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Visualizing T Cell Migration in situ

机译:可视化原位T细胞迁移

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摘要

Mounting a protective immune response is critically dependent on the orchestrated movement of cells within lymphoid tissues. The structure of secondary lymphoid organs regulates immune responses by promoting optimal cell–cell and cell–extracellular matrix interactions. Naïve T cells are initially activated by antigen presenting cells in secondary lymphoid organs. Following priming, effector T cells migrate to the site of infection to exert their functions. Majority of the effector cells die while a small population of antigen-specific T cells persists as memory cells in distinct anatomical locations. The persistence and location of memory cells in lymphoid and non-lymphoid tissues is critical to protect the host from re-infection. The localization of memory T cells is carefully regulated by several factors including the highly organized secondary lymphoid structure, the cellular expression of chemokine receptors and compartmentalized secretion of their cognate ligands. This balance between the anatomy and the ordered expression of cell surface and soluble proteins regulates the subtle choreography of T cell migration. In recent years, our understanding of cellular dynamics of T cells has been advanced by the development of new imaging techniques allowing in situ visualization of T cell responses. Here, we review the past and more recent studies that have utilized sophisticated imaging technologies to investigate the migration dynamics of naïve, effector, and memory T cells.
机译:进行保护性免疫应答至关重要地取决于淋巴组织内细胞的协调运动。次生淋巴器官的结构通过促进最佳的细胞间和细胞外细胞间的相互作用来调节免疫反应。幼稚的T细胞最初被次级淋巴器官中的抗原呈递细胞激活。启动后,效应T细胞迁移到感染部位以发挥其功能。大多数效应细胞死亡,而一小部分抗原特异性T细胞作为记忆细胞在不同的解剖部位持续存在。淋巴和非淋巴组织中记忆细胞的持久性和位置对于保护宿主免于再次感染至关重要。记忆T细胞的定位受几个因素的精心调节,包括高度组织化的二级淋巴样结构,趋化因子受体的细胞表达以及其同源配体的区室分泌。解剖结构与细胞表面和可溶性蛋白质的有序表达之间的这种平衡调节了T细胞迁移的精细编排。近年来,通过新成像技术的发展,我们对T细胞的细胞动力学有了更深入的了解,从而可以对T细胞反应进行原位观察。在这里,我们回顾了过去和最近的研究,这些研究已经利用先进的成像技术来研究幼稚,效应和记忆T细胞的迁移动力学。

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