Xu Huihui, Cao Jinfeng, Li Xiaoya, Lu Xiangchen, Xia Ya, Fan Danping, Zhao Hongyan, Ju Dahong, Xiao Cheng
Beijing Key Laboratory of Research of Chinese Medicine on Prevention and Treatment for Major Diseases, Experimental Research Center, China Academy of Chinese Medical Science, Beijing, China.
Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China.
Front Pharmacol. 2020 Nov 24;11:587534. doi: 10.3389/fphar.2020.587534. eCollection 2020.
Rheumatoid arthritis (RA) is a common autoimmune disease characterized by chronic inflammation and a multifactorial etiology. We previously showed that gut microbiota dysbiosis in the rat ileum is involved in the development of collagen-induced arthritis (CIA). The gut microbiota in the distinct gastrointestinal tract (GIT) plays region-specific roles, but information on the different roles of the microbiota in distinct GIT compartments of CIA rats is limited. This study aimed to evaluate the region-specific differences in the gut microbial communities and certain gut-associated immunologic factors in the ileum and cecum of CIA rats. Ileal and cecal digesta were collected from CIA and control rats for microbiome analysis. We determined the microbial richness, diversity and taxa as well as the expression of interleukin (IL)-1β and IL-17A in the epithelium and lamina propria of the ileum and cecum mucosal layers. The CIA-induced microbiota alterations in the ileum differed from those in the cecum. The ileal microbiota were more markedly influenced in CIA, as revealed by sharp reductions in the abundances of the families Enterococcaceae, Lactobacillaceae and Streptococcaceae and the genera and Moreover, significant increases in IL-1β, and IL-17A mRNA expression were detected in only the ileal epithelium and lamina propria of the mucosal layer. Therefore, the microbial characteristics in the ileum were consistent with the immune-mediated inflammatory features of CIA, suggesting that the ileal microbiota might better represent the CIA-induced inflammatory responses than the cecal microbiota and that these responses might partially impact the progression of RA by regulating intestinal mucosal immunity.
类风湿性关节炎(RA)是一种常见的自身免疫性疾病,其特征为慢性炎症和多因素病因。我们之前表明,大鼠回肠中的肠道微生物群失调与胶原诱导的关节炎(CIA)的发展有关。不同胃肠道(GIT)中的肠道微生物群发挥着区域特异性作用,但关于CIA大鼠不同GIT区域中微生物群不同作用的信息有限。本研究旨在评估CIA大鼠回肠和盲肠中肠道微生物群落以及某些肠道相关免疫因子的区域特异性差异。从CIA大鼠和对照大鼠收集回肠和盲肠内容物用于微生物组分析。我们测定了微生物的丰富度、多样性和分类群,以及回肠和盲肠黏膜层上皮和固有层中白细胞介素(IL)-1β和IL-17A的表达。CIA诱导的回肠微生物群改变与盲肠不同。CIA对回肠微生物群的影响更为明显,表现为肠球菌科、乳杆菌科和链球菌科以及相关属的丰度急剧下降。此外,仅在黏膜层的回肠上皮和固有层中检测到IL-1β和IL-17A mRNA表达显著增加。因此,回肠中的微生物特征与CIA的免疫介导炎症特征一致,表明回肠微生物群可能比盲肠微生物群更能代表CIA诱导的炎症反应,并且这些反应可能通过调节肠道黏膜免疫部分影响RA的进展。