Bcl6 expression specifies the T follicular helper cell program in vivo

Xindong Liu(The University of Texas MD Anderson Cancer Center), Xiaowei Yan(Institute for Systems Biology), Bo Zhong(The University of Texas MD Anderson Cancer Center), Roza Nurieva(The University of Texas MD Anderson Cancer Center), Aibo Wang(The University of Texas MD Anderson Cancer Center), Xiaohu Wang(The University of Texas MD Anderson Cancer Center), Natalia Martín‐Orozco(The University of Texas MD Anderson Cancer Center), Yihong Wang(The University of Texas MD Anderson Cancer Center), Seon Hee Chang(The University of Texas MD Anderson Cancer Center), Enric Esplugues(Howard Hughes Medical Institute), Richard A. Flavell(Howard Hughes Medical Institute), Qiang Tian(Institute for Systems Biology), Chen Dong(The University of Texas MD Anderson Cancer Center)
The Journal of Experimental Medicine
September 17, 2012
Cited by 265Open Access
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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.


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