• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Afa/Dr diffusely adhering Escherichia coli strain C1845 induces neutrophil extracellular traps that kill bacteria and damage human enterocyte-like cells.Afa/Dr 弥漫粘附型大肠杆菌 C1845 株诱导中性粒细胞胞外诱捕网,可杀伤细菌并破坏人肠上皮样细胞。
Infect Immun. 2012 May;80(5):1891-9. doi: 10.1128/IAI.00050-12. Epub 2012 Feb 27.
2
Afa/Dr-expressing, diffusely adhering Escherichia coli strain C1845 triggers F1845 fimbria-dependent phosphatidylserine externalization on neutrophil-like differentiated PLB-985 cells through an apoptosis-independent mechanism.Afa/Dr 表达、弥漫黏附型大肠杆菌 C1845 菌株通过一种不依赖细胞凋亡的机制触发类似中性粒细胞分化的 PLB-985 细胞上 F1845 菌毛依赖性磷脂酰丝氨酸外化。
Infect Immun. 2010 Jul;78(7):2974-83. doi: 10.1128/IAI.01354-09. Epub 2010 Apr 19.
3
Afa/Dr diffusely adhering Escherichia coli infection in T84 cell monolayers induces increased neutrophil transepithelial migration, which in turn promotes cytokine-dependent upregulation of decay-accelerating factor (CD55), the receptor for Afa/Dr adhesins.T84细胞单层中Afa/Dr弥漫性黏附大肠杆菌感染会诱导中性粒细胞跨上皮迁移增加,这反过来又促进了衰变加速因子(CD55)的细胞因子依赖性上调,CD55是Afa/Dr黏附素的受体。
Infect Immun. 2003 Apr;71(4):1774-83. doi: 10.1128/IAI.71.4.1774-1783.2003.
4
Impairments in enzyme activity and biosynthesis of brush border-associated hydrolases in human intestinal Caco-2/TC7 cells infected by members of the Afa/Dr family of diffusely adhering Escherichia coli.被弥漫性黏附大肠杆菌Afa/Dr家族成员感染的人肠道Caco-2/TC7细胞中,刷状缘相关水解酶的酶活性和生物合成受损。
Cell Microbiol. 2001 May;3(5):341-57. doi: 10.1046/j.1462-5822.2001.00121.x.
5
Afa/Dr diffusely adhering Escherichia coli C1845 infection promotes selective injuries in the junctional domain of polarized human intestinal Caco-2/TC7 cells.Afa/Dr弥漫性黏附大肠杆菌C1845感染促进极化的人肠道Caco-2/TC7细胞连接区域的选择性损伤。
Infect Immun. 2000 Jun;68(6):3431-42. doi: 10.1128/IAI.68.6.3431-3442.2000.
6
Structural and functional lesions in brush border of human polarized intestinal Caco-2/TC7 cells infected by members of the Afa/Dr diffusely adhering family of Escherichia coli.被大肠杆菌Afa/Dr弥漫性黏附菌属成员感染的人极化肠Caco-2/TC7细胞刷状缘中的结构和功能损伤
Infect Immun. 2000 Oct;68(10):5979-90. doi: 10.1128/IAI.68.10.5979-5990.2000.
7
Recruitment of CD55 and CD66e brush border-associated glycosylphosphatidylinositol-anchored proteins by members of the Afa/Dr diffusely adhering family of Escherichia coli that infect the human polarized intestinal Caco-2/TC7 cells.Afa/Dr 家族的大肠杆菌成员招募 CD55 和 CD66e 刷状缘相关糖基磷脂酰肌醇锚定蛋白,这些大肠杆菌会感染人极化肠道 Caco-2/TC7 细胞。
Infect Immun. 2000 Jun;68(6):3554-63. doi: 10.1128/IAI.68.6.3554-3563.2000.
8
The secreted autotransporter toxin, Sat, functions as a virulence factor in Afa/Dr diffusely adhering Escherichia coli by promoting lesions in tight junction of polarized epithelial cells.分泌型自转运毒素Sat通过促进极化上皮细胞紧密连接的损伤,在Afa/Dr弥漫性黏附大肠杆菌中作为一种毒力因子发挥作用。
Cell Microbiol. 2007 Jan;9(1):204-21. doi: 10.1111/j.1462-5822.2006.00782.x. Epub 2006 Aug 11.
9
Piracy of decay-accelerating factor (CD55) signal transduction by the diffusely adhering strain Escherichia coli C1845 promotes cytoskeletal F-actin rearrangements in cultured human intestinal INT407 cells.弥漫性黏附菌株大肠杆菌C1845对衰变加速因子(CD55)信号转导的劫持促进了培养的人肠道INT407细胞中细胞骨架F-肌动蛋白的重排。
Infect Immun. 1998 Sep;66(9):4036-42. doi: 10.1128/IAI.66.9.4036-4042.1998.
10
Lactobacillus acidophilus (strain LB) from the resident adult human gastrointestinal microflora exerts activity against brush border damage promoted by a diarrhoeagenic Escherichia coli in human enterocyte-like cells.来自成年人体内常驻胃肠道微生物群的嗜酸乳杆菌(菌株LB)对人肠上皮样细胞中由致腹泻性大肠杆菌引发的刷状缘损伤具有抑制活性。
Gut. 2002 Jun;50(6):803-11. doi: 10.1136/gut.50.6.803.

引用本文的文献

1
Advances in acute COPD exacerbation: clarifying specific immune mechanisms of infectious and noninfectious factors.急性慢性阻塞性肺疾病加重的研究进展:阐明感染性和非感染性因素的特定免疫机制
Ther Adv Respir Dis. 2025 Jan-Dec;19:17534666241308408. doi: 10.1177/17534666241308408. Epub 2025 Mar 17.
2
The emerging role of neutrophil extracellular traps in autoimmune and autoinflammatory diseases.中性粒细胞胞外诱捕网在自身免疫性疾病和自身炎症性疾病中的新作用。
MedComm (2020). 2025 Mar 6;6(3):e70101. doi: 10.1002/mco2.70101. eCollection 2025 Mar.
3
Kuiyangling Enema Alleviates Ulcerative Colitis Mice by Reducing Levels of Intestinal NETs and Promoting HuR/VDR Signaling.溃炎灵灌肠剂通过降低肠道中性粒细胞胞外诱捕网水平和促进HuR/VDR信号传导来减轻溃疡性结肠炎小鼠症状。
J Inflamm Res. 2025 Jan 8;18:381-403. doi: 10.2147/JIR.S492818. eCollection 2025.
4
Neutrophil extracellular traps have active DNAzymes that promote bactericidal activity.中性粒细胞胞外诱捕网含有促进杀菌活性的活性脱氧核酶。
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkae1262.
5
-induced NETs are highly cytotoxic on hepatic and colonic cells due to serine proteases and myeloperoxidase activities.诱导产生的中性粒细胞胞外诱捕网由于丝氨酸蛋白酶和髓过氧化物酶的活性,对肝细胞和结肠细胞具有高度细胞毒性。
Front Immunol. 2024 Dec 2;15:1493946. doi: 10.3389/fimmu.2024.1493946. eCollection 2024.
6
Cytotoxic Oxidative Stress Effects of Neutrophil Extracellular Traps' Components on Cattle Spermatozoa.中性粒细胞胞外诱捕网成分对牛精子的细胞毒性氧化应激效应
Antioxidants (Basel). 2024 Jun 17;13(6):733. doi: 10.3390/antiox13060733.
7
Neutrophil Extracellular DNA Traps in Response to Infection or Inflammation, and the Roles of Platelet Interactions.中性粒细胞胞外DNA陷阱对感染或炎症的反应以及血小板相互作用的作用
Int J Mol Sci. 2024 Mar 5;25(5):3025. doi: 10.3390/ijms25053025.
8
Neutrophil extracellular traps in bacterial infections and evasion strategies.细菌感染中的中性粒细胞胞外诱捕网及逃逸策略
Front Immunol. 2024 Feb 16;15:1357967. doi: 10.3389/fimmu.2024.1357967. eCollection 2024.
9
Complement receptor 3 is required for maximum in vitro trogocytic killing of the parasite Trichomonas vaginalis by human neutrophil-like cells.补体受体 3 对于人中性粒细胞样细胞体外最大程度地吞噬寄生虫阴道毛滴虫是必需的。
Parasite Immunol. 2024 Feb;46(2):e13025. doi: 10.1111/pim.13025.
10
What is the role of the neutrophil extracellular traps in the cardiovascular disease burden associated with hemodialysis bioincompatibility?中性粒细胞胞外诱捕网在与血液透析生物不相容性相关的心血管疾病负担中起什么作用?
Front Med (Lausanne). 2023 Nov 15;10:1268748. doi: 10.3389/fmed.2023.1268748. eCollection 2023.

本文引用的文献

1
Systemic lupus erythematosus and the neutrophil.系统性红斑狼疮与中性粒细胞
N Engl J Med. 2011 Aug 25;365(8):758-60. doi: 10.1056/NEJMcibr1107085.
2
Eosinophil and neutrophil extracellular DNA traps in human allergic asthmatic airways.人过敏性哮喘气道中的嗜酸性粒细胞和中性粒细胞细胞外 DNA 陷阱。
J Allergy Clin Immunol. 2011 May;127(5):1260-6. doi: 10.1016/j.jaci.2010.12.1103. Epub 2011 Feb 18.
3
Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality.为一个事业而死:NETosis,一种抗菌细胞死亡方式的背后机制。
Cell Death Differ. 2011 Apr;18(4):581-8. doi: 10.1038/cdd.2011.1. Epub 2011 Feb 4.
4
Eosinophil extracellular DNA traps in skin diseases.皮肤病中外周血嗜酸性粒细胞胞外 DNA 陷阱
J Allergy Clin Immunol. 2011 Jan;127(1):194-9. doi: 10.1016/j.jaci.2010.11.002.
5
Neutrophil extracellular trap cell death requires both autophagy and superoxide generation.中性粒细胞胞外诱捕网细胞死亡需要自噬和超氧化物生成。
Cell Res. 2011 Feb;21(2):290-304. doi: 10.1038/cr.2010.150. Epub 2010 Nov 9.
6
Nuclease expression by Staphylococcus aureus facilitates escape from neutrophil extracellular traps.金黄色葡萄球菌的核酸酶表达促进了从中性粒细胞细胞外陷阱的逃逸。
J Innate Immun. 2010;2(6):576-86. doi: 10.1159/000319909. Epub 2010 Sep 10.
7
PAD4 is essential for antibacterial innate immunity mediated by neutrophil extracellular traps.PAD4 对于中性粒细胞胞外诱捕网介导的抗菌先天免疫是必需的。
J Exp Med. 2010 Aug 30;207(9):1853-62. doi: 10.1084/jem.20100239. Epub 2010 Aug 23.
8
Distinct cell death programs in monocytes regulate innate responses following challenge with common causes of invasive bacterial disease.不同的单核细胞死亡程序调节固有免疫反应,固有免疫反应是在受到常见侵袭性细菌疾病病原体的挑战后发生的。
J Immunol. 2010 Sep 1;185(5):2968-79. doi: 10.4049/jimmunol.1000805. Epub 2010 Jul 23.
9
Activated endothelial cells induce neutrophil extracellular traps and are susceptible to NETosis-mediated cell death.活化的内皮细胞诱导中性粒细胞胞外诱捕网的形成,并易发生 NETosis 介导的细胞死亡。
FEBS Lett. 2010 Jul 16;584(14):3193-7. doi: 10.1016/j.febslet.2010.06.006. Epub 2010 Jun 10.
10
Extracellular DNA: a major proinflammatory component of Pseudomonas aeruginosa biofilms.细胞外 DNA:铜绿假单胞菌生物膜的主要促炎成分。
J Immunol. 2010 Jun 1;184(11):6386-95. doi: 10.4049/jimmunol.0901640. Epub 2010 Apr 26.

Afa/Dr 弥漫粘附型大肠杆菌 C1845 株诱导中性粒细胞胞外诱捕网,可杀伤细菌并破坏人肠上皮样细胞。

Afa/Dr diffusely adhering Escherichia coli strain C1845 induces neutrophil extracellular traps that kill bacteria and damage human enterocyte-like cells.

机构信息

INSERM, UMR-S 996, Cytokines, Chemokines and Immunopathology, Châtenay-Malabry, France.

出版信息

Infect Immun. 2012 May;80(5):1891-9. doi: 10.1128/IAI.00050-12. Epub 2012 Feb 27.

DOI:10.1128/IAI.00050-12
PMID:22371374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3347451/
Abstract

We recently documented the neutrophil response to enterovirulent diffusely adherent Escherichia coli expressing Afa/Dr fimbriae (Afa/Dr DAEC), using the human myeloid cell line PLB-985 differentiated into fully mature neutrophils. Upon activation, particularly during infections, neutrophils release neutrophil extracellular traps (NETs), composed of a nuclear DNA backbone associated with antimicrobial peptides, histones, and proteases, which entrap and kill pathogens. Here, using fluorescence microscopy and field emission scanning electron microscopy, we observed NET production by PLB-985 cells infected with the Afa/Dr wild-type (WT) E. coli strain C1845. We found that these NETs were able to capture, immobilize, and kill WT C1845 bacteria. We also developed a coculture model of human enterocyte-like Caco-2/TC7 cells and PLB-985 cells previously treated with WT C1845 and found, for the first time, that the F-actin cytoskeleton of enterocyte-like cells is damaged in the presence of bacterium-induced NETs and that this deleterious effect is prevented by inhibition of protease release. These findings provide new insights into the neutrophil response to bacterial infection via the production of bactericidal NETs and suggest that NETs may damage the intestinal epithelium, particularly in situations such as inflammatory bowel diseases.

摘要

我们最近使用分化为完全成熟中性粒细胞的人髓样细胞系 PLB-985 记录了表达 Afa/Dr 菌毛的肠侵袭性弥漫性粘附性大肠杆菌(Afa/Dr DAEC)对中性粒细胞的反应。在激活过程中,特别是在感染期间,中性粒细胞会释放中性粒细胞细胞外陷阱(NETs),由与抗菌肽、组蛋白和蛋白酶相关的核 DNA 骨架组成,这些 NETs可以捕获和杀死病原体。在这里,我们使用荧光显微镜和场发射扫描电子显微镜观察了 Afa/Dr 野生型(WT)大肠杆菌菌株 C1845 感染 PLB-985 细胞产生的 NET。我们发现这些 NET 能够捕获、固定和杀死 WT C1845 细菌。我们还开发了一种人肠上皮样 Caco-2/TC7 细胞和 PLB-985 细胞的共培养模型,这些细胞先前用 WT C1845 处理过,我们首次发现,在细菌诱导的 NET 存在下,肠上皮样细胞的 F-肌动蛋白细胞骨架受损,而蛋白酶释放的抑制可防止这种有害影响。这些发现为中性粒细胞通过产生杀菌 NET 对细菌感染的反应提供了新的见解,并表明 NET 可能会损害肠道上皮,特别是在炎症性肠病等情况下。