细胞生物学
小RNA
CX3CR1型
调节器
结肠炎
平衡
炎症
生物
树突状细胞
化学
免疫学
趋化因子
免疫系统
基因
生物化学
趋化因子受体
作者
Haibo Zhou,Jing Xiao,Ning Wu,Chunxi Liu,Jie Xu,Fang Liu,Li Wu
出处
期刊:Cell Reports
[Cell Press]
日期:2015-11-01
卷期号:13 (6): 1149-1160
被引量:93
标识
DOI:10.1016/j.celrep.2015.09.073
摘要
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.
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