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多种受体-配体相互作用直接介导组织驻留γδ T细胞活化。

Multiple Receptor-Ligand Interactions Direct Tissue-Resident γδ T Cell Activation.

作者信息

Witherden Deborah A, Ramirez Kevin, Havran Wendy L

机构信息

Department of Immunology and Microbial Science, The Scripps Research Institute , La Jolla, CA , USA.

出版信息

Front Immunol. 2014 Nov 24;5:602. doi: 10.3389/fimmu.2014.00602. eCollection 2014.

Abstract

γδ T cells represent a major T cell population in epithelial tissues, such as skin, intestine, and lung, where they function in maintenance of the epithelium and provide a crucial first line defense against environmental and pathogenic insults. Despite their importance, the molecular mechanisms directing their activation and function have remained elusive. Epithelial-resident γδ T cells function through constant communication with neighboring cells, either via direct cell-to-cell contact or cell-to-matrix interactions. These intimate relationships allow γδ T cells to facilitate the maintenance of epithelial homeostasis, tissue repair following injury, inflammation, and protection from malignancy. Recent studies have identified a number of molecules involved in these complex interactions, under both homeostatic conditions, as well as following perturbation of these barrier tissues. These interactions are crucial to the timely production of cytokines, chemokines, growth factors, and extracellular matrix proteins for restoration of homeostasis. In this review, we discuss recent advances in understanding the mechanisms directing epithelial-T cell crosstalk and the distinct roles played by individual receptor-ligand pairs of cell surface molecules in this process.

摘要

γδ T细胞是上皮组织(如皮肤、肠道和肺)中的主要T细胞群体,它们在维持上皮组织功能方面发挥作用,并提供抵御环境和病原体侵害的关键第一道防线。尽管它们很重要,但其激活和功能的分子机制仍然难以捉摸。上皮组织驻留的γδ T细胞通过与相邻细胞持续通讯发挥作用,通讯方式包括直接的细胞间接触或细胞与基质的相互作用。这些密切关系使γδ T细胞能够促进上皮内环境稳定的维持、损伤后的组织修复、炎症反应以及预防恶性肿瘤。最近的研究已经确定了许多参与这些复杂相互作用的分子情况,这些情况既存在于稳态条件下,也存在于这些屏障组织受到干扰之后。这些相互作用对于及时产生细胞因子、趋化因子、生长因子和细胞外基质蛋白以恢复内环境稳定至关重要。在这篇综述中,我们讨论了在理解上皮细胞与T细胞相互作用机制方面的最新进展,以及在此过程中细胞表面分子的各个受体-配体对所发挥的不同作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e385/4241470/eb20cfb25856/fimmu-05-00602-g001.jpg

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