151. Increased level of E protein activity during iNKT development promotes differentiation of iNKT2 and iNKT17 subsets
- Author
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Hu, Taishan, Wang, Hongcheng, Simmons, Amie, Bajaña, Sandra, Zhao, Ying, Kovats, Susan, Sun, Xiao-hong, and Alberola-Ila, Jose
- Subjects
RNA, Untranslated ,Cell Differentiation ,Mice, Transgenic ,Lymphocyte Activation ,Article ,Lymphocyte Subsets ,Interleukin-2 Receptor beta Subunit ,Mice, Inbred C57BL ,Interferon-gamma ,Mice ,Core Binding Factor Alpha 3 Subunit ,Basic Helix-Loop-Helix Transcription Factors ,Animals ,Natural Killer T-Cells ,T-Box Domain Proteins ,Cells, Cultured ,Cell Proliferation ,Signal Transduction - Abstract
E protein transcription factors and their natural inhibitors, Id proteins, play critical and complex roles during lymphoid development. In this article, we report that partial maintenance of E protein activity during positive selection results in a change in the cell fate determination of developing iNKT cells, with a block in the development of iNKT1 cells and a parallel increase in the iNKT2 and iNKT17 subsets. Because the expression levels of the transcription factors that drive these alternative functional fates (GATA-3, RORγT, T-bet, and Runx-3) are not altered, our results suggest that E protein activity controls a novel checkpoint that regulates the number of iNKT precursors that choose each fate.
- Published
- 2013