Gut microbiota‐derived tryptophan indole metabolites ameliorate collagen‐induced arthritis in mice via aryl hydrocarbon receptor activation in T cells and intestinal epithelial cells
作者
Liang Wu,Qiuping Zhang,Zhi-Gang Tang,Yanhong Li,Tong Wu,Lvyi Chen,Chunyu Tan,Lingshu Zhang,Xing Ji,Sijun Zhang,Yinlan Wu,Aline Bozec,Mario M. Zaiss,Yubin Luo
Objective To investigate the specific role of tryptophan metabolism, especially that of microbiome‐derived metabolites, in the development of rheumatoid arthritis (RA). Methods We employed metabolomics to profile metabolites in 53 high‐risk for RA individuals (PreRAs), 30 established RA patients and 38 healthy individuals. Fecal microbiota transplantation (FMT) and collagen‐induced arthritis (CIA) mouse models were used to investigate the impact of gut microbiome on arthritis severity, gut barrier function, and metabolic change. Treg cell differentiation and epithelial cells’ barrier function were assessed by flow cytometry, immunofluoresence staining and western blotting. Co‐immunoprecipitation and luciferase were applied for molecular mechanism studies. Results Dysregulated tryptophan metabolism exists in RA and PreRA individuals, as well as in FMT mice, characterized by a shift toward the kynurenine pathway and reduced activity of serotonin and indole pathways. Indole‐3‐lactic acid (ILA) and indole‐3‐acetic acid (IAA) significantly alleviated arthritis in CIA mice by expanding Treg cells via the classical aryl hydrocarbon receptor (AhR)‐aryl hydrocarbon receptor nuclear translocator (ARNT)‐xenobiotic response element (XRE) signaling pathway. Moreover, ILA repaired the leaking gut by increasing Zo‐1 and occludin expression in Caco‐2 cells, which was blocked by AhR antagonist CH223191. Moreover, CH223191 treatment could significantly reverse the improving effects of ILA and IAA on arthritis in mice. Conclusion These findings indicate that Trp indole metabolites may play a negative regulatory role in the progression of RA by affecting Treg cell development and intestinal gut barrier function.