LGR5型
坏死性小肠结肠炎
势垒函数
Wnt信号通路
鼠李糖乳杆菌
紧密连接
小肠结肠炎
肠道疾病
肿瘤坏死因子α
肠上皮
肠粘膜
癌症研究
生物
细胞生物学
信号转导
免疫学
医学
内科学
乳酸菌
病理
上皮
生物化学
疾病
发酵
作者
Yang Li,Junfei Chen,Dong Sun,Jingwei Liu,Zhe Wang,Aiwu Li
标识
DOI:10.1016/j.jff.2022.105243
摘要
Intestinal barrier function and intestinal flora imbalance lead to neonatal necrotizing enterocolitis (NEC). Lactobacillus rhamnosus GG (LGG) has been used to prevent or treat NEC in many animal models and clinical trials; however, its underlying action mechanism remains elucidated. Here, we observed intestinal stem cell (ISC) and intestinal barrier disruption in an NEC mouse model, characterized by reduced number of tight junctions (TJs) and expression of Lgr5, inhibition of ISC differentiation and the Wnt/β-catenin signaling pathway, and disturbance of the intestinal microbiota microenvironment. LGG oral administration in these mice re-established the intestinal flora, increased Wnt3a and Wnt7b levels in the small intestinal tissue, activated the Wnt/β-catenin signaling pathway, promoted ISC regeneration, reduced intestinal tumor necrosis factor-α and interleukin-6 levels, increased the number of TJs, and improved intestinal barrier function; NEC-induced intestinal injury was also reduced. Therefore, LGG administration can alleviate intestinal lesions by enhancing mucosal barrier function in NEC.
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