• 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

来自MRL/lpr小鼠的成熟CD4+ T淋巴细胞对受体介导的耐受和凋亡具有抗性。

Mature CD4+ T lymphocytes from MRL/lpr mice are resistant to receptor-mediated tolerance and apoptosis.

作者信息

Bossu P, Singer G G, Andres P, Ettinger R, Marshak-Rothstein A, Abbas A K

机构信息

Department of Pathology, Brigham and Women's Hospital, Boston, MA.

出版信息

J Immunol. 1993 Dec 15;151(12):7233-9.

PMID:7903104
Abstract

The goal of this study was to examine the functional responses and tolerance susceptibility of T lymphocytes from mice of the autoimmune strain, MRL/lpr. A population of autoreactive CD4+ T cells can be readily expanded from the lymphoid tissues of young lpr mice. Lines of IL-2-producing autoreactive and alloreactive lpr and alloreactive +/+ T cells were developed to study their responses to tolerance-inducing stimuli. Culture of +/+ T cells with high concentrations of immobilized anti-CD3 antibody induces both functional anergy and apoptosis. By contrast, lpr-derived T cell lines are relatively resistant to anergy and apoptosis. The implications of these findings for the development of autoimmunity, and the possible role of the Fas Ag in determining resistance or susceptibility to tolerance, are discussed.

摘要

本研究的目的是检测自身免疫性品系MRL/lpr小鼠T淋巴细胞的功能反应和耐受敏感性。可轻易从小鼠幼崽的淋巴组织中扩增出一群自身反应性CD4+ T细胞。为了研究它们对诱导耐受刺激的反应,构建了产生白细胞介素-2的自身反应性、同种异体反应性lpr以及同种异体反应性+/+ T细胞系。用高浓度的固定化抗CD3抗体培养+/+ T细胞会诱导功能性无反应性和细胞凋亡。相比之下,源自lpr的T细胞系对无反应性和细胞凋亡具有相对抗性。讨论了这些发现对自身免疫性疾病发展的意义,以及Fas抗原在决定耐受抗性或敏感性方面可能发挥的作用。

相似文献

1
Mature CD4+ T lymphocytes from MRL/lpr mice are resistant to receptor-mediated tolerance and apoptosis.来自MRL/lpr小鼠的成熟CD4+ T淋巴细胞对受体介导的耐受和凋亡具有抗性。
J Immunol. 1993 Dec 15;151(12):7233-9.
2
Intact antigen receptor-mediated generation of inositol phosphates and increased intracellular calcium in CD4 CD8 T lymphocytes from MRL lpr mice.来自MRL lpr小鼠的CD4 CD8 T淋巴细胞中完整抗原受体介导的肌醇磷酸生成及细胞内钙增加。
J Immunol. 1990 Nov 1;145(9):2862-72.
3
Repeated 0.5-Gy gamma irradiation attenuates autoimmune disease in MRL-lpr/lpr mice with suppression of CD3+CD4-CD8-B220+ T-cell proliferation and with up-regulation of CD4+CD25+Foxp3+ regulatory T cells.重复进行0.5 Gy的γ射线照射可减轻MRL-lpr/lpr小鼠的自身免疫性疾病,其机制为抑制CD3+CD4-CD8-B220+ T细胞增殖并上调CD4+CD25+Foxp3+调节性T细胞。
Radiat Res. 2008 Jan;169(1):59-66. doi: 10.1667/RR1013.1.
4
Induction of allograft tolerance in the absence of Fas-mediated apoptosis.在缺乏Fas介导的细胞凋亡情况下诱导同种异体移植耐受。
J Immunol. 1999 Sep 1;163(5):2500-7.
5
Defective clonal deletion and anergy induction in TCR transgenic lpr/lpr mice.TCR转基因lpr/lpr小鼠中克隆清除和无反应性诱导缺陷。
Semin Immunol. 1994 Feb;6(1):27-37. doi: 10.1006/smim.1994.1005.
6
Restriction of the TCR repertoire inhibits the development of memory T cells and prevents autoimmunity in lpr mice.TCR库的限制会抑制记忆T细胞的发育,并预防lpr小鼠的自身免疫。
J Immunol. 1996 Jun 15;156(12):4961-8.
7
Recovery from autoimmunity of MRL/lpr mice after infection with an interleukin-2/vaccinia recombinant virus.感染白细胞介素-2/痘苗重组病毒后MRL/lpr小鼠自身免疫的恢复
Nature. 1990 Jul 19;346(6281):271-4. doi: 10.1038/346271a0.
8
Interleukin-2 reverses the defect in activation-induced apoptosis in T cells from autoimmune lpr mice.白细胞介素-2可逆转自身免疫性lpr小鼠T细胞中激活诱导的凋亡缺陷。
Cell Immunol. 1998 Jan 10;183(1):1-12. doi: 10.1006/cimm.1997.1233.
9
Dendritic cells are resistant to apoptosis through the Fas (CD95/APO-1) pathway.树突状细胞通过Fas(CD95/APO-1)途径对细胞凋亡具有抗性。
J Immunol. 1999 Nov 15;163(10):5303-11.
10
Memory T cell tolerance to superantigens is not due to increased susceptibility to apoptosis.记忆性T细胞对超抗原的耐受性并非源于对细胞凋亡敏感性的增加。
J Autoimmun. 1997 Aug;10(4):357-65. doi: 10.1006/jaut.1997.0146.

引用本文的文献

1
Cell cycle arrest caused by MEK/ERK signaling is a mechanism for suppressing growth of antigen-hyperstimulated effector T cells.由MEK/ERK信号传导引起的细胞周期停滞是抑制抗原过度刺激的效应T细胞生长的一种机制。
Int Immunol. 2016 Nov;28(11):547-557. doi: 10.1093/intimm/dxw037. Epub 2016 Aug 19.
2
Deletion of IL-18 Expression Ameliorates Spontaneous Kidney Failure in MRLlpr Mice.IL-18表达缺失改善MRLlpr小鼠的自发性肾衰竭。
PLoS One. 2015 Oct 14;10(10):e0140173. doi: 10.1371/journal.pone.0140173. eCollection 2015.
3
Bcl-2 knockdown accelerates T cell receptor-triggered activation-induced cell death in jurkat T cells.
Bcl-2 敲低加速 Jurkat T 细胞中 T 细胞受体触发的激活诱导细胞死亡。
Korean J Physiol Pharmacol. 2014 Feb;18(1):73-8. doi: 10.4196/kjpp.2014.18.1.73. Epub 2014 Feb 13.
4
Advances in lupus stemming from the parent-into-F1 model.狼疮研究的新进展源于亲代至 F1 代模型。
Trends Immunol. 2010 Jun;31(6):236-45. doi: 10.1016/j.it.2010.02.001. Epub 2010 Mar 31.
5
The influence of tobacco smoking on adhesion molecule profiles.吸烟对黏附分子谱的影响。
Tob Induc Dis. 2002 Jan 15;1(1):7-25. doi: 10.1186/1617-9625-1-1-7.
6
CD95 co-stimulation blocks activation of naive T cells by inhibiting T cell receptor signaling.CD95共刺激通过抑制T细胞受体信号传导来阻断初始T细胞的激活。
J Exp Med. 2009 Jun 8;206(6):1379-93. doi: 10.1084/jem.20082363. Epub 2009 Jun 1.
7
Fas expression on antigen-specific T cells has costimulatory, helper, and down-regulatory functions in vivo for cytotoxic T cell responses but not for T cell-dependent B cell responses.抗原特异性T细胞上的Fas表达在体内对细胞毒性T细胞反应具有共刺激、辅助和下调功能,但对T细胞依赖性B细胞反应则不然。
J Immunol. 2008 Nov 1;181(9):5912-29. doi: 10.4049/jimmunol.181.9.5912.
8
Mutation in the Fas pathway impairs CD8+ T cell memory.Fas信号通路中的突变会损害CD8 + T细胞记忆。
J Immunol. 2008 Mar 1;180(5):2933-41. doi: 10.4049/jimmunol.180.5.2933.
9
B cells in glomerulonephritis: focus on lupus nephritis.肾小球肾炎中的B细胞:聚焦狼疮性肾炎。
Semin Immunopathol. 2007 Nov;29(4):337-53. doi: 10.1007/s00281-007-0092-1. Epub 2007 Oct 18.
10
Targeting Notch signaling in autoimmune and lymphoproliferative disease.针对自身免疫性和淋巴细胞增生性疾病中的Notch信号通路
Blood. 2008 Jan 15;111(2):705-14. doi: 10.1182/blood-2007-05-087353. Epub 2007 Oct 9.