Tsinghua-Peking Joint Center for Life Sciences, Tsinghua University School of Medicine, Beijing 100084, China.
Tsinghua-Peking Joint Center for Life Sciences, Tsinghua University School of Medicine, Beijing 100084, China.
Cell Rep. 2015 Nov 10;13(6):1149-1160. doi: 10.1016/j.celrep.2015.09.073.
Dendritic cells (DCs) and macrophages play important roles in maintaining intestinal homeostasis. However, the molecular mechanisms that regulate the differentiation and responses of intestinal DCs and macrophages remain poorly understood. Here, we have identified microRNA miR-223 as a key molecule for regulating these processes. Deficiency of miR-223 led to a significantly decreased number of intestinal CX3CR1(hi) macrophages at steady state. Both intestinal CX3CR1(hi) macrophages and CD103(+) conventional DCs (cDCs) in miR-223-deficient mice exhibited a strong pro-inflammatory phenotype. Moreover, miR-223-deficient monocytes gave rise to more monocyte-derived DCs (moDCs) and produced more pro-inflammatory cytokines upon stimulation. Using a mouse model of colitis, we demonstrated that the miR-223 deficiency resulted in more severe colitis. Target gene analysis further identified that the effects of miR-223 on DCs and macrophages were mediated by directly targeting C/EBPβ. Taken together, our study identifies a role for miR-223 as a critical regulator of intestinal homeostasis.
树突状细胞 (DCs) 和巨噬细胞在维持肠道内稳态方面发挥着重要作用。然而,调节肠道 DCs 和巨噬细胞分化和反应的分子机制仍知之甚少。在这里,我们鉴定出 microRNA miR-223 是调节这些过程的关键分子。miR-223 缺陷导致稳定状态下肠道 CX3CR1(hi) 巨噬细胞数量显著减少。miR-223 缺陷小鼠的肠道 CX3CR1(hi) 巨噬细胞和 CD103(+) 常规 DCs (cDCs) 均表现出强烈的促炎表型。此外,miR-223 缺陷单核细胞在刺激后产生更多的单核细胞衍生的 DCs (moDCs) 并产生更多的促炎细胞因子。利用结肠炎小鼠模型,我们证明了 miR-223 缺陷导致更严重的结肠炎。靶基因分析进一步表明,miR-223 对 DCs 和巨噬细胞的作用是通过直接靶向 C/EBPβ 介导的。总之,我们的研究确定了 miR-223 作为肠道内稳态关键调节因子的作用。