类有机物
益生元
丁酸盐
粘蛋白
功能(生物学)
消化(炼金术)
发酵
微生物学
肠道菌群
新陈代谢
势垒函数
生物
化学
粘蛋白2
肠粘膜
粪便
LGR5型
干细胞
肠上皮
细胞生物学
小肠
微生物代谢
细菌生长
上皮
碳酸钙-2
胃肠道
生物活性
平衡
生物化学
作者
Hanluo Li,Linda Liu,Jiaxin Liu,Hang Zheng,Jing Long,Jingyi Wang,Seockmo Ku,Meilin Weng,Sini Kang
标识
DOI:10.1021/acs.jafc.5c09432
摘要
Butyryl-fructooligosaccharides (B-FOSs) are prebiotic derivatives synthesized by ester-linked conjugation of fructooligosaccharides (FOSs) with butyrate, exhibiting enhanced prebiotic capabilities over conventional FOSs. However, their therapeutic mechanisms remain incompletely characterized. Our in vitro analyses revealed that B-FOSs resist gastrointestinal digestion and undergo fecal microbial fermentation, indicating their capacity to deliver butyrate to the colon. By integrating in vitro fecal fermentation with 3D colonoids derived from Lgr5+ intestinal stem cells, we systematically explored B-FOS-mediated microbiota–metabolite interactions. Organoid proliferation and viability were enhanced by B-FOS metabolites and a reshaped gut microbiota, which also counteracted liposaccharide (LPS)-induced epithelial disruption by upregulating ZO-1 and MUC2 expression. Notably, B-FOS-fermented supernatants demonstrated superior barrier-protective efficacy than was achieved using equivalent doses of butyrate, suggesting effects of other microbiota-derived metabolites. The B-FOS-modulated microbiota outperformed bacterial controls in terms of MUC2 and ZO-1 production, with Weissella identified as a critical degrader driving B-FOS metabolism and mucin biosynthesis.
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