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Tcf1 和 Lef1 对于调节性 T 细胞的免疫抑制功能是必需的。

Tcf1 and Lef1 are required for the immunosuppressive function of regulatory T cells.

机构信息

Departments of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, IA.

Guangdong Key Laboratory of Regional Immunity and Diseases, Department of Pathogen Biology, Shenzhen University School of Medicine, Shenzhen, Guangdong, China.

出版信息

J Exp Med. 2019 Apr 1;216(4):847-866. doi: 10.1084/jem.20182010. Epub 2019 Mar 5.

DOI:10.1084/jem.20182010
PMID:30837262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6446865/
Abstract

Tcf1 and Lef1 have versatile functions in regulating T cell development and differentiation, but intrinsic requirements for these factors in regulatory T (T reg) cells remain to be unequivocally defined. Specific ablation of Tcf1 and Lef1 in T reg cells resulted in spontaneous multi-organ autoimmunity that became more evident with age. Tcf1/Lef1-deficient T regs showed reduced protection against experimentally induced colitis, indicative of diminished immuno-suppressive capacity. Transcriptomic analysis revealed that Tcf1 and Lef1 were responsible for positive regulation of a subset of T reg-overrepresented signature genes such as and Unexpectedly, Tcf1 and Lef1 were necessary for restraining expression of cytotoxic CD8 effector T cell-associated genes in T reg cells, including and Tcf1 ChIP-seq revealed substantial overlap between Tcf1 and Foxp3 binding peaks in the T reg cell genome, with Tcf1-Foxp3 cooccupancy observed at key T reg signature and cytotoxic effector genes. Our data collectively indicate that Tcf1 and Lef1 are critical for sustaining T reg suppressive functions and preventing loss of self-tolerance.

摘要

Tcf1 和 Lef1 在调节 T 细胞发育和分化方面具有多种功能,但这些因子在调节性 T(Treg)细胞中的内在需求仍有待明确界定。Treg 细胞中 Tcf1 和 Lef1 的特异性缺失导致自发性多器官自身免疫,随着年龄的增长变得更加明显。Tcf1/Lef1 缺陷的 Treg 细胞对实验诱导的结肠炎的保护作用降低,表明其免疫抑制能力下降。转录组分析显示,Tcf1 和 Lef1 负责正向调节 Treg 细胞中一组代表性基因的表达,如和 。出乎意料的是,Tcf1 和 Lef1 对于抑制 Treg 细胞中细胞毒性 CD8 效应 T 细胞相关基因的表达是必需的,包括和 。Tcf1 ChIP-seq 显示 Tcf1 和 Foxp3 在 Treg 细胞基因组中的结合峰有大量重叠,在关键的 Treg 特征和细胞毒性效应基因上观察到 Tcf1-Foxp3 共占据。我们的数据表明,Tcf1 和 Lef1 对于维持 Treg 抑制功能和防止自身耐受的丧失至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/07f599bb638e/JEM_20182010_Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/9bf9feffd66a/JEM_20182010_GA.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/1268e359f9d2/JEM_20182010_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/c6a564d7b236/JEM_20182010_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/71873117a9d9/JEM_20182010_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/a1bb118dd07c/JEM_20182010_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/1d6625bc8a50/JEM_20182010_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/404a95387d5c/JEM_20182010_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/92f52bf22e29/JEM_20182010_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/07f599bb638e/JEM_20182010_Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/9bf9feffd66a/JEM_20182010_GA.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/1268e359f9d2/JEM_20182010_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/c6a564d7b236/JEM_20182010_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/71873117a9d9/JEM_20182010_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/a1bb118dd07c/JEM_20182010_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/1d6625bc8a50/JEM_20182010_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/404a95387d5c/JEM_20182010_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/92f52bf22e29/JEM_20182010_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/511c/6446865/07f599bb638e/JEM_20182010_Fig8.jpg

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