CD4+ T 辅助细胞对肥大细胞的替代性激活。

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Edouard Leveque, Louise Battut, Camille Petitfils, Salvatore Valitutti, Nicolas Cenac, Gilles Dietrich, Eric Espinosa
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引用次数: 0

摘要

效应 CD4+ T 淋巴细胞(Teff)渗入炎症部位,通过指示当地白细胞来协调免疫反应。肥大细胞(MC)是组织哨兵细胞,战略性地分布在血管和 T 细胞丰富的区域附近。MC/Teff细胞之间的相互作用影响着Teff细胞的反应,但反过来,Teff细胞对MC的作用仍鲜为人知。在这里,我们通过应用 RNAseq 和功能测试分析了人类 MC/Teff 细胞的相互作用。我们发现,活化的 Teff 细胞会诱导 MCs 产生特定的转录组程序,包括产生炎症细胞因子和趋化因子、前列腺素,以及依赖于 FcεRI 的脱颗粒促进作用,从而促使 MCs 形成炎症表型。此外,Teff 细胞还能通过多种专用的可溶性和膜配体诱导 MCs 与 CD4+ T 细胞相互作用,并发挥抗原呈递细胞(APCs)的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alternative activation of mast cells by CD4+ T helper cells.

Effector CD4+ T (Teff) lymphocytes infiltrate sites of inflammation and orchestrate the immune response by instructing local leukocytes. Mast cells (MCs) are tissue sentinel cells strategically located near blood vessels and T cell-rich areas. MC/Teff cell interactions shape Teff cell responses, but in turn, Teff cell action on MCs is still poorly understood. Here, we analyzed the human MC/Teff cell interplay through both the application of RNA sequencing and functional assays. We showed that activated Teff cells induce a specific transcriptomic program in MCs including production of both inflammatory cytokines and chemokines, prostaglandin, and a FcεRI-dependent degranulation facilitation, thereby driving them toward an inflammatory phenotype. Moreover, Teff cells induce in MCs the capacity to interact with CD4+ T cells through a wide range of dedicated soluble and membrane ligands and to play the role of antigen-presenting cells.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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