抄録
Regulatory T cells (T reg cells), which have abundant expression of the interleukin 2 receptor (IL-2R), are reliant on IL-2 produced by activated T cells. This feature indicates a key role for a simple network based on the consumption of IL-2 by T reg cells in their suppressor function. However, congenital deficiency in IL-2R results in reduced expression of the T reg cell lineage-specification factor Foxp3, which has confounded experimental efforts to understand the role of IL-2R expression and signaling in the suppressor function of T reg cells. Using genetic gain- and loss-of-function approaches, we found that capture of IL-2 was dispensable for the control of CD4 + T cells but was important for limiting the activation of CD8 + T cells, and that IL-2R-dependent activation of the transcription factor STAT5 had an essential role in the suppressor function of T reg cells separable from signaling via the T cell antigen receptor.
本文言語 | 英語 |
---|---|
ページ(範囲) | 1322-1333 |
ページ数 | 12 |
ジャーナル | Nature Immunology |
巻 | 17 |
号 | 11 |
DOI | |
出版ステータス | 出版済み - 10月 19 2016 |
外部発表 | はい |
!!!All Science Journal Classification (ASJC) codes
- 免疫アレルギー学
- 免疫学