Yang Congyi, Chen Jingyi, Zhao Yuzheng, Wu Jushan, Xu Yalan, Xu Jun, Chen Feng, Chen Yang, Chen Ning
Department of Gastroenterology, Peking University People's Hospital, Beijing 100044, China.
Central Laboratory, Peking University School of Stomatology, Beijing 100081, China.
iScience. 2024 Sep 27;27(11):111061. doi: 10.1016/j.isci.2024.111061. eCollection 2024 Nov 15.
Inflammatory bowel disease (IBD) presents a range of extraintestinal manifestations, notably including oral cavity involvement. The mechanisms underlying oral-gut crosstalk in IBD are not fully understood. Exosomes, found in various body fluids such as saliva, play an unclear role in IBD that requires further exploration. In the dextran sulfate sodium (DSS) mouse model, salivary exosomes from patients with active IBD (active IBD-Sexos) exacerbated colitis, while those from IBD patients in remission (remission IBD-Sexos) did not. Possible reasons may include the regulation of macrophage polarization, disruption of intestinal epithelial function, and alteration of the intestinal flora. During co-culture with active IBD-Sexos, THP-1 cells exhibited inflammatory responses, while Caco-2 cells showed reduced tight junction protein expression. Additionally, 35 differentially expressed miRNAs were identified in active IBD-Sexos. In brief, our findings substantiate an intriguing phenomenon whereby active IBD-Sexos exacerbate colitis by bridging the oral cavity and intestine.
炎症性肠病(IBD)会出现一系列肠外表现,尤其包括口腔受累。IBD中口腔与肠道相互作用的潜在机制尚未完全明确。在唾液等各种体液中发现的外泌体,在IBD中所起的作用尚不清楚,需要进一步探索。在葡聚糖硫酸钠(DSS)小鼠模型中,来自活动期IBD患者的唾液外泌体(活动期IBD-Sexos)会加重结肠炎,而来自缓解期IBD患者的唾液外泌体(缓解期IBD-Sexos)则不会。可能的原因包括巨噬细胞极化的调节、肠道上皮功能的破坏以及肠道菌群的改变。在与活动期IBD-Sexos共培养期间,THP-1细胞表现出炎症反应,而Caco-2细胞显示紧密连接蛋白表达降低。此外,在活动期IBD-Sexos中鉴定出35种差异表达的miRNA。简而言之,我们的研究结果证实了一个有趣的现象,即活动期IBD-Sexos通过连接口腔和肠道而加重结肠炎。