023.1219672","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In contrast to canonical ferroptosis inducers, highly peroxidable conjugated linolenic acids (CLnA) directly fuel the lipid peroxidation cascade upon their incorporation into membrane phospholipids. Little is known, however, about the cytotoxicity level of CLnAs to normal epithelial cells. Caco-2 cells, derived from colorectal adenocarcinoma, spontaneously differentiate into enterocyte-like cells over a period of 21 days of cell culturing, allowing for graduated phenotypic shift from proliferative, undifferentiated cells to a functional intestinal barrier. We exploited this property to assess the sensitivity of Caco-2 cells to CLnAs at different stages of differentiation. Our results show a significant decrease in CLnA-induced ferroptotic cell death over time. The acquired resistance aligned with decreases in cell proliferation and in the extent of lipid peroxidation, as well as with an increase in the expression of GPX4 upon differentiation. These results highlight that while CLnAs are highly toxic for proliferating cancer cells, differentiated epithelial cells are resistant to CLnA-induced ferroptosis. Therefore, this study gives credential to the therapeutic use of CLnAs as an anticancer strategy and offers a new model study to further investigate the safety of peroxidable fatty acids in differentiated cells.
Caco-2细胞在分化过程中获得了对clna诱导的铁下垂的抗性
与典型的铁下垂诱导剂不同,高过氧化共轭亚麻酸(CLnA)在与膜磷脂结合后直接促进脂质过氧化级联反应。然而,关于clna对正常上皮细胞的细胞毒性水平知之甚少。Caco-2细胞来源于结直肠腺癌,经过21天的细胞培养,可自发分化为肠细胞样细胞,允许从增殖性未分化细胞到功能性肠屏障的逐渐表型转变。我们利用这一特性来评估Caco-2细胞在不同分化阶段对clna的敏感性。我们的研究结果显示,clna诱导的铁致细胞死亡随着时间的推移而显著减少。获得性耐药与细胞增殖减少、脂质过氧化程度降低以及分化时GPX4表达增加一致。这些结果强调,虽然clna对增殖癌细胞具有高毒性,但分化的上皮细胞对clna诱导的铁下垂具有抗性。因此,本研究为clna作为一种抗癌策略的治疗用途提供了证据,并为进一步研究过氧化物脂肪酸在分化细胞中的安全性提供了新的模型研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
文献相关原料
公司名称 产品信息 采购帮参考价格
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信