黏膜固有免疫细胞调节肠道稳态和肠道炎症。

Mucosal innate immune cells regulate both gut homeostasis and intestinal inflammation.

机构信息

Division of Mucosal Immunology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan; Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST), Tokyo, Japan; Division of Infectious Genetics, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

出版信息

Eur J Immunol. 2013 Dec;43(12):3108-15. doi: 10.1002/eji.201343782. Epub 2013 Oct 23.

Abstract

Continuous exposure of intestinal mucosal surfaces to diverse microorganisms and their metabolites reflects the biological necessity for a multifaceted, integrated epithelial and immune cell-mediated regulatory system. The development and function of the host cells responsible for the barrier function of the intestinal surface (e.g., M cells, Paneth cells, goblet cells, and columnar epithelial cells) are strictly regulated through both positive and negative stimulation by the luminal microbiota. Stimulation by damage-associated molecular patterns and commensal bacteria-derived microbe-associated molecular patterns provokes the assembly of inflammasomes, which are involved in maintaining the integrity of the intestinal epithelium. Mucosal immune cells located beneath the epithelium play critical roles in regulating both the mucosal barrier and the relative composition of the luminal microbiota. Innate lymphoid cells and mast cells, in particular, orchestrate the mucosal regulatory system to create a mutually beneficial environment for both the host and the microbiota. Disruption of mucosal homeostasis causes intestinal inflammation such as that seen in inflammatory bowel disease. Here, we review the recent research on the biological interplay among the luminal microbiota, epithelial cells, and mucosal innate immune cells in both healthy and pathological conditions.

摘要

肠道黏膜表面持续暴露于各种微生物及其代谢产物,反映出需要一个多方面的、综合的上皮细胞和免疫细胞介导的调节系统。负责肠道表面屏障功能的宿主细胞(如 M 细胞、潘氏细胞、杯状细胞和柱状上皮细胞)的发育和功能受到腔微生物的正向和负向刺激的严格调节。损伤相关分子模式和共生菌衍生的微生物相关分子模式的刺激会引发炎症小体的组装,这与维持肠道上皮细胞的完整性有关。位于上皮细胞下方的黏膜免疫细胞在调节黏膜屏障和腔微生物的相对组成方面发挥着关键作用。特别是固有淋巴细胞和肥大细胞,协调黏膜调节系统,为宿主和微生物创造互利的环境。黏膜稳态的破坏会导致肠道炎症,如炎症性肠病。在这里,我们综述了在健康和病理条件下,腔微生物、上皮细胞和黏膜固有免疫细胞之间的生物学相互作用的最新研究进展。

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