College of Food Science and Engineering, Jilin Agricultural University, Changchun 130118, Jilin, P. R. China.
National Engineering Laboratory of Wheat and Corn Deep Processing, Changchun 130118, Jilin, P. R. China.
J Agric Food Chem. 2022 Feb 23;70(7):2197-2210. doi: 10.1021/acs.jafc.1c06502. Epub 2022 Feb 4.
This study investigated the effects of the exopolysaccharide from JLAU103 (EPS103) on the intestinal immune response, oxidative stress, intestinal mucosal barrier, and microbial community in cyclophosphamide-induced immune-suppressed mice. The results showed that EPS103 promoted the secretion of cytokines and the generation of secretory immunoglobulin A and mucin-2 in the small intestine of mice, which might be related to the activation of the MAPK pathway. Additionally, EPS103 protected against oxidative stress by activating antioxidation enzymes and Nrf2/Keap1 pathways. It also improved the intestinal physical barrier functions regulating the ratio of villous height to crypt depth and upregulating the expression of tight-junction proteins. Meanwhile, EPS103 promoted the generation of short-chain fatty acids (SCFAs) and modulated the constituents of gut microbiota. These results suggested that EPS103 may modulate the intestinal immunoresponse relying on the regulation of SCFA production and gut microbiota in immunosuppressed mice, resulting in the activation of systemic immunity.
本研究考察了 JLAU103(EPS103)胞外多糖对环磷酰胺诱导免疫抑制小鼠肠道免疫应答、氧化应激、肠道黏膜屏障和微生物群落的影响。结果表明,EPS103 促进了小鼠小肠细胞因子的分泌以及分泌型免疫球蛋白 A 和粘蛋白-2 的产生,这可能与 MAPK 通路的激活有关。此外,EPS103 通过激活抗氧化酶和 Nrf2/Keap1 通路来抵抗氧化应激。它还通过调节绒毛高度与隐窝深度的比值和上调紧密连接蛋白的表达来改善肠道物理屏障功能。同时,EPS103 促进短链脂肪酸(SCFAs)的生成,并调节肠道微生物群落的组成。这些结果表明,EPS103 可能通过调节 SCFA 的产生和免疫抑制小鼠的肠道微生物群来调节肠道免疫应答,从而激活全身免疫。