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Bcl6 表达在体内特异性规定滤泡辅助性 T 细胞程序。

Bcl6 expression specifies the T follicular helper cell program in vivo.

机构信息

Department of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Exp Med. 2012 Sep 24;209(10):1841-52, S1-24. doi: 10.1084/jem.20120219. Epub 2012 Sep 17.

DOI:10.1084/jem.20120219
PMID:22987803
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3457730/
Abstract

T follicular helper cells (Tfh cells) play a pivotal role in germinal center reactions, which require B cell lymphoma 6 (Bcl6) transcription factor. To analyze their relationships with other effector T cell lineages and their stability in vivo, we developed and analyzed a new Bcl6 reporter mouse alone or together with other lineage reporter systems. Assisted with genome-wide transcriptome analysis, we show substantial plasticity of T cell differentiation in the early phase of immune response. At this stage, CXCR5 appears to be expressed in a Bcl6-independent manner. Once Bcl6 is highly expressed, Tfh cells can persist in vivo and some of them develop into memory cells. Together, our results indicate Bcl6 as a bona fide marker for Tfh polarized program.

摘要

滤泡辅助性 T 细胞(Tfh 细胞)在生发中心反应中发挥关键作用,生发中心反应需要 B 细胞淋巴瘤 6(Bcl6)转录因子。为了分析它们与其他效应 T 细胞谱系的关系及其在体内的稳定性,我们单独或与其他谱系报告系统一起开发和分析了一种新的 Bcl6 报告小鼠。通过全基因组转录组分析,我们显示了免疫反应早期 T 细胞分化的巨大可塑性。在这个阶段,CXCR5 似乎以 Bcl6 独立的方式表达。一旦 Bcl6 高度表达,Tfh 细胞就可以在体内持续存在,其中一些细胞发育成记忆细胞。总之,我们的结果表明 Bcl6 是 Tfh 极化程序的真正标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/ff72a86615ea/JEM_20120219_Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/d222f3b19543/JEM_20120219_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/317a60815d26/JEM_20120219_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/bd45b68812af/JEM_20120219R_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/6d0e50a8bc38/JEM_20120219_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/9b2ee4c561b1/JEM_20120219_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/e55c63d6ab85/JEM_20120219_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/94edac5c1dc3/JEM_20120219_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/ff72a86615ea/JEM_20120219_Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/d222f3b19543/JEM_20120219_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/317a60815d26/JEM_20120219_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/bd45b68812af/JEM_20120219R_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/6d0e50a8bc38/JEM_20120219_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/9b2ee4c561b1/JEM_20120219_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/e55c63d6ab85/JEM_20120219_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/94edac5c1dc3/JEM_20120219_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9606/3457730/ff72a86615ea/JEM_20120219_Fig8.jpg

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Functional and epigenetic studies reveal multistep differentiation and plasticity of in vitro-generated and in vivo-derived follicular T helper cells.
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