Singapore Immunology Network, Agency for Science, Technology and Research, 8A Biomedical Grove, Singapore, 138648, Republic of Singapore.
Bioprocessing Technology Institute, Agency for Science, Technology and Research, 20 Biopolis Way, Singapore, 138668, Republic of Singapore.
Cell Death Dis. 2021 Nov 6;12(11):1054. doi: 10.1038/s41419-021-04357-5.
How pathogenesis of inflammatory bowel disease (IBD) depends on the complex interplay of host genetics, microbiome and the immune system is not fully understood. Here, we showed that Downstream of Kinase 3 (DOK3), an adapter protein involved in immune signaling, confers protection of mice from dextran sodium sulfate (DSS)-induced colitis. DOK3-deficiency promotes gut microbial dysbiosis and enhanced colitis susceptibility, which can be reversed by the transfer of normal microbiota from wild-type mice. Mechanistically, DOK3 exerts its protective effect by suppressing JAK2/STAT3 signaling in colonic neutrophils to limit their S100a8/9 production, thereby maintaining gut microbial ecology and colon homeostasis. Hence, our findings reveal that the immune system and microbiome function in a feed-forward manner, whereby DOK3 maintains colonic neutrophils in a quiescent state to establish a gut microbiome essential for intestinal homeostasis and protection from IBD.
炎症性肠病(IBD)的发病机制如何取决于宿主遗传学、微生物组和免疫系统的复杂相互作用尚不完全清楚。在这里,我们表明,参与免疫信号转导的衔接蛋白下游激酶 3(DOK3)赋予了小鼠对葡聚糖硫酸钠(DSS)诱导的结肠炎的保护作用。DOK3 缺陷促进肠道微生物失调和增强的结肠炎易感性,而从野生型小鼠中转移正常微生物群可以逆转这种情况。从机制上讲,DOK3 通过抑制结肠中性粒细胞中的 JAK2/STAT3 信号来发挥其保护作用,从而限制其 S100a8/9 的产生,从而维持肠道微生物生态和结肠内稳态。因此,我们的研究结果表明,免疫系统和微生物组以正反馈的方式发挥作用,DOK3 使结肠中性粒细胞保持静止状态,从而建立了对肠道内稳态和免受 IBD 保护至关重要的肠道微生物组。