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T 细胞如何获得滤泡通行权。

How T cells earn the follicular rite of passage.

机构信息

Department of Pathogens and Immunity, John Curtin School of Medical Research, The Australian National University, Canberra, ACT 2601, Australia.

出版信息

Immunity. 2011 Nov 23;35(5):671-80. doi: 10.1016/j.immuni.2011.11.001.

Abstract

The discovery that Bcl-6 was the transcriptional regulator of follicular helper T (Tfh) cells completed the recognition of this population as an effector subset specialized in the provision of help to B cells. Improved reagents and recent models that allow tracking of Bcl-6-expressing T cells have revealed that the decision to become a Tfh cell occurs soon after T cells are primed by dendritic cells and start dividing, before interaction with B cells. The latter are important for sustaining Bcl-6 expression. Bcl-6 coordinates a signaling program that changes expression or function of multiple guidance receptors, leading to Tfh cell localization within germinal centers. This program is not unique to CD4(+) helper T cells; FoxP3(+) regulatory T cells and NKT cells co-opt the follicular differentiation pathway to enter the follicle and become specialized follicular cells. This review will focus on recent insights into the early events that determine Tfh cell differentiation.

摘要

Bcl-6 是滤泡辅助性 T(Tfh)细胞的转录调控因子这一发现,使人们完整地认识到 Tfh 细胞是一类专门为 B 细胞提供辅助的效应亚群。改良的试剂和最近的模型允许跟踪表达 Bcl-6 的 T 细胞,揭示了成为 Tfh 细胞的决定发生在 T 细胞被树突状细胞激活并开始分裂后不久,在与 B 细胞相互作用之前。后者对于维持 Bcl-6 的表达很重要。Bcl-6 协调了一个信号转导程序,改变了多个导向受体的表达或功能,导致 Tfh 细胞在生发中心内定位。这个程序并不是 CD4+辅助 T 细胞所特有的;FoxP3+调节性 T 细胞和 NKT 细胞也采用滤泡分化途径进入滤泡并成为专门的滤泡细胞。这篇综述将重点介绍最近对决定 Tfh 细胞分化的早期事件的深入了解。

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