Lu Huiying, Suo Zhimin, Lin Jian, Cong Yingzi, Liu Zhanju
Department of Gastroenterology, Huaihe Hospital of Henan University, Henan Province, Kaifeng, 475000, China.
Center for Inflammatory Bowel Disease Research and Department of Gastroenterology, Shanghai Tenth People's Hospital of Tongji University, No. 301 Yanchang Road, Shanghai, 200072, China.
Biomark Res. 2024 Aug 2;12(1):76. doi: 10.1186/s40364-024-00612-x.
Monocytes and macrophages play an indispensable role in maintaining intestinal homeostasis and modulating mucosal immune responses in inflammatory bowel disease (IBD). Although numerous studies have described macrophage properties in IBD, the underlying mechanisms whereby the monocyte-macrophage lineage modulates intestinal homeostasis during gut inflammation remain elusive.
In this review, we decipher the cellular and molecular mechanisms governing the generation of intestinal mucosal macrophages and fill the knowledge gap in understanding the origin, maturation, classification, and functions of mucosal macrophages in intestinal niches, particularly the phagocytosis and bactericidal effects involved in the elimination of cell debris and pathogens. We delineate macrophage-mediated immunoregulation in the context of producing pro-inflammatory and anti-inflammatory cytokines, chemokines, toxic mediators, and macrophage extracellular traps (METs), and participating in the modulation of epithelial cell proliferation, angiogenesis, and fibrosis in the intestine and its accessory tissues. Moreover, we emphasize that the maturation of intestinal macrophages is arrested at immature stage during IBD, and the deficiency of MCPIP1 involves in the process via ATF3-AP1S2 signature. In addition, we confirmed the origin potential of IL-1B macrophages and defined C1QB macrophages as mature macrophages. The interaction crosstalk between the intestine and the mesentery has been described in this review, and the expression of mesentery-derived SAA2 is upregulated during IBD, which contributes to immunoregulation of macrophage. Moreover, we also highlight IBD-related susceptibility genes (e.g., RUNX3, IL21R, GTF2I, and LILRB3) associated with the maturation and functions of macrophage, which provide promising therapeutic opportunities for treating human IBD.
In summary, this review provides a comprehensive, comprehensive, in-depth and novel description of the characteristics and functions of macrophages in IBD, and highlights the important role of macrophages in the molecular and cellular process during IBD.
单核细胞和巨噬细胞在维持肠道稳态以及调节炎症性肠病(IBD)中的黏膜免疫反应方面发挥着不可或缺的作用。尽管众多研究已描述了IBD中巨噬细胞的特性,但在肠道炎症期间单核细胞 - 巨噬细胞谱系调节肠道稳态的潜在机制仍不清楚。
在本综述中,我们解读了调控肠道黏膜巨噬细胞生成的细胞和分子机制,并填补了在理解肠道微环境中黏膜巨噬细胞的起源、成熟、分类及功能方面的知识空白,特别是涉及清除细胞碎片和病原体的吞噬作用及杀菌作用。我们阐述了巨噬细胞在产生促炎和抗炎细胞因子、趋化因子、毒性介质以及巨噬细胞胞外陷阱(METs)的背景下介导的免疫调节作用,以及参与调节肠道及其附属组织中的上皮细胞增殖、血管生成和纤维化。此外,我们强调在IBD期间肠道巨噬细胞的成熟停滞在未成熟阶段,并且MCPIP1的缺乏通过ATF3 - AP1S2信号通路参与该过程。另外,我们证实了IL - 1B巨噬细胞的起源潜能,并将C1QB巨噬细胞定义为成熟巨噬细胞。本综述描述了肠道与肠系膜之间的相互作用,并且在IBD期间肠系膜来源的SAA2表达上调,这有助于巨噬细胞的免疫调节。此外,我们还强调了与巨噬细胞成熟和功能相关的IBD相关易感基因(例如RUNX3、IL21R、GTF2I和LILRB3),这为治疗人类IBD提供了有前景的治疗机会。
总之,本综述对IBD中巨噬细胞的特征和功能进行了全面、深入且新颖的描述,并突出了巨噬细胞在IBD期间分子和细胞过程中的重要作用。