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稳态下淋巴结内T细胞迁移动力学:影响基础淋巴结内T细胞运动性的细胞外和细胞内因素概述

T cell migration dynamics within lymph nodes during steady state: an overview of extracellular and intracellular factors influencing the basal intranodal T cell motility.

作者信息

Worbs Tim, Förster Reinhold

机构信息

Institute of Immunology, Hannover Medical School, Carl-Neuberg-Strasse 1, Hannover, Germany.

出版信息

Curr Top Microbiol Immunol. 2009;334:71-105. doi: 10.1007/978-3-540-93864-4_4.

DOI:10.1007/978-3-540-93864-4_4
PMID:19521682
Abstract

Naive T lymphocytes continuously recirculate through secondary lymphoid organs such as lymph nodes until they are eventually activated by recognizing cognate peptide/MHC-complexes on the surface of antigen-protecting cells. The intranodal T cell migration behavior leading to these crucial--and potentially rare--encounters during the induction of an adaptive immune response could not be directly addressed until, in 2002, the use of two-photon microscopy also allowed the visualization of cellular dynamics deep within intact lymph nodes. Since then, numerous studies have confirmed that, by default, naive T cells are extremely motile, scanning the paracortical T cell zone for cognate antigen by means of an apparent random walk. This review attempts to summarize the current knowledge of factors influencing the basal migration behavior of naive T lymphocytes within lymph nodes during steady state. Extracellular cues, such as the motility-promoting influence of CCR7 ligands and the role of integrins during interstitial migration, as well as intracellular signaling pathways involved in T cell motility, will be discussed. Particular emphasis is placed on structural features of the lymph node environment orchestrating T cell migration, namely the framework of fibroblastic reticular cells serving as migration "highways." Finally, new approaches to simulate the cellular dynamics within lymph nodes in silico by means of mathematical modeling will be reviewed.

摘要

初始T淋巴细胞持续不断地在诸如淋巴结等二级淋巴器官中循环,直到它们最终通过识别抗原呈递细胞表面的同源肽/MHC复合物而被激活。在2002年之前,由于无法直接观察到适应性免疫应答诱导过程中导致这些关键(且可能罕见)相遇的结内T细胞迁移行为,直到双光子显微镜的应用使得在完整淋巴结内部深处的细胞动态可视化。从那时起,大量研究证实,在默认情况下,初始T细胞具有极高的运动性,通过明显的随机游走在副皮质T细胞区扫描同源抗原。本综述试图总结目前关于稳态期间影响淋巴结内初始T淋巴细胞基础迁移行为的因素的知识。将讨论细胞外信号,如CCR7配体的促运动影响以及整合素在间质迁移中的作用,以及参与T细胞运动的细胞内信号通路。特别强调协调T细胞迁移的淋巴结环境的结构特征,即作为迁移“高速公路”的成纤维网状细胞框架。最后,将综述通过数学建模在计算机上模拟淋巴结内细胞动态的新方法。

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New tools for immunologists: models of lymph node function from cells to tissues.免疫学家的新工具:从细胞到组织的淋巴结功能模型。
Front Immunol. 2023 May 10;14:1183286. doi: 10.3389/fimmu.2023.1183286. eCollection 2023.
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Spatial Lymphocyte Dynamics in Lymph Nodes Predicts the Cytotoxic T Cell Frequency Needed for HIV Infection Control.
淋巴结中淋巴细胞的空间动力学可预测控制 HIV 感染所需的细胞毒性 T 细胞频率。
Front Immunol. 2019 Jun 11;10:1213. doi: 10.3389/fimmu.2019.01213. eCollection 2019.
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The actin-bundling protein L-plastin supports T-cell motility and activation.肌动蛋白结合蛋白 L-肌动蛋白支持 T 细胞的迁移和激活。
Immunol Rev. 2013 Nov;256(1):48-62. doi: 10.1111/imr.12102.
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Impaired T-cell responses to sphingosine-1-phosphate in HIV-1 infected lymph nodes.HIV-1 感染淋巴结中鞘氨醇-1-磷酸诱导的 T 细胞反应受损。
Blood. 2013 Apr 11;121(15):2914-22. doi: 10.1182/blood-2012-07-445783. Epub 2013 Feb 19.
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On-lattice simulation of T cell motility, chemotaxis, and trafficking in the lymph node paracortex.在淋巴结皮层中 T 细胞迁移、趋化和运输的晶格模拟。
PLoS One. 2012;7(9):e45258. doi: 10.1371/journal.pone.0045258. Epub 2012 Sep 19.
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Influence of the fibroblastic reticular network on cell-cell interactions in lymphoid organs.成纤维网状细胞网络对淋巴器官中细胞间相互作用的影响。
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Homeostatic signals do not drive post-thymic T cell maturation.稳态信号不会驱动胸腺后 T 细胞成熟。
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