| Literature DB >> 27027293 |
Ryu Okumura1,2, Takashi Kurakawa1, Takashi Nakano3, Hisako Kayama1,2, Makoto Kinoshita1,2, Daisuke Motooka4, Kazuyoshi Gotoh4,5, Taishi Kimura1, Naganori Kamiyama1, Takashi Kusu1, Yoshiyasu Ueda1, Hong Wu3, Hideki Iijima6, Soumik Barman1,2, Hideki Osawa7, Hiroshi Matsuno7, Junichi Nishimura7, Yusuke Ohba8, Shota Nakamura4, Tetsuya Iida4,9, Masahiro Yamamoto10, Eiji Umemoto1,2, Koichi Sano3, Kiyoshi Takeda1,2.
Abstract
Colonic epithelial cells are covered by thick inner and outer mucus layers. The inner mucus layer is free of commensal microbiota, which contributes to the maintenance of gut homeostasis. In the small intestine, molecules critical for prevention of bacterial invasion into epithelia such as Paneth-cell-derived anti-microbial peptides and regenerating islet-derived 3 (RegIII) family proteins have been identified. Although there are mucus layers providing physical barriers against the large number of microbiota present in the large intestine, the mechanisms that separate bacteria and colonic epithelia are not fully elucidated. Here we show that Ly6/PLAUR domain containing 8 (Lypd8) protein prevents flagellated microbiota invading the colonic epithelia in mice. Lypd8, selectively expressed in epithelial cells at the uppermost layer of the large intestinal gland, was secreted into the lumen and bound flagellated bacteria including Proteus mirabilis. In the absence of Lypd8, bacteria were present in the inner mucus layer and many flagellated bacteria invaded epithelia. Lypd8(-/-) mice were highly sensitive to intestinal inflammation induced by dextran sulfate sodium (DSS). Antibiotic elimination of Gram-negative flagellated bacteria restored the bacterial-free state of the inner mucus layer and ameliorated DSS-induced intestinal inflammation in Lypd8(-/-) mice. Lypd8 bound to flagella and suppressed motility of flagellated bacteria. Thus, Lypd8 mediates segregation of intestinal bacteria and epithelial cells in the colon to preserve intestinal homeostasis.Entities:
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Year: 2016 PMID: 27027293 DOI: 10.1038/nature17406
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962