结肠炎
炎症性肠病
巨噬细胞极化
微生物学
分泌物
巨噬细胞
MAPK/ERK通路
短链脂肪酸
体外
乳酸菌
生物
信号转导
生物化学
化学
免疫学
丁酸盐
医学
内科学
疾病
发酵
作者
Zhifeng Wu,Jinhui He,Zeyue Zhang,Jingjing Li,Huicong Zou,Xiang Tan,Yuqing Wang,Yong Yao,Wen Xiong
标识
DOI:10.1021/acs.jafc.3c00278
摘要
In this study, we investigated the effects of Lactobacillus johnsonii on the mouse colitis model. The results showed that the supernatant of the L. johnsonii culture alleviated colitis and remodeled gut microbiota, represented by an increased abundance of bacteria producing short-chain fatty acids, leading to an increased concentration of propionic acid in the intestine. Further studies revealed that propionic acid inhibited activation of the MAPK signaling pathway and polarization of M1 macrophages. Macrophage clearance assays confirmed that macrophages are indispensable for alleviating colitis through propionic acid. In vitro experiments showed that propionic acid directly inhibited the MAPK signaling pathway in macrophages and reduced M1 macrophage polarization, thereby inhibiting the secretion of pro-inflammatory cytokines. These findings improve our understanding of how L. johnsonii attenuates inflammatory bowel disease (IBD) and provide valuable insights for identifying molecular targets for IBD treatment in the future.
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