[Quercetin suppresses pyroptosis in mouse fibroblasts by inhibiting the NLRP3/caspase-1/GSDMD pathway].

Q3 Medicine
P Shu, M Yuan, K Yang, W He, L Liu
{"title":"[Quercetin suppresses pyroptosis in mouse fibroblasts by inhibiting the NLRP3/caspase-1/GSDMD pathway].","authors":"P Shu, M Yuan, K Yang, W He, L Liu","doi":"10.12122/j.issn.1673-4254.2024.10.05","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate whether quercetin inhibits pyroptosis of mouse fibroblast NIH-3T3 cells by regulating the NLRP3/caspase-1/GSDMD signaling pathway.</p><p><strong>Methods: </strong>NIH-3T3 cells were treated with quercetin or MCC950 (a specific inhibitor of NLRP3) before stimulation with lipopolysaccharide (LPS) and ATP to induce cell pyroptosis. The optimal quercetin concentration and duration were screened using the CCK-8assay after testing various concentrations and times. Morphological changes of the treated cells was observed, and the levels of IL-18 and IL-1β in the cell culture supernatant were detected with ELISA; the protein expressions of NLRP3, cleaved caspase-1, and GSDMD-N and the mRNA levels of NLRP3, caspase-1 and GSDMD were detected using Western blotting and qRT-PCR. The changes in cell pyroptosis were examined with TUNEL staining and LDH release assay.</p><p><strong>Results: </strong>The CCK-8 assay indicated that 24-hour treatment with 20 μmol/L quercetin yielded the most favorable results. LPS and ATP stimulation of NIH-3T3 cells induced obvious swelling, cell membrane rupture and leakage of cell contents, significantly increased IL-18 and IL-1β levels, and enhanced protein expressions of NLRP3, cleaved caspase-1 and GSDMD-N and mRNA levels of NLRP3, caspase-1 and GSDMD. LPS and ATP stimulation also caused a significant increment of TUNEL-positive cell counts and LDH release in NIH-3T3 cells. Treatment with quercetin or MCC950 significantly reduced cell pyroptosis induced by LPS and ATP, lowered the concentrations of IL-18 and IL-1β, decreased the expression levels of NLRP3, caspase-1/cleaved caspase-1, GSDMD/GSDMD-N, and reduced the number of TUNEL-positive cells and LDH release.</p><p><strong>Conclusion: </strong>Quercetin suppresses pyroptosis of mouse fibroblasts stimulated with LPS and ATP and reduces secretion of inflammatory cytokines by inhibiting the NLRP3/caspase-1/GSDMD pathway.</p>","PeriodicalId":18962,"journal":{"name":"南方医科大学学报杂志","volume":"44 10","pages":"1874-1880"},"PeriodicalIF":0.0000,"publicationDate":"2024-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11526465/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"南方医科大学学报杂志","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12122/j.issn.1673-4254.2024.10.05","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To investigate whether quercetin inhibits pyroptosis of mouse fibroblast NIH-3T3 cells by regulating the NLRP3/caspase-1/GSDMD signaling pathway.

Methods: NIH-3T3 cells were treated with quercetin or MCC950 (a specific inhibitor of NLRP3) before stimulation with lipopolysaccharide (LPS) and ATP to induce cell pyroptosis. The optimal quercetin concentration and duration were screened using the CCK-8assay after testing various concentrations and times. Morphological changes of the treated cells was observed, and the levels of IL-18 and IL-1β in the cell culture supernatant were detected with ELISA; the protein expressions of NLRP3, cleaved caspase-1, and GSDMD-N and the mRNA levels of NLRP3, caspase-1 and GSDMD were detected using Western blotting and qRT-PCR. The changes in cell pyroptosis were examined with TUNEL staining and LDH release assay.

Results: The CCK-8 assay indicated that 24-hour treatment with 20 μmol/L quercetin yielded the most favorable results. LPS and ATP stimulation of NIH-3T3 cells induced obvious swelling, cell membrane rupture and leakage of cell contents, significantly increased IL-18 and IL-1β levels, and enhanced protein expressions of NLRP3, cleaved caspase-1 and GSDMD-N and mRNA levels of NLRP3, caspase-1 and GSDMD. LPS and ATP stimulation also caused a significant increment of TUNEL-positive cell counts and LDH release in NIH-3T3 cells. Treatment with quercetin or MCC950 significantly reduced cell pyroptosis induced by LPS and ATP, lowered the concentrations of IL-18 and IL-1β, decreased the expression levels of NLRP3, caspase-1/cleaved caspase-1, GSDMD/GSDMD-N, and reduced the number of TUNEL-positive cells and LDH release.

Conclusion: Quercetin suppresses pyroptosis of mouse fibroblasts stimulated with LPS and ATP and reduces secretion of inflammatory cytokines by inhibiting the NLRP3/caspase-1/GSDMD pathway.

[槲皮素通过抑制 NLRP3/caspase-1/GSDMD途径抑制小鼠成纤维细胞的脓毒症】。]
目的研究槲皮素是否能通过调节NLRP3/caspase-1/GSDMD信号通路抑制小鼠成纤维细胞NIH-3T3的热休克:方法:在用脂多糖(LPS)和ATP刺激NIH-3T3细胞诱导其热休克之前,先用槲皮素或MCC950(NLRP3的特异性抑制剂)处理NIH-3T3细胞。在测试了不同的浓度和时间后,使用 CCK-8 分析法筛选出了最佳的槲皮素浓度和持续时间。通过ELISA检测细胞培养上清液中IL-18和IL-1β的水平;通过Western印迹和qRT-PCR检测NLRP3、caspase-1和GSDMD-N的蛋白表达以及NLRP3、caspase-1和GSDMD的mRNA水平。通过 TUNEL 染色和 LDH 释放检测细胞热解的变化:结果:CCK-8 检测表明,20 μmol/L 槲皮素 24 小时处理的结果最理想。LPS和ATP刺激NIH-3T3细胞可引起细胞明显肿胀、细胞膜破裂和细胞内容物渗出,IL-18和IL-1β水平显著升高,NLRP3、裂解的caspase-1和GSDMD-N的蛋白表达以及NLRP3、caspase-1和GSDMD的mRNA水平升高。LPS 和 ATP 刺激也会使 NIH-3T3 细胞中的 TUNEL 阳性细胞数量和 LDH 释放量显著增加。用槲皮素或MCC950处理可明显降低LPS和ATP诱导的细胞热解,降低IL-18和IL-1β的浓度,降低NLRP3、caspase-1/cleaved caspase-1、GSDMD/GSDMD-N的表达水平,减少TUNEL阳性细胞数量和LDH释放:结论:槲皮素通过抑制NLRP3/caspase-1/GSDMD通路,抑制了小鼠成纤维细胞在LPS和ATP刺激下的热凋亡,并减少了炎症细胞因子的分泌。
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
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
208
期刊介绍:
×
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