Monocyte-macrophages modulate intestinal homeostasis in inflammatory bowel disease
Authors:
Open Access
- 2 August 2024
- journal article
- review article
- Published by Springer Nature in Biomarker Research
- Vol. 12 (1) , 1-22
Abstract
Background: 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. Main body: 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. Conclusion: 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.Keywords
Funding Information
- National Natural Science Foundation of China (82300585, 82370532)
- Shanghai Sailing Program (23YF1432700)
This publication has 197 references indexed in Scilit:
- Macrophage plasticity, polarization, and function in health and diseaseJournal of Cellular Physiology, 2018
- Transcriptional Heterogeneity and Lineage Commitment in Myeloid ProgenitorsCell, 2015
- Crosstalk between Muscularis Macrophages and Enteric Neurons Regulates Gastrointestinal MotilityCell, 2014
- Resolution of inflammation: an integrated viewEMBO Molecular Medicine, 2013
- CD64 distinguishes macrophages from dendritic cells in the gut and reveals the Th1‐inducing role of mesenteric lymph node macrophages during colitisEuropean Journal of Immunology, 2012
- Regulatory macrophages induced by infliximab are involved in healing in vivo and in vitroInflammatory Bowel Diseases, 2012
- Elastin accumulation is regulated at the level of degradation by macrophage metalloelastase (MMP-12) during experimental liver fibrosisHepatology, 2011
- CX3CR1 defines functionally distinct intestinal mononuclear phagocyte subsets which maintain their respective functions during homeostatic and inflammatory conditionsEuropean Journal of Immunology, 2011
- Cellular and molecular mechanisms of fibrosisThe Journal of Pathology, 2007
- A significant part of macrophage-derived growth factor consists of at least two forms of PDGFCell, 1985