| Literature DB >> 28586108 |
Markus M Xie1, Byung-Hee Koh1,2, Kristin Hollister1, Hao Wu1, Jie Sun1,2, Mark H Kaplan1,2, Alexander L Dent1.
Abstract
The transcription factors Bcl6 and Blimp1 have opposing roles in the development of the follicular helper T (TFH ) cells: Bcl6 promotes and Blimp1 inhibits TFH -cell differentiation. Similarly, Bcl6 activates, while Blimp1 represses, expression of the TFH -cell marker PD-1. However, Bcl6 and Blimp1 repress each other's expression, complicating the interpretation of the regulatory network. Here we sought to clarify the extent to which Bcl6 and Blimp1 independently control TFH -cell differentiation by generating mice with T-cell specific deletion of both Bcl6 and Blimp1 (double conditional KO [dcKO] mice). Our data indicate that Blimp1 does not control TFH -cell differentiation independently of Bcl6. However, a population of T follicular regulatory (TFR ) cells developed independently of Bcl6 in dcKO mice. We have also analyzed regulation of IL-10 and PD-1, two genes controlled by both Bcl6 and Blimp1, and observed that Bcl6 regulates both genes independently of Blimp1. We found that Bcl6 positively regulates PD-1 expression by inhibiting the ability of T-bet/Tbx21 to repress Pdcd1 transcription. Our data provide a novel mechanism for positive control of gene expression by Bcl6, and illuminate how Bcl6 and Blimp1 control TFH -cell differentiation.Entities:
Keywords: Bcl6; Blimp1; Follicular helper T cells; Germinal center; PD-1; T follicular regulatory cells; T-bet
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Year: 2017 PMID: 28586108 PMCID: PMC5578616 DOI: 10.1002/eji.201747034
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532