Krebs cycle derivatives, dimethyl fumarate and itaconate, control metabolic reprogramming in inflammatory human microglia cell line

IF 3.9 3区 生物学 Q2 CELL BIOLOGY Mitochondrion Pub Date : 2024-09-12 DOI:10.1016/j.mito.2024.101966
Moris Sangineto , Martina Ciarnelli , Archana Moola , Vidyasagar Naik Bukke , Tommaso Cassano , Rosanna Villani , Antonino D. Romano , Giuseppe Di Gioia , Carlo Avolio , Gaetano Serviddio
{"title":"Krebs cycle derivatives, dimethyl fumarate and itaconate, control metabolic reprogramming in inflammatory human microglia cell line","authors":"Moris Sangineto ,&nbsp;Martina Ciarnelli ,&nbsp;Archana Moola ,&nbsp;Vidyasagar Naik Bukke ,&nbsp;Tommaso Cassano ,&nbsp;Rosanna Villani ,&nbsp;Antonino D. Romano ,&nbsp;Giuseppe Di Gioia ,&nbsp;Carlo Avolio ,&nbsp;Gaetano Serviddio","doi":"10.1016/j.mito.2024.101966","DOIUrl":null,"url":null,"abstract":"<div><p>Metabolic reprogramming drives inflammatory activity in macrophages, including microglia, with Krebs cycle (KC) intermediates playing a crucial role as signaling molecules. Here, we show that the bioenergetic profile of LPS-activated human microglial<!--> <!-->clone 3 cell line (HMC3) is characterized by high levels of glycolysis and mitochondrial (mt) respiration, and the treatment with KC derivatives, namely dimethyl-fumarate (DMF) and itaconate (ITA), almost restores normal metabolism. However, despite comparable bioenergetic and anti-inflammatory effects, the mt hyper-activity was differentially modulated by DMF and ITA. DMF normalized complex I activity, while ITA dampened both complex I and II hyper-activity counteracting oxidative stress more efficiently.</p></div>","PeriodicalId":18606,"journal":{"name":"Mitochondrion","volume":"79 ","pages":"Article 101966"},"PeriodicalIF":3.9000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1567724924001247/pdfft?md5=6a5becc343b5697d574ecae4cead3197&pid=1-s2.0-S1567724924001247-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mitochondrion","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567724924001247","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Metabolic reprogramming drives inflammatory activity in macrophages, including microglia, with Krebs cycle (KC) intermediates playing a crucial role as signaling molecules. Here, we show that the bioenergetic profile of LPS-activated human microglial clone 3 cell line (HMC3) is characterized by high levels of glycolysis and mitochondrial (mt) respiration, and the treatment with KC derivatives, namely dimethyl-fumarate (DMF) and itaconate (ITA), almost restores normal metabolism. However, despite comparable bioenergetic and anti-inflammatory effects, the mt hyper-activity was differentially modulated by DMF and ITA. DMF normalized complex I activity, while ITA dampened both complex I and II hyper-activity counteracting oxidative stress more efficiently.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
克雷布斯循环衍生物、富马酸二甲酯和伊他康酸能控制炎性人类小胶质细胞系的代谢重编程
代谢重编程驱动着包括小胶质细胞在内的巨噬细胞的炎症活动,其中克雷布斯循环(KC)中间产物作为信号分子发挥着至关重要的作用。在这里,我们发现 LPS 激活的人小胶质细胞克隆 3 细胞系(HMC3)的生物能特征是高水平的糖酵解和线粒体(mt)呼吸,而用 KC 衍生物(即富马酸二甲酯(DMF)和伊他康酸(ITA))处理几乎可以恢复正常代谢。然而,尽管生物能和抗炎效果相当,但 DMF 和 ITA 对 mt 的高活性有不同的调节作用。DMF 使复合体 I 的活性恢复正常,而 ITA 则抑制了复合体 I 和 II 的高活性,从而更有效地对抗氧化应激。
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 去求助
相关文献
Diagnostic utility of ERG immunostaining in dermatofibroma.
IF 3.4 4区 医学Journal of Clinical PathologyPub Date : 2023-08-01 DOI: 10.1136/jclinpath-2022-208158
Yuichi Yamada, Toshio Ichiki, Yosuke Susuki, Yui Yamada-Nozaki, Yuki Tateishi, Masutaka Furue, Yoshinao Oda
来源期刊
Mitochondrion
Mitochondrion 生物-细胞生物学
CiteScore
9.40
自引率
4.50%
发文量
86
审稿时长
13.6 weeks
期刊介绍: Mitochondrion is a definitive, high profile, peer-reviewed international research journal. The scope of Mitochondrion is broad, reporting on basic science of mitochondria from all organisms and from basic research to pathology and clinical aspects of mitochondrial diseases. The journal welcomes original contributions from investigators working in diverse sub-disciplines such as evolution, biophysics, biochemistry, molecular and cell biology, genetics, pharmacology, toxicology, forensic science, programmed cell death, aging, cancer and clinical features of mitochondrial diseases.
期刊最新文献
Editorial Board Drp1 knockdown aggravates obesity-induced cardiac dysfunction and remodeling Inhibition of the expression of TRIM63 alleviates ventilator-induced diaphragmatic dysfunction by modulating the PPARα/PGC-1α pathway The compound XueShuanTong promotes podocyte mitochondrial autophagy via the AMPK/mTOR pathway to alleviate diabetic nephropathy injury Editorial Board
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1