T cells of different developmental stages differ in sensitivity to apoptosis induced by extracellular NAD.

Friedrich Haag, Dunja Freese, Felix Scheublein, Wiebke Ohlrogge, Sahil Adriouch, Michel Seman, Friedrich Koch-Nolte
{"title":"T cells of different developmental stages differ in sensitivity to apoptosis induced by extracellular NAD.","authors":"Friedrich Haag,&nbsp;Dunja Freese,&nbsp;Felix Scheublein,&nbsp;Wiebke Ohlrogge,&nbsp;Sahil Adriouch,&nbsp;Michel Seman,&nbsp;Friedrich Koch-Nolte","doi":"10.1080/10446670310001593514","DOIUrl":null,"url":null,"abstract":"<p><p>Extracellular nucleotides such as ATP and NAD can profoundly affect the functions of lymphocytes, macrophages, and other cells. We have recently shown that extracellular NAD induces rapid apoptosis in naive T cells by a mechanism involving the ADP-ribosylation of cell surface molecules. In the present paper, we describe that T cells of different developmental stages differ in their sensitivity to NAD-induced apoptosis. Thymocytes were less susceptible than peripheral lymph node T cells, and freshly activated cells were more resistant than resting cells. Sensitivity to NAD-induced apoptosis generally correlated with expression of the ADP-ribosyltransferase ART2.2, which is not expressed on thymocytes and shed from peripheral T cells upon activation. Our findings suggest that NAD-induced apoptosis does not play a role during thymic selection of T cells, but rather may play a role by preventing the activation of unwanted bystander T cells during an immune response, and thus may participate in the control of autoimmunity.</p>","PeriodicalId":77106,"journal":{"name":"Developmental immunology","volume":"9 4","pages":"197-202"},"PeriodicalIF":0.0000,"publicationDate":"2002-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/10446670310001593514","citationCount":"25","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10446670310001593514","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 25

Abstract

Extracellular nucleotides such as ATP and NAD can profoundly affect the functions of lymphocytes, macrophages, and other cells. We have recently shown that extracellular NAD induces rapid apoptosis in naive T cells by a mechanism involving the ADP-ribosylation of cell surface molecules. In the present paper, we describe that T cells of different developmental stages differ in their sensitivity to NAD-induced apoptosis. Thymocytes were less susceptible than peripheral lymph node T cells, and freshly activated cells were more resistant than resting cells. Sensitivity to NAD-induced apoptosis generally correlated with expression of the ADP-ribosyltransferase ART2.2, which is not expressed on thymocytes and shed from peripheral T cells upon activation. Our findings suggest that NAD-induced apoptosis does not play a role during thymic selection of T cells, but rather may play a role by preventing the activation of unwanted bystander T cells during an immune response, and thus may participate in the control of autoimmunity.

不同发育阶段的T细胞对细胞外NAD诱导的凋亡的敏感性不同。
细胞外核苷酸如ATP和NAD可以深刻影响淋巴细胞、巨噬细胞和其他细胞的功能。我们最近的研究表明,细胞外NAD通过一种涉及细胞表面分子adp核糖基化的机制诱导幼稚T细胞的快速凋亡。在本文中,我们描述了不同发育阶段的T细胞对nadd诱导的凋亡的敏感性不同。胸腺细胞比周围淋巴结T细胞更不敏感,新激活的细胞比静止的细胞更耐药。对nadd诱导的凋亡的敏感性通常与adp -核糖基转移酶ART2.2的表达相关,该酶在胸腺细胞上不表达,激活后会从外周T细胞脱落。我们的研究结果表明,nad诱导的细胞凋亡并不在T细胞的胸腺选择中起作用,而是在免疫反应中通过阻止不需要的旁观者T细胞的激活发挥作用,从而可能参与自身免疫的控制。
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