Jeon Phil Hyun, Oh Kwon Ik
Department of Pathology, Hallym University College of Medicine, Chuncheon, Gangwon-Do, Korea.
Anim Cells Syst (Seoul). 2016 Dec 30;21(1):1-9. doi: 10.1080/19768354.2016.1272489. eCollection 2017.
Regulatory T cells (Tregs), specified by the expression of transcription factor Foxp3, operate Foxp3-dependent programs to maintain self-tolerance. In addition to Foxp3, other tissue-specific transcription factors are also required by Tregs to control the corresponding immune responses like follicular Tregs which express both Foxp3 and Bcl6 controlling germinal center reactions. Here, we show that Interleukin 2 (IL2) is required for the optimal expression of T helper type 1 (Th1) transcription factor T-box 21 (, T-bet) in Tregs. The expression levels of CXCR3 and T-bet were reduced in IL2 deficient Tregs. Furthermore, IL2 deficient Treg cells failed to control the proliferation of CD4 T cells and could not prevent the progression of colitis characterized by Th1 immune responses. Taken together, our data suggest that IL2 is essential for the functional maturation of Tregs including the optimal suppressive activity and the expression of tissue-specific transcription factors like T-bet.
调节性T细胞(Tregs)由转录因子Foxp3的表达所确定,其通过依赖Foxp3的程序来维持自身耐受性。除了Foxp3之外,Tregs还需要其他组织特异性转录因子来控制相应的免疫反应,如表达Foxp3和Bcl6的滤泡性Tregs控制生发中心反应。在此,我们表明白细胞介素2(IL2)是Tregs中1型辅助性T细胞(Th1)转录因子T盒21(T-bet)最佳表达所必需的。在IL2缺陷的Tregs中,CXCR3和T-bet的表达水平降低。此外,IL2缺陷的Treg细胞无法控制CD4 T细胞的增殖,并且不能预防以Th1免疫反应为特征的结肠炎进展。综上所述,我们的数据表明IL2对于Tregs的功能成熟至关重要,包括最佳抑制活性以及T-bet等组织特异性转录因子的表达。