The microRNA miR-182 is induced by IL-2 and promotes clonal expansion of activated helper T lymphocytes
Author(s) -
AnnaBarbara Stittrich,
Claudia Haftmann,
Evridiki Sgouroudis,
Anja A. Kühl,
Ahmed N. Hegazy,
Isabel Panse,
René Riedel,
Michael Floßdorf,
Jun Dong,
Franziska Fuhrmann,
Gitta Anne Heinz,
Zhuo Fang,
Na Li,
Ute Bissels,
Farahnaz Hatam,
Angelina Jahn,
Ben Hammoud,
Mareen Matz,
Felix-Michael Schulze,
Ria Baumgrass,
Andreas Bosio,
HansJoachim Mollenkopf,
Joachim R. Grün,
Andreas Thiel,
Wei Chen,
Thomas Höfer,
Christoph Loddenkemper,
Max Löhning,
HyunDong Chang,
Nikolaus Rajewsky,
Andreas Radbruch,
MirFarzin Mashreghi
Publication year - 2010
Publication title -
nature immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.074
H-Index - 388
eISSN - 1529-2916
pISSN - 1529-2908
DOI - 10.1038/ni.1945
Subject(s) - foxo1 , biology , microrna , transcription factor , antigen , population , microbiology and biotechnology , t helper cell , immunology , interleukin 2 , immune system , t cell , cancer research , genetics , gene , medicine , environmental health
After being activated by antigen, helper T lymphocytes switch from a resting state to clonal expansion. This switch requires inactivation of the transcription factor Foxo1, a suppressor of proliferation expressed in resting helper T lymphocytes. In the early antigen-dependent phase of expansion, Foxo1 is inactivated by antigen receptor-mediated post-translational modifications. Here we show that in the late phase of expansion, Foxo1 was no longer post-translationally regulated but was inhibited post-transcriptionally by the interleukin 2 (IL-2)-induced microRNA miR-182. Specific inhibition of miR-182 in helper T lymphocytes limited their population expansion in vitro and in vivo. Our results demonstrate a central role for miR-182 in the physiological regulation of IL-2-driven helper T cell-mediated immune responses and open new therapeutic possibilities.
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