肠道菌群
免疫系统
生物
先天性淋巴细胞
免疫学
细胞生物学
平衡
先天免疫系统
趋化因子
白细胞介素22
细胞因子
白细胞介素
作者
Wei Chen,Dan Liu,Changhao Ren,Lei Su,Chun Kwok Wong,Rongcun Yang
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2022-01-17
卷期号:11 (2): 307-307
被引量:18
标识
DOI:10.3390/cells11020307
摘要
A number of gut epithelial cells derived immunological factors such as cytokines and chemokines, which are stimulated by the gut microbiota, can regulate host immune responses to maintain a well-balance between gut microbes and host immune system. Multiple specialized immune cell populations, such as macrophages, dendritic cells (DCs), innate lymphoid cells, and T regulatory (Treg) cells, can communicate with intestinal epithelial cells (IEC) and/or the gut microbiota bi-directionally. The gut microbiota contributes to the differentiation and function of resident macrophages. Situated at the interface between the gut commensals and macrophages, the gut epithelium is crucial for gut homeostasis in microbial recognition, signaling transformation, and immune interactions, apart from being a physical barrier. Thus, three distinct but interactive components-macrophages, microbiota, and IEC-can form a network for the delicate and dynamic regulation of intestinal homeostasis. In this review, we will discuss the crucial features of gut microbiota, macrophages, and IEC. We will also summarize recent advances in understanding the cooperative and dynamic interactions among the gut microbiota, gut macrophages, and IEC, which constitute a special network for gut homeostasis.
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