Hofmann S R, Möller J, Rauen T, Paul D, Gahr M, Rösen-Wolff Z, Brenner S, Hedrich C M
Klinik und Poliklinik für Kinder- und Jugendmedizin, Neonatologie und Intensivmedizin, Dresden, Germany.
Klin Padiatr. 2012 Mar;224(2):53-60. doi: 10.1055/s-0031-1291359. Epub 2011 Dec 20.
The IL-10 family of cytokines consists of 9 members, including the immune-regulatory IL-10; Il19 is in close physical relationship with Il10 in the so-called IL-10 cytokine cluster on chromosome 1q32. While IL-10 is ubiquitously expressed, IL-19 expression is restricted to myeloid and epithelial cells. Little is known about molecular mechanisms that control tissue-specific expression of IL-10, and IL-19. Modifications in CpG-DNA methylation are a key mechanism in controlling transcription. Using bisulfite sequencing, we demonstrate that murine Il19 is methylated in CD4+ T lymphocytes. Macrophages display site-specific demethylation of Il19. The ubiquitously expressed Il10 gene is methylated to a lower degree and exhibits tissue-specific methylation patterns. DNA demethylation with 5-azacytidine resulted in an induction of IL-10, and IL-19 expression in CD4+ T cells, and CpG-DNA methylation through DNMT3a resulted in transcriptional silencing in macrophages. Thus, our findings suggest a role of CpG-DNA methylation in the regulation of Il10 and Il19.
白细胞介素-10(IL-10)细胞因子家族由9个成员组成,包括免疫调节性的IL-10;IL-19与IL-10在1号染色体1q32上所谓的IL-10细胞因子簇中在物理位置上紧密相关。虽然IL-10在全身广泛表达,但IL-19的表达局限于髓样细胞和上皮细胞。关于控制IL-10和IL-19组织特异性表达的分子机制知之甚少。CpG-DNA甲基化修饰是控制转录的关键机制。通过亚硫酸氢盐测序,我们证明小鼠的Il19在CD4 + T淋巴细胞中发生甲基化。巨噬细胞显示出Il19的位点特异性去甲基化。广泛表达的Il10基因甲基化程度较低,并呈现出组织特异性甲基化模式。用5-氮杂胞苷进行DNA去甲基化导致CD4 + T细胞中IL-10和IL-19的表达诱导,而通过DNA甲基转移酶3a(DNMT3a)进行的CpG-DNA甲基化导致巨噬细胞中的转录沉默。因此,我们的研究结果表明CpG-DNA甲基化在Il10和Il19的调节中起作用。