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Bach2 负向调控滤泡辅助性 T 细胞分化,是 CD4 T 细胞记忆形成所必需的。

Bach2 Negatively Regulates T Follicular Helper Cell Differentiation and Is Critical for CD4 T Cell Memory.

机构信息

Department of Microbiology, School of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.

Department of Medicine, School of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294; and.

出版信息

J Immunol. 2019 May 15;202(10):2991-2998. doi: 10.4049/jimmunol.1801626. Epub 2019 Apr 10.

Abstract

T follicular helper (Tfh) cells are essential for germinal center B cell responses. The molecular mechanism underlying the initial Tfh cell differentiation, however, is still incompletely understood. In this study, we show that in vivo, despite enhanced non-Tfh cell effector functions, the deletion of transcription factor Bach2 results in preferential Tfh cell differentiation. Mechanistically, the deletion of Bach2 leads to the induction of CXCR5 expression even before the upregulation of Ascl2. Subsequently, we have identified a novel regulatory element in the murine CXCR5 locus that negatively regulates CXCR5 promoter activities in a Bach2-dependent manner. Bach2 deficiency eventually results in a collapsed CD4 T cell response with severely impaired CD4 T cell memory, including Tfh cell memory. Our results demonstrate that Bach2 critically regulates Tfh cell differentiation and CD4 T cell memory.

摘要

滤泡辅助 T(Tfh)细胞对于生发中心 B 细胞反应至关重要。然而,初始 Tfh 细胞分化的分子机制仍不完全清楚。在这项研究中,我们表明,尽管增强了非 Tfh 细胞的效应功能,但转录因子 Bach2 的缺失导致 Tfh 细胞的分化偏好。从机制上讲,Bach2 的缺失导致 CXCR5 表达的诱导,甚至在 Ascl2 的上调之前。随后,我们在小鼠 CXCR5 基因座中鉴定出一个新的调节元件,该元件以 Bach2 依赖性的方式负调控 CXCR5 启动子活性。Bach2 的缺乏最终导致 CD4 T 细胞反应崩溃,严重损害 CD4 T 细胞记忆,包括 Tfh 细胞记忆。我们的结果表明,Bach2 对 Tfh 细胞分化和 CD4 T 细胞记忆具有关键的调控作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5555/6504585/b9e00bcd25f0/nihms-1525290-f0001.jpg

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