| Literature DB >> 34818535 |
Cherng-Shyang Chang1, Yi-Chu Liao2, Chih-Ting Huang1, Chiao-Mei Lin1, Chantal Hoi Yin Cheung3, Jhen-Wei Ruan4, Wen-Hsuan Yu5, Yi-Ting Tsai1, I-Jung Lin1, Chien-Hsun Huang6, Jong-Shian Liou6, Ya-Hsien Chou7, Hung-Jen Chien7, Hsiao-Li Chuang8, Hsueh-Fen Juan9, Hsuan-Cheng Huang10, Hong-Lin Chan11, Yu-Chieh Liao2, Shiue-Cheng Tang12, Yu-Wen Su1, Tse-Hua Tan1, Andreas J Bäumler13, Cheng-Yuan Kao14.
Abstract
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.Entities:
Keywords: DUSP6; barrier integrity; experimental colitis; gut microbiota; leaky gut
Mesh:
Substances:
Year: 2021 PMID: 34818535 DOI: 10.1016/j.celrep.2021.110016
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423