肠道菌群
失调
基因剔除小鼠
结肠炎
生物
免疫学
生物化学
基因
作者
Cherng–Shyang Chang,Yi-Chu Liao,Chih‐Ting Huang,Chiao-Mei Lin,Chantal Hoi Yin Cheung,Jhen‐Wei Ruan,Wen-Hsuan Yu,Yi‐Ting Tsai,I-Jung Lin,Chien‐Hsun Huang,Jong-Shian Liou,Ya-Hsien Chou,Hung‐Jen Chien,Hsiao-Li Chuang,Hsueh‐Fen Juan,Y. Hoshi,Hong‐Lin Chan,Yu-Chieh Liao,Shiue–Cheng Tang,Yu‐Wen Su,Tse‐Hua Tan,Andreas J. Bäumler,Cheng‐Yuan Kao
出处
期刊:Cell Reports
[Elsevier]
日期:2021-11-01
卷期号:37 (8): 110016-110016
被引量:46
标识
DOI:10.1016/j.celrep.2021.110016
摘要
Strengthening the gut epithelial barrier is a potential strategy for management of gut microbiota-associated illnesses. Here, we demonstrate that dual-specificity phosphatase 6 (Dusp6) knockout enhances baseline colon barrier integrity and ameliorates dextran sulfate sodium (DSS)-induced colonic injury. DUSP6 mutation in Caco-2 cells enhances the epithelial feature and increases mitochondrial oxygen consumption, accompanied by altered glucose metabolism and decreased glycolysis. We find that Dusp6-knockout mice are more resistant to DSS-induced dysbiosis, and the cohousing and fecal microbiota transplantation experiments show that the gut/fecal microbiota derived from Dusp6-knockout mice also confers protection against colitis. Further culturomics and mono-colonialization experiments show that one gut microbiota member in the genus Duncaniella confers host protection from DSS-induced injury. We identify Dusp6 deficiency as beneficial for shaping the gut microbiota eubiosis necessary to protect against gut barrier-related diseases.
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