Guangdong Provincial Key Laboratory of Lingnan Specialty Food Science and Technology, Guangzhou City, Guangdong 510642, China.
College of Light Industry and Food, Zhongkai University of Agriculture and Engineering, Guangzhou, Guangdong 510225, China.
J Agric Food Chem. 2021 Nov 17;69(45):13510-13523. doi: 10.1021/acs.jafc.1c05134. Epub 2021 Nov 5.
polysaccharide (DOP) attenuates inflammatory bowel disease (IBD), but its role in regulating cross-talk between intestinal epithelial cells (IEC) and macrophages against IBD is unclear. This study aimed to investigate DOP protective effects on the intestinal inflammatory response through regulation by miRNA in small extracellular vesicles (sEVs). Our results show that DOP interfered with the secretion of small extracellular vesicles (DIEs) by IEC, which reduced the levels of inflammatory mediators. Increased miR-433-3p expression in DIEs was identified as an important protector against intestinal inflammation. DOP regulated the loading of miR-433-3p by hnRNPA2B1 into the intestinal sEV to increase the abundance of miR-433-3p. DIEs delivered miR-433-3p to lipopolysaccharide-induced macrophages and targeted the MAPK8 gene, leading to inhibition of the MAPK signaling pathway and reduced production of inflammatory cytokines. One protective mechanism of DOP is mediated by intestinal sEV containing miR-433-3p, which is a potential therapeutic agent for the prevention of inflammatory factor accumulation from excessive intestinal macrophage activity and for restoring homeostasis in the intestinal microenvironment.
多糖(DOP)可减轻炎症性肠病(IBD),但其在调节肠道上皮细胞(IEC)和巨噬细胞之间针对 IBD 的串扰中的作用尚不清楚。本研究旨在通过微小 RNA 在小细胞外囊泡(sEV)中的调节来研究 DOP 对肠道炎症反应的保护作用。我们的结果表明,DOP 干扰了 IEC 分泌的小细胞外囊泡(DIEs),从而降低了炎症介质的水平。DIEs 中 miR-433-3p 的表达增加被认为是对抗肠道炎症的重要保护因子。DOP 通过 hnRNPA2B1 调节 miR-433-3p 加载到肠道 sEV 中,从而增加 miR-433-3p 的丰度。DIEs 将 miR-433-3p 递送至脂多糖诱导的巨噬细胞,并靶向 MAPK8 基因,从而抑制 MAPK 信号通路并减少炎症细胞因子的产生。DOP 的一种保护机制是通过含有 miR-433-3p 的肠道 sEV 介导的,这是一种预防过度肠道巨噬细胞活性引起的炎症因子积累和恢复肠道微环境平衡的潜在治疗剂。