Yersinia Pseudotuberculosis Modulates Regulatory T Cell Stability via Injection of Yersinia Outer Proteins in a Type III Secretion System-Dependent Manner.

European Journal of Microbiology & Immunology Pub Date : 2018-11-28 eCollection Date: 2018-12-23 DOI:10.1556/1886.2018.00015
Ahmed Elfiky, Agnes Bonifacius, Joern Pezoldt, Maria Pasztoi, Paweena Chaoprasid, Pooja Sadana, Nagla El-Sherbeeny, Magda Hagras, Andrea Scrima, Petra Dersch, Jochen Huehn
{"title":"<i>Yersinia Pseudotuberculosis</i> Modulates Regulatory T Cell Stability via Injection of Yersinia Outer Proteins in a Type III Secretion System-Dependent Manner.","authors":"Ahmed Elfiky,&nbsp;Agnes Bonifacius,&nbsp;Joern Pezoldt,&nbsp;Maria Pasztoi,&nbsp;Paweena Chaoprasid,&nbsp;Pooja Sadana,&nbsp;Nagla El-Sherbeeny,&nbsp;Magda Hagras,&nbsp;Andrea Scrima,&nbsp;Petra Dersch,&nbsp;Jochen Huehn","doi":"10.1556/1886.2018.00015","DOIUrl":null,"url":null,"abstract":"<p><p>Adaptive immunity is essentially required to control acute infection with enteropathogenic <i>Yersinia pseudotuberculosis</i> (Yptb). We have recently demonstrated that Yptb can directly modulate naïve CD4<sup>+</sup> T cell differentiation. However, whether fully differentiated forkhead box protein P3 (Foxp3<sup>+</sup>) regulatory T cells (Tregs), fundamental key players to maintain immune homeostasis, are targeted by Yptb remains elusive. Here, we demonstrate that within the CD4<sup>+</sup> T cell compartment Yptb preferentially targets Tregs and injects Yersinia outer proteins (Yops) in a process that depends on the type III secretion system and invasins. Remarkably, Yop-translocation into ex vivo isolated Foxp3<sup>+</sup> Tregs resulted in a substantial downregulation of Foxp3 expression and a decreased capacity to express the immunosuppressive cytokine interleukin-10 (IL-10). Together, these findings highlight that invasins are critically required to mediate Yptb attachment to Foxp3<sup>+</sup> Tregs, which allows efficient Yop-translocation and finally enables the modulation of the Foxp3<sup>+</sup> Tregs' suppressive phenotype.</p>","PeriodicalId":11929,"journal":{"name":"European Journal of Microbiology & Immunology","volume":"8 4","pages":"101-106"},"PeriodicalIF":0.0000,"publicationDate":"2018-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1556/1886.2018.00015","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Microbiology & Immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1556/1886.2018.00015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/12/23 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

Adaptive immunity is essentially required to control acute infection with enteropathogenic Yersinia pseudotuberculosis (Yptb). We have recently demonstrated that Yptb can directly modulate naïve CD4+ T cell differentiation. However, whether fully differentiated forkhead box protein P3 (Foxp3+) regulatory T cells (Tregs), fundamental key players to maintain immune homeostasis, are targeted by Yptb remains elusive. Here, we demonstrate that within the CD4+ T cell compartment Yptb preferentially targets Tregs and injects Yersinia outer proteins (Yops) in a process that depends on the type III secretion system and invasins. Remarkably, Yop-translocation into ex vivo isolated Foxp3+ Tregs resulted in a substantial downregulation of Foxp3 expression and a decreased capacity to express the immunosuppressive cytokine interleukin-10 (IL-10). Together, these findings highlight that invasins are critically required to mediate Yptb attachment to Foxp3+ Tregs, which allows efficient Yop-translocation and finally enables the modulation of the Foxp3+ Tregs' suppressive phenotype.

Abstract Image

Abstract Image

Abstract Image

假结核耶尔森菌通过注射耶尔森菌外蛋白以III型分泌系统依赖的方式调节调节性T细胞的稳定性。
适应性免疫是控制肠致病性假结核耶尔森菌(Yptb)急性感染的必要条件。我们最近证明了Yptb可以直接调节naïve CD4+ T细胞分化。然而,完全分化的叉头盒蛋白P3 (Foxp3+)调节性T细胞(Tregs)作为维持免疫稳态的关键角色,是否被Yptb靶向仍然是未知的。在这里,我们证明了在CD4+ T细胞室内,Yptb优先靶向Tregs并在依赖于III型分泌系统和入侵的过程中注射耶尔森氏菌外蛋白(Yops)。值得注意的是,yop易位到离体分离的Foxp3+ Tregs中导致Foxp3表达显著下调,免疫抑制细胞因子白介素-10 (IL-10)表达能力下降。总之,这些发现强调了入侵蛋白是介导Yptb附着在Foxp3+ Tregs上的关键,这允许有效的yop易位,并最终实现Foxp3+ Tregs抑制表型的调节。
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
自引率
0.00%
发文量
0
×
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