Yu Qing, Chang Hua-Chen, Ahyi Ayele-Nati N, Kaplan Mark H
Departments of Pediatrics, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
J Immunol. 2008 Sep 1;181(5):3346-52. doi: 10.4049/jimmunol.181.5.3346.
The IL-18Ralpha-chain is expressed on Th1 but not Th2 cells. We have recently shown that Stat4 is an important component of programming the Il18r1 locus (encoding IL-18Ralpha) for maximal expression in Th1 cells. Il18r1 is reciprocally repressed during Th2 development. In this report, we demonstrate the establishment of DH patterns that are distinct among undifferentiated CD4 T, Th1, and Th2 cells. Stat6 is required for the repression of Il18r1 expression and in Stat6-deficient Th2 cultures, mRNA levels, histone acetylation, and H3K4 methylation levels are intermediate between levels observed in Th1 and Th2 cells. Despite the repressive effects of IL-4 during Th2 differentiation, we observed only modest binding of Stat6 to the Il18r1 locus. In contrast, we observed robust GATA-3 binding to a central region of the locus where DNase hypersensitivity sites overlapped with conserved non-coding sequences in Il18r1 introns. Ectopic expression of GATA-3 in differentiated Th1 cells repressed Il18r1 mRNA and surface expression of IL-18Ralpha. These data provide further mechanistic insight into transcription factor-dependent establishment of Th subset-specific patterns of gene expression.
IL-18Rα链在Th1细胞而非Th2细胞上表达。我们最近发现,Stat4是在Th1细胞中对Il18r1基因座(编码IL-18Rα)进行编程以实现最大表达的重要组成部分。在Th2细胞发育过程中,Il18r1受到反向抑制。在本报告中,我们展示了在未分化的CD4 T细胞、Th1细胞和Th2细胞中存在不同的DH模式。Stat6是抑制Il18r1表达所必需的,在Stat6缺陷的Th2细胞培养物中,mRNA水平、组蛋白乙酰化和H3K4甲基化水平介于Th1细胞和Th2细胞中观察到的水平之间。尽管IL-4在Th2分化过程中有抑制作用,但我们仅观察到Stat6与Il18r1基因座有适度结合。相反,我们观察到GATA-3与该基因座的一个中心区域有强烈结合,该区域的DNase超敏位点与Il18r1内含子中的保守非编码序列重叠。在分化的Th1细胞中异位表达GATA-3可抑制Il18r1 mRNA和IL-18Rα的表面表达。这些数据为转录因子依赖性建立Th亚群特异性基因表达模式提供了进一步的机制性见解。