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前沿:滤泡辅助性 T 细胞发育过程中 BCL6 的表达呈现不同的波峰。

Cutting Edge: Distinct waves of BCL6 expression during T follicular helper cell development.

机构信息

Department of Microbiology and Immunology, Sandler Asthma Basic Research Center, University of California, San Francisco, San Francisco, CA 94143, USA.

出版信息

J Immunol. 2011 Sep 1;187(5):2089-92. doi: 10.4049/jimmunol.1101393. Epub 2011 Jul 29.

Abstract

T follicular helper (T(FH)) cells are central to the development and regulation of T cell-dependent humoral immune responses. The transcriptional repressor BCL6 is required for T(FH) responses, but the kinetics of BCL6 protein expression in activated CD4(+) T cells have not been established. We measured BCL6 expression during T(FH) cell development at the single-cell level using intracellular staining and YFP-BCL6 fusion protein reporter mice. BCL6 was immediately upregulated in all dividing T cells during dendritic cell-T cell interactions. A second wave of early BCL6 expression coincided with the induction of CXCR5, resulting in a distinct and stable T(FH) cell population. Cognate B cells were not required for the induction of BCL6, but supported the expansion of T(FH) cells. These data suggest that BCL6 participates in very early events in T(FH) cell development, and that repeated encounters with APCs reinforce BCL6 expression, thereby establishing the T(FH) cell phenotype.

摘要

滤泡辅助 T(T(FH))细胞是 T 细胞依赖性体液免疫应答发展和调节的核心。转录抑制因子 BCL6 是 T(FH) 应答所必需的,但激活的 CD4(+) T 细胞中 BCL6 蛋白表达的动力学尚未确定。我们使用细胞内染色和 YFP-BCL6 融合蛋白报告小鼠在单细胞水平上测量了 T(FH) 细胞发育过程中的 BCL6 表达。在树突状细胞与 T 细胞相互作用期间,BCL6 立即在所有分裂的 T 细胞中上调。第二波早期 BCL6 表达与 CXCR5 的诱导同时发生,导致形成一个独特且稳定的 T(FH)细胞群体。BCR 并非诱导 BCL6 所必需,但支持 T(FH)细胞的扩增。这些数据表明,BCL6 参与 T(FH) 细胞发育的早期事件,并且与 APC 的反复接触加强了 BCL6 的表达,从而建立了 T(FH)细胞表型。

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