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dc.contributor.author | Toyonaga, Takahiko | en |
dc.contributor.author | Nakase, Hiroshi | en |
dc.contributor.author | Ueno, Satoru | en |
dc.contributor.author | Matsuura, Minoru | en |
dc.contributor.author | Yoshino, Takuya | en |
dc.contributor.author | Honzawa, Yusuke | en |
dc.contributor.author | Itou, Ayako | en |
dc.contributor.author | Namba, Kazuyoshi | en |
dc.contributor.author | Minami, Naoki | en |
dc.contributor.author | Yamada, Satoshi | en |
dc.contributor.author | Koshikawa, Yorimitsu | en |
dc.contributor.author | Uede, Toshimitsu | en |
dc.contributor.author | Chiba, Tsutomu | en |
dc.contributor.author | Okazaki, Kazuichi | en |
dc.contributor.alternative | 豊永, 貴彦 | ja |
dc.contributor.alternative | 仲瀬, 裕志 | ja |
dc.date.accessioned | 2015-12-15T01:39:09Z | - |
dc.date.available | 2015-12-15T01:39:09Z | - |
dc.date.issued | 2015-08-14 | - |
dc.identifier.issn | 1932-6203 | - |
dc.identifier.uri | http://hdl.handle.net/2433/202591 | - |
dc.description.abstract | [Background]Osteopontin (OPN) is a multifunctional protein expressed in a variety of tissues and cells. Recent studies revealed increased OPN expression in the inflamed intestinal tissues of patients with inflammatory bowel disease (IBD). The role of OPN in the pathophysiology of IBD, however, remains unclear. [Aims]To investigate the role of OPN in the development of intestinal inflammation using a murine model of IBD, interleukin-10 knock out (IL-10 KO) mice. [Methods]We compared the development of colitis between IL-10 KO and OPN/IL-10 double KO (DKO) mice. OPN expression in the colonic tissues of IL-10 KO mice was examined by fluorescence in situ hybridization (FISH) analysis. Enteric microbiota were compared between IL-10 KO and OPN/IL-10 DKO mice by terminal restriction fragment length polymorphism analysis. The effect of OPN on macrophage phagocytic function was evaluated by phagocytosis assay. [Results]OPN/IL-10 DKO mice had an accelerated onset of colitis compared to IL-10 KO mice. FISH analysis revealed enhanced OPN synthesis in the colonic epithelial cells of IL-10 KO mice. OPN/IL-10 DKO mice had a distinctly different enteric bacterial profile with a significantly lower abundance of Clostridium subcluster XIVa and a greater abundance of Clostridium cluster XVIII compared to IL-10 KO mice. Intracellular OPN deletion in macrophages impaired phagocytosis of fluorescence particle-conjugated Escherichia coli in vitro. Exogenous OPN enhanced phagocytosis by OPN-deleted macrophages when administered at doses of 1 to 100 ng/ml, but not 1000 ng/ml. [Conclusions]OPN deficiency accelerated the spontaneous development of colitis in mice with disrupted gut microbiota and macrophage phagocytic activity. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Public Library of Science | en |
dc.rights | © 2015 Toyonaga et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | en |
dc.title | Osteopontin Deficiency Accelerates Spontaneous Colitis in Mice with Disrupted Gut Microbiota and Macrophage Phagocytic Activity. | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | PLOS ONE | en |
dc.identifier.volume | 10 | - |
dc.identifier.issue | 8 | - |
dc.relation.doi | 10.1371/journal.pone.0135552 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | e0135552 | - |
dc.identifier.pmid | 26274807 | - |
dcterms.accessRights | open access | - |
出現コレクション: | 学術雑誌掲載論文等 |
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