Exploring NLRP3-related phenotypic fingerprints in human macrophages using Cell Painting assay

IF 4.1 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES iScience Pub Date : 2025-03-21 Epub Date: 2025-02-05 DOI:10.1016/j.isci.2025.111961
Matthew Herring , Eva Särndahl , Oleksandr Kotlyar , Nikolai Scherbak , Magnus Engwall , Roger Karlsson , Mikael Ejdebäck , Alexander Persson , Andi Alijagic
{"title":"Exploring NLRP3-related phenotypic fingerprints in human macrophages using Cell Painting assay","authors":"Matthew Herring ,&nbsp;Eva Särndahl ,&nbsp;Oleksandr Kotlyar ,&nbsp;Nikolai Scherbak ,&nbsp;Magnus Engwall ,&nbsp;Roger Karlsson ,&nbsp;Mikael Ejdebäck ,&nbsp;Alexander Persson ,&nbsp;Andi Alijagic","doi":"10.1016/j.isci.2025.111961","DOIUrl":null,"url":null,"abstract":"<div><div>Existing research has proven difficult to understand the interplay between upstream signaling events during NLRP3 inflammasome activation. Additionally, events downstream of inflammasome complex formation such as cytokine release and pyroptosis can exhibit variation, further complicating matters. Cell Painting has emerged as a prominent tool for unbiased evaluation of the effect of perturbations on cell morphological phenotypes. Using this technique, phenotypic fingerprints can be generated that reveal connections between phenotypes and possible modes of action. To the best of our knowledge, this was the first study that utilized Cell Painting on human THP-1 macrophages to generate phenotypic fingerprints in response to different endogenous and exogenous NLRP3 inflammasome triggers and to identify phenotypic features specific to NLRP3 inflammasome complex formation. Our results demonstrated that not only can Cell Painting generate morphological fingerprints that are NLRP3 trigger-specific but it can also identify cellular fingerprints associated with NLRP3 inflammasome activation.</div></div>","PeriodicalId":342,"journal":{"name":"iScience","volume":"28 3","pages":"Article 111961"},"PeriodicalIF":4.1000,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"iScience","FirstCategoryId":"103","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589004225002214","RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Existing research has proven difficult to understand the interplay between upstream signaling events during NLRP3 inflammasome activation. Additionally, events downstream of inflammasome complex formation such as cytokine release and pyroptosis can exhibit variation, further complicating matters. Cell Painting has emerged as a prominent tool for unbiased evaluation of the effect of perturbations on cell morphological phenotypes. Using this technique, phenotypic fingerprints can be generated that reveal connections between phenotypes and possible modes of action. To the best of our knowledge, this was the first study that utilized Cell Painting on human THP-1 macrophages to generate phenotypic fingerprints in response to different endogenous and exogenous NLRP3 inflammasome triggers and to identify phenotypic features specific to NLRP3 inflammasome complex formation. Our results demonstrated that not only can Cell Painting generate morphological fingerprints that are NLRP3 trigger-specific but it can also identify cellular fingerprints associated with NLRP3 inflammasome activation.

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
利用细胞彩绘法探索人巨噬细胞nlrp3相关表型指纹图谱
现有的研究已经证明很难理解NLRP3炎性体激活过程中上游信号事件之间的相互作用。此外,炎性小体形成的下游事件,如细胞因子释放和焦亡,可能表现出变化,进一步使问题复杂化。细胞绘画已经成为一个突出的工具,对扰动对细胞形态表型的影响进行公正的评估。使用这种技术,可以产生表型指纹,揭示表型和可能的作用模式之间的联系。据我们所知,这是第一次利用细胞绘画技术在人THP-1巨噬细胞上生成表型指纹,以响应不同内源性和外源性NLRP3炎性小体触发因素,并鉴定NLRP3炎性小体复合物形成的特异性表型特征。我们的研究结果表明,Cell Painting不仅可以生成NLRP3触发特异性的形态指纹,还可以识别与NLRP3炎性体激活相关的细胞指纹。
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
来源期刊
iScience
iScience Multidisciplinary-Multidisciplinary
CiteScore
7.20
自引率
1.70%
发文量
1972
审稿时长
6 weeks
期刊介绍: Science has many big remaining questions. To address them, we will need to work collaboratively and across disciplines. The goal of iScience is to help fuel that type of interdisciplinary thinking. iScience is a new open-access journal from Cell Press that provides a platform for original research in the life, physical, and earth sciences. The primary criterion for publication in iScience is a significant contribution to a relevant field combined with robust results and underlying methodology. The advances appearing in iScience include both fundamental and applied investigations across this interdisciplinary range of topic areas. To support transparency in scientific investigation, we are happy to consider replication studies and papers that describe negative results. We know you want your work to be published quickly and to be widely visible within your community and beyond. With the strong international reputation of Cell Press behind it, publication in iScience will help your work garner the attention and recognition it merits. Like all Cell Press journals, iScience prioritizes rapid publication. Our editorial team pays special attention to high-quality author service and to efficient, clear-cut decisions based on the information available within the manuscript. iScience taps into the expertise across Cell Press journals and selected partners to inform our editorial decisions and help publish your science in a timely and seamless way.
期刊最新文献
Daily nocturnal homing reveals goal-directed navigation in a wild teleost The effect of Staphylococcus aureus on the persistence of Pseudomonas aeruginosa due to aggregation in cystic fibrosis airway infections A key role for the exoribonuclease XRN1 in regulating the hepatitis B viral transcriptome Construction and validation of a preimplantation kinship identification model using ultra-low-depth whole genome sequencing Multimodal atlas of single neuron metabolic electrophysiological coupling uncovers circadian rewiring
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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