Department of Immunology, School of Medicine, Wuhan University, Wuhan, China.
Department of Pharmacology, School of Medicine, Wuhan University, Wuhan, China.
Scand J Immunol. 2018 Sep;88(3):e12701. doi: 10.1111/sji.12701. Epub 2018 Aug 16.
Interleukin (IL)-10 is an essential anti-inflammatory cytokine that plays important roles as a negative regulator of immune responses to microbial antigens. c-Maf has been suggested as an essential transcriptional factor for IL-10 production in CD4 T cells and macrophages. However, it remains unclear whether c-Maf participates in IL-10 expression in B cells. In this study, we investigated the role of c-Maf in the transcriptional regulation of IL-10 in regulatory B cells, as well as the underlying molecular mechanism. We found that c-Maf was constitutively expressed in resting B cells. c-Maf expression was upregulated in the presence of LPS and dose-dependently enhanced IL-10 production following binding to the IL-10 promoter. Moreover, a lower expression of c-Maf and decreased production of regulatory B (Breg) cells were detected in mice with collagen-induced arthritis (CIA), which may contribute to the pathological changes. Taken together, these data demonstrate that c-Maf is an indispensable yet constitutive transcription factor for IL-10 gene expression in LPS-activated B cells.
白细胞介素 (IL)-10 是一种重要的抗炎细胞因子,作为微生物抗原免疫反应的负调节剂发挥重要作用。c-Maf 被认为是 CD4 T 细胞和巨噬细胞中 IL-10 产生的必需转录因子。然而,c-Maf 是否参与 B 细胞中 IL-10 的表达仍不清楚。在这项研究中,我们研究了 c-Maf 在调节性 B 细胞中 IL-10 转录调控中的作用,以及潜在的分子机制。我们发现 c-Maf 在静止的 B 细胞中持续表达。LPS 的存在可上调 c-Maf 的表达,并与 IL-10 启动子结合后,剂量依赖性地增强 IL-10 的产生。此外,在胶原诱导性关节炎 (CIA) 小鼠中,c-Maf 的表达水平较低,调节性 B(Breg)细胞的产生减少,这可能导致病理变化。总之,这些数据表明 c-Maf 是 LPS 激活的 B 细胞中 IL-10 基因表达所必需的组成性转录因子。