4.5 Article

The Bcl6 target gene microRNA-21 promotes Th2 differentiation by a T cell intrinsic pathway

期刊

MOLECULAR IMMUNOLOGY
卷 54, 期 3-4, 页码 435-442

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.molimm.2013.01.006

关键词

MicroRNA; Bcl6; Th2 differentiation; Regulatory T cells

资金

  1. NIAID [1R21AI079349-01A1, 1R21AI090150-01, 1R21AI092212-01]
  2. American Heart Association pre-doctoral fellowship [10PRE4620001]

向作者/读者索取更多资源

The transcriptional repressor Bcl6 is a critical regulator of T helper cell fate, and inhibits Th2-type inflammation. We have found that microRNA-21 (miR-21) is a novel target gene for Bcl6 in Treg cells. Bcl6 represses and Stat3 activates miR-21 transcription through a Stat3 binding element in the promoter, indicating opposing regulation of miR-21 by the two transcription factors via the same DNA site. Ectopic expression of miR-21 promoted Th2 differentiation in non-polarized T cells. The pro-Th2 activity of miR21 was associated with increased Gata3 expression and decreased expression of the miR-21 target gene Sprouty1. Increased miR-21 promoted Th2 and Treg gene expression in wild-type Tregs. MiR-21 could thus help promote the Th2 bias of Bcl6-deficient conventional T cells and Treg cells. MiR-21 expression is increased in Th2-type inflammation, and our results define miR-21 as a critical target of Bcl6, thus providing a new link between Bcl6 and Th2 inflammation. Finally, our results reveal a novel T cell autonomous role for miR-21 in promoting Th2 differentiation. (C) 2013 Elsevier Ltd. All rights reserved.

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