[Neutrophil extracellular traps extrusion from neutrophils stably adhered to ICAM-1 by lipoteichoic acid stimulation].

Q4 Medicine
Jiaqi Huang, Jinhua Fang, Zhiwei Wu, Jianhua Wu, Ying Fang, Jiangguo Lin
{"title":"[Neutrophil extracellular traps extrusion from neutrophils stably adhered to ICAM-1 by lipoteichoic acid stimulation].","authors":"Jiaqi Huang, Jinhua Fang, Zhiwei Wu, Jianhua Wu, Ying Fang, Jiangguo Lin","doi":"10.7507/1001-5515.202401062","DOIUrl":null,"url":null,"abstract":"<p><p>The effect of neutrophil extracellular traps (NETs) on promoting intravascular microthrombi formation and exacerbating the severity of sepsis in patients has gained extensive attention. However, in sepsis, the mechanisms and key signaling molecules mediating NET formation during direct interactions of endothelial cells and neutrophils still need further explored. Herein, we utilized lipoteichoic acid (LTA), a component shared by Gram-positive bacteria, to induce NET extrusion from neutrophils firmly adhered to the glass slides coated with intercellular adhesion molecule-1(ICAM-1). We also used Sytox green to label NET-DNA and Flou-4 AM as the intracellular Ca <sup>2+</sup> signaling indicator to observe the NET formation and fluctuation of Ca <sup>2+</sup> signaling. Our results illustrated that LTA was able to induce NET release from neutrophils firmly attached to ICAM-1-coated glass slides, and the process was time-dependent. In addition, our study indicated that LTA-induced NET release by neutrophils stably adhered to ICAM-1 depended on Ca <sup>2+</sup> signaling but not intracellular reactive oxygen species (ROS). This study reveals NET formation mediated by direct interactions between endothelial ICAM-1 and neutrophils under LTA stimulation and key signaling molecules involved, providing the theoretical basis for medicine development and clinical treatment for related diseases.</p>","PeriodicalId":39324,"journal":{"name":"生物医学工程学杂志","volume":"41 2","pages":"304-312"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11058506/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"生物医学工程学杂志","FirstCategoryId":"1087","ListUrlMain":"https://doi.org/10.7507/1001-5515.202401062","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The effect of neutrophil extracellular traps (NETs) on promoting intravascular microthrombi formation and exacerbating the severity of sepsis in patients has gained extensive attention. However, in sepsis, the mechanisms and key signaling molecules mediating NET formation during direct interactions of endothelial cells and neutrophils still need further explored. Herein, we utilized lipoteichoic acid (LTA), a component shared by Gram-positive bacteria, to induce NET extrusion from neutrophils firmly adhered to the glass slides coated with intercellular adhesion molecule-1(ICAM-1). We also used Sytox green to label NET-DNA and Flou-4 AM as the intracellular Ca 2+ signaling indicator to observe the NET formation and fluctuation of Ca 2+ signaling. Our results illustrated that LTA was able to induce NET release from neutrophils firmly attached to ICAM-1-coated glass slides, and the process was time-dependent. In addition, our study indicated that LTA-induced NET release by neutrophils stably adhered to ICAM-1 depended on Ca 2+ signaling but not intracellular reactive oxygen species (ROS). This study reveals NET formation mediated by direct interactions between endothelial ICAM-1 and neutrophils under LTA stimulation and key signaling molecules involved, providing the theoretical basis for medicine development and clinical treatment for related diseases.

[中性粒细胞细胞外捕获物在脂质亚基酸刺激下从稳定粘附在 ICAM-1 上的中性粒细胞中挤出]。
中性粒细胞胞外捕获物(NET)对促进血管内微血栓形成和加重脓毒症患者病情的影响已引起广泛关注。然而,在脓毒症中,内皮细胞和中性粒细胞直接相互作用时介导 NET 形成的机制和关键信号分子仍有待进一步探索。在此,我们利用革兰氏阳性细菌共有的一种成分--脂联素(LTA),诱导牢牢粘附在涂有细胞间粘附分子-1(ICAM-1)的玻璃载玻片上的中性粒细胞挤出NET。我们还使用 Sytox green 标记 NET-DNA 和 Flou-4 AM 作为细胞内 Ca 2+ 信号指示剂,以观察 NET 的形成和 Ca 2+ 信号的波动。我们的结果表明,LTA 能够诱导牢牢附着在涂有 ICAM-1 的玻璃载玻片上的中性粒细胞释放 NET,而且这一过程与时间有关。此外,我们的研究还表明,LTA 诱导稳定附着在 ICAM-1 上的中性粒细胞释放 NET 依赖于 Ca 2+ 信号,而不是细胞内活性氧(ROS)。本研究揭示了内皮 ICAM-1 与中性粒细胞在 LTA 刺激下直接相互作用介导的 NET 形成及其关键信号分子,为相关疾病的药物研发和临床治疗提供了理论依据。
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
生物医学工程学杂志
生物医学工程学杂志 Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
4868
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