• 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
The conundrum of inhibitory signaling by ITAM-containing immunoreceptors: potential molecular mechanisms.含 ITAM 的免疫受体抑制信号转导的难题:潜在的分子机制。
FEBS Lett. 2010 Dec 15;584(24):4878-82. doi: 10.1016/j.febslet.2010.09.029. Epub 2010 Sep 28.
2
Asymmetrical phosphorylation and function of immunoreceptor tyrosine-based activation motif tyrosines in B cell antigen receptor signal transduction.基于免疫受体酪氨酸的激活基序酪氨酸在B细胞抗原受体信号转导中的不对称磷酸化及功能
J Immunol. 1998 Apr 1;160(7):3305-14.
3
Inhibitory ITAMs as novel regulators of immunity.抑制性 ITAMs 作为免疫调节的新靶点。
Immunol Rev. 2009 Nov;232(1):59-71. doi: 10.1111/j.1600-065X.2009.00832.x.
4
Inhibition of immune responses by ITAM-bearing receptors.含免疫受体酪氨酸激活基序(ITAM)的受体对免疫反应的抑制作用。
Sci STKE. 2006 Jan 31;2006(320):re1. doi: 10.1126/stke.3202006re1.
5
Immunoreceptor tyrosine-based inhibitory motif (ITIM)-mediated inhibitory signaling is regulated by sequential phosphorylation mediated by distinct nonreceptor tyrosine kinases: a case study involving PECAM-1.免疫受体酪氨酸抑制基序 (ITIM) 介导的抑制信号受不同非受体酪氨酸激酶介导的顺序磷酸化调节:以 PECAM-1 为例。
Biochemistry. 2013 Apr 16;52(15):2597-608. doi: 10.1021/bi301461t. Epub 2013 Apr 3.
6
Phosphorylated immunoreceptor signaling motifs (ITAMs) exhibit unique abilities to bind and activate Lyn and Syk tyrosine kinases.磷酸化免疫受体信号基序(ITAMs)具有结合并激活Lyn和Syk酪氨酸激酶的独特能力。
J Immunol. 1995 Nov 15;155(10):4596-603.
7
Immunoreceptor tyrosine-based activation motif (ITAM), a unique module linking antigen and Fc receptors to their signaling cascades.基于免疫受体酪氨酸的激活基序(ITAM),是一种将抗原和Fc受体与其信号级联相连接的独特模块。
J Leukoc Biol. 1997 Jan;61(1):6-16. doi: 10.1002/jlb.61.1.6.
8
Bovine leukemia virus gp30 transmembrane (TM) protein is not tyrosine phosphorylated: examining potential interactions with host tyrosine-mediated signaling.牛白血病病毒糖蛋白30跨膜(TM)蛋白未发生酪氨酸磷酸化:探究其与宿主酪氨酸介导信号传导的潜在相互作用。
Virus Res. 2002 Dec;90(1-2):155-69. doi: 10.1016/s0168-1702(02)00149-1.
9
The B cell receptor promotes B cell activation and proliferation through a non-ITAM tyrosine in the Igalpha cytoplasmic domain.B细胞受体通过Igalpha胞质结构域中的一个非免疫受体酪氨酸激活基序酪氨酸促进B细胞活化和增殖。
Immunity. 2006 Jul;25(1):55-65. doi: 10.1016/j.immuni.2006.04.014.
10
Inhibitory ITAMs: a matter of life and death.抑制性免疫受体酪氨酸激活基序:生死攸关之事。
Trends Immunol. 2008 Aug;29(8):366-73. doi: 10.1016/j.it.2008.05.001. Epub 2008 Jul 2.

引用本文的文献

1
Early events in TCR signaling - the evolving role of ITAMs.TCR信号传导的早期事件——免疫受体酪氨酸活化基序不断演变的作用
Front Immunol. 2025 Apr 24;16:1563049. doi: 10.3389/fimmu.2025.1563049. eCollection 2025.
2
Immunoregulatory Property of C-Type Lectin-Like Receptors in Fibrosing Interstitial Lung Diseases.C 型凝集素样受体在纤维性间质性肺疾病中的免疫调节特性。
Int J Mol Sci. 2020 May 22;21(10):3665. doi: 10.3390/ijms21103665.
3
The MS4A family: counting past 1, 2 and 3.MS4A家族:超过1、2和3的计数
Immunol Cell Biol. 2016 Jan;94(1):11-23. doi: 10.1038/icb.2015.48. Epub 2015 Apr 3.
4
The outcome of B-cell receptor signaling in chronic lymphocytic leukemia: proliferation or anergy.慢性淋巴细胞白血病中B细胞受体信号传导的结果:增殖或无反应性。
Haematologica. 2014 Jul;99(7):1138-48. doi: 10.3324/haematol.2013.098384.
5
Multigene families of immunoglobulin domain-containing innate immune receptors in zebrafish: deciphering the differences.斑马鱼中含免疫球蛋白结构域的天然免疫受体多基因家族:解读差异
Dev Comp Immunol. 2014 Sep;46(1):24-34. doi: 10.1016/j.dci.2014.02.004. Epub 2014 Feb 15.
6
Deletion of microRNA-155 reduces autoantibody responses and alleviates lupus-like disease in the Fas(lpr) mouse.缺失 microRNA-155 可减少自身抗体反应并缓解 Fas(lpr)小鼠的狼疮样疾病。
Proc Natl Acad Sci U S A. 2013 Dec 10;110(50):20194-9. doi: 10.1073/pnas.1317632110. Epub 2013 Nov 26.
7
Phosphatase regulation of immunoreceptor signaling in T cells, B cells and mast cells.磷酸酶对 T 细胞、B 细胞和肥大细胞中免疫受体信号的调节作用。
Curr Opin Immunol. 2013 Jun;25(3):313-20. doi: 10.1016/j.coi.2013.04.001. Epub 2013 May 15.
8
Human lupus serum induces neutrophil-mediated organ damage in mice that is enabled by Mac-1 deficiency.人狼疮血清诱导 Mac-1 缺陷小鼠中性粒细胞介导的器官损伤。
J Immunol. 2012 Oct 1;189(7):3714-23. doi: 10.4049/jimmunol.1201594. Epub 2012 Aug 29.
9
The adaptor protein SAP directly associates with CD3ζ chain and regulates T cell receptor signaling.衔接蛋白 SAP 直接与 CD3ζ 链结合,并调节 T 细胞受体信号转导。
PLoS One. 2012;7(8):e43200. doi: 10.1371/journal.pone.0043200. Epub 2012 Aug 13.
10
Bench-to-bedside review: Immunoglobulin therapy for sepsis - biological plausibility from a critical care perspective.从实验室到临床的综述:脓毒症的免疫球蛋白治疗——从重症监护角度看其生物学合理性
Crit Care. 2012 Dec 12;16(2):206. doi: 10.1186/cc10597.

本文引用的文献

1
Inhibitory ITAMs as novel regulators of immunity.抑制性 ITAMs 作为免疫调节的新靶点。
Immunol Rev. 2009 Nov;232(1):59-71. doi: 10.1111/j.1600-065X.2009.00832.x.
2
Suppression of phosphatidylinositol 3,4,5-trisphosphate production is a key determinant of B cell anergy.磷脂酰肌醇3,4,5-三磷酸生成的抑制是B细胞无能的关键决定因素。
Immunity. 2009 Nov 20;31(5):749-60. doi: 10.1016/j.immuni.2009.08.026. Epub 2009 Nov 5.
3
Immunoreceptor tyrosine-based inhibition motifs: a quest in the past and future.基于免疫受体酪氨酸的抑制基序:过去与未来的探索
Immunol Rev. 2008 Aug;224:11-43. doi: 10.1111/j.1600-065X.2008.00666.x.
4
Inhibitory ITAM signaling by Fc alpha RI-FcR gamma chain controls multiple activating responses and prevents renal inflammation.通过FcαRI-FcRγ链进行的抑制性免疫受体酪氨酸激活基序信号传导可控制多种激活反应并预防肾脏炎症。
J Immunol. 2008 Feb 15;180(4):2669-78. doi: 10.4049/jimmunol.180.4.2669.
5
Regulation of B-cell development by BCAP and CD19 through their binding to phosphoinositide 3-kinase.BCAP和CD19通过与磷酸肌醇3激酶结合对B细胞发育进行调控。
Blood. 2008 Feb 1;111(3):1497-503. doi: 10.1182/blood-2007-08-109769. Epub 2007 Nov 19.
6
Calcium signalling and cell-fate choice in B cells.B细胞中的钙信号传导与细胞命运抉择
Nat Rev Immunol. 2007 Oct;7(10):778-89. doi: 10.1038/nri2172.
7
B cell-specific deletion of protein-tyrosine phosphatase Shp1 promotes B-1a cell development and causes systemic autoimmunity.蛋白酪氨酸磷酸酶Shp1在B细胞中的特异性缺失促进B-1a细胞发育并导致系统性自身免疫。
Immunity. 2007 Jul;27(1):35-48. doi: 10.1016/j.immuni.2007.04.016. Epub 2007 Jun 28.
8
Defining SH2 domain and PTP specificity by screening combinatorial peptide libraries.通过筛选组合肽库定义SH2结构域和蛋白酪氨酸磷酸酶特异性
Methods. 2007 Jul;42(3):207-19. doi: 10.1016/j.ymeth.2007.02.010.
9
Fc alpha receptor I activation induces leukocyte recruitment and promotes aggravation of glomerulonephritis through the FcR gamma adaptor.Fcα受体I激活通过FcRγ衔接蛋白诱导白细胞募集并促进肾小球肾炎的加重。
Eur J Immunol. 2007 Apr;37(4):1116-28. doi: 10.1002/eji.200636826.
10
Cutting Edge: Acute and chronic exposure of immature B cells to antigen leads to impaired homing and SHIP1-dependent reduction in stromal cell-derived factor-1 responsiveness.前沿:未成熟B细胞急性和慢性暴露于抗原会导致归巢受损以及依赖SHIP1的基质细胞衍生因子-1反应性降低。
J Immunol. 2007 Mar 15;178(6):3353-7. doi: 10.4049/jimmunol.178.6.3353.

含 ITAM 的免疫受体抑制信号转导的难题:潜在的分子机制。

The conundrum of inhibitory signaling by ITAM-containing immunoreceptors: potential molecular mechanisms.

机构信息

Integrated Department of Immunology, University of Colorado School of Medicine, Denver CO 80206, USA.

出版信息

FEBS Lett. 2010 Dec 15;584(24):4878-82. doi: 10.1016/j.febslet.2010.09.029. Epub 2010 Sep 28.

DOI:10.1016/j.febslet.2010.09.029
PMID:20875413
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2998577/
Abstract

Immunoreceptor signals must be appropriately transduced and regulated to achieve effective immunity while controlling inflammation and autoimmunity. It is generally held that these processes are mediated by the interplay of distinct activating and inhibitory receptors via conserved activating (ITAM) and inhibitory (ITIM) signaling motifs. However, recent evidence indicates that under certain conditions incomplete phosphorylation of ITAM tyrosines leads to inhibitory signaling. This new regulatory function of ITAMs has been termed ITAMi (inhibitory ITAM). Here we discuss the potential molecular mechanisms of inhibitory signaling by ITAM-containing receptors.

摘要

免疫受体信号必须进行适当的转导和调节,以在控制炎症和自身免疫的同时实现有效的免疫。人们普遍认为,这些过程是通过独特的激活和抑制受体通过保守的激活(ITAM)和抑制(ITIM)信号基序的相互作用来介导的。然而,最近的证据表明,在某些条件下,ITAM 酪氨酸的不完全磷酸化会导致抑制性信号。这种 ITAM 的新调节功能被称为 ITAMi(抑制性 ITAM)。在这里,我们讨论了含 ITAM 受体的抑制性信号传递的潜在分子机制。