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本文引用的文献

1
Intrinsic properties of immunoglobulin IgG1 isotype-switched B cell receptors promote microclustering and the initiation of signaling.免疫球蛋白IgG1同种型转换B细胞受体的内在特性促进微簇集和信号传导的启动。
Immunity. 2010 Jun 25;32(6):778-89. doi: 10.1016/j.immuni.2010.06.006.
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Dynamics of subsynaptic vesicles and surface microclusters at the immunological synapse.免疫突触中突触小泡和表面微簇的动力学。
Sci Signal. 2010 May 11;3(121):ra36. doi: 10.1126/scisignal.2000645.
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The kinetics of two-dimensional TCR and pMHC interactions determine T-cell responsiveness.二维 TCR 和 pMHC 相互作用的动力学决定了 T 细胞的反应性。
Nature. 2010 Apr 8;464(7290):932-6. doi: 10.1038/nature08944. Epub 2010 Mar 31.
4
TCR-peptide-MHC interactions in situ show accelerated kinetics and increased affinity.TCR-肽-MHC 相互作用的原位显示出加速的动力学和增加的亲和力。
Nature. 2010 Feb 18;463(7283):963-7. doi: 10.1038/nature08746.
5
Hematopoietic lineage cell-specific protein 1 is recruited to the immunological synapse by IL-2-inducible T cell kinase and regulates phospholipase Cgamma1 Microcluster dynamics during T cell spreading.造血谱系细胞特异性蛋白1被白细胞介素-2诱导型T细胞激酶募集到免疫突触,并在T细胞铺展过程中调节磷脂酶Cγ1微簇动力学。
J Immunol. 2009 Dec 1;183(11):7352-61. doi: 10.4049/jimmunol.0900973. Epub 2009 Nov 16.
6
Kinetics of early T cell receptor signaling regulate the pathway of lytic granule delivery to the secretory domain.早期T细胞受体信号传导的动力学调控着溶细胞颗粒向分泌结构域递送的途径。
Immunity. 2009 Oct 16;31(4):632-42. doi: 10.1016/j.immuni.2009.09.004.
7
The strength of T cell receptor signal controls the polarization of cytotoxic machinery to the immunological synapse.T细胞受体信号的强度控制着细胞毒性机制向免疫突触的极化。
Immunity. 2009 Oct 16;31(4):621-31. doi: 10.1016/j.immuni.2009.08.024.
8
Microsignalosomes: spatially resolved receptor signalling.微信号体:空间分辨的受体信号传导
Biochem Soc Trans. 2009 Oct;37(Pt 5):1014-8. doi: 10.1042/BST0371014.
9
Investigating CTL mediated killing with a 3D cellular automaton.用三维细胞自动机研究细胞毒性T淋巴细胞介导的杀伤作用。
PLoS Comput Biol. 2009 Aug;5(8):e1000466. doi: 10.1371/journal.pcbi.1000466. Epub 2009 Aug 21.
10
Localized diacylglycerol drives the polarization of the microtubule-organizing center in T cells.局部二酰基甘油驱动T细胞中微管组织中心的极化。
Nat Immunol. 2009 Jun;10(6):627-35. doi: 10.1038/ni.1734.

T 细胞受体信号转导动力学成为焦点。

T cell receptor signaling kinetics takes the stage.

机构信息

Department of Microbiology and Immunology and Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Sci Signal. 2010 Dec 21;3(153):pe50. doi: 10.1126/scisignal.3153pe50.

DOI:10.1126/scisignal.3153pe50
PMID:21177491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3040109/
Abstract

It has been long surmised that the strength of stimulation of the T cell receptor (TCR) determines the robustness of TCR-mediated signaling and the magnitude of a T cell response. However, it is becoming evident that the signal from the TCR develops over time to approach its steady-state, affinity-determined maximal extent and that variations in this time have a substantial effect on the responsiveness of T cells. Here, I discuss data that show that the kinetics of signal propagation in various segments of the TCR signaling network can influence the spatiotemporal regulation of the effector functions of T cells and the quality of the T cell response.

摘要

长期以来,人们一直推测 T 细胞受体 (TCR) 的刺激强度决定了 TCR 介导的信号转导的稳健性以及 T 细胞反应的幅度。然而,现在越来越明显的是,TCR 的信号随着时间的推移而发展,趋近于其稳态、亲和力决定的最大程度,而这种时间上的变化对 T 细胞的反应性有很大的影响。在这里,我讨论了一些数据,这些数据表明 TCR 信号转导网络的各个部分中信号传播的动力学可以影响 T 细胞效应功能的时空调节以及 T 细胞反应的质量。