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有读书笔记Crohn's disease adherent-invasive Escherichia coli colonize and induce strong gut inflammation in transgenic mice expressing human CEACAM

聚焦生物 添加于 2009-11-30 01:21 | 953 次阅读 | 0 个评论
  •  作 者

    Carvalho FA, Barnich N, Sivignon A, Darcha C, Chan CHF, Stanners CP, Darfeuille-Michaud A
  •  摘 要

    Abnormal expression of CEACAM6 is observed at the apical surface of the ileal epithelium in Crohn's disease (CD) patients, and CD ileal lesions are colonized by pathogenic adherent-invasive Escherichia coli (AIEC). We investigated the ability of AIEC reference strain LF82 to colonize the intestinal mucosa and to induce inflammation in CEABAC10 transgenic mice expressing human CEACAMs. AIEC LF82 virulent bacteria, but not nonpathogenic E. coli K-12, were able to persist in the gut of CEABAC10 transgenic mice and to induce severe colitis with reduced survival rate, marked weight loss, increased rectal bleeding, presence of erosive lesions, mucosal inflammation, and increased proinflammatory cytokine expression. The colitis depended on type 1 pili expression by AIEC bacteria and on intestinal CEACAM expression because no sign of colitis was observed in transgenic mice infected with type 1 pili-negative LF82-Delta fimH isogenic mutant or in wild-type mice infected with AIEC LF82 bacteria. These findings strongly support the hypothesis that in CD patients having an abnormal intestinal expression of CEACAM6, AIEC bacteria via type 1 pili expression can colonize the intestinal mucosa and induce gut inflammation. Thus, targeting AIEC adhesion to gut mucosa represents a new strategy for clinicians to prevent and/or to treat ileal CD.
  •  详细资料

    • 关键词: Adhesins, Escherichia coli/physiology; Animals; Antigens, CD/*physiology; Bacterial Adhesion; Cell Adhesion Molecules/*physiology; Colitis/*etiology; Crohn Disease/*microbiology; Escherichia coli/*pathogenicity; Fimbriae Proteins/physiology; Gastrointestinal Tract/*microbiology; Humans; Mice; Mice, Transgenic
    • 文献种类:期刊
    • 期刊名称: The Journal of Experimental Medicine
    • 期刊缩写: J Exp Med
    • 期卷页: 2009  206 10 2179-2189
    • 地址: Universite Clermont 1, Pathogenie Bacterienne Intestinale, JE2526, Unite Sous Contrat Institut National de la Recherche Agronomique 2018, Clermont-Ferrand F-63001, France
    • ISBN: 1540-9538
    • 备注:PMID:19737864
  • 相关链接 DOI URL 

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    发现克罗恩氏病的关键分子机制


    法国国家农艺研究所11月25日发表公报说,他们与美国克莱蒙大学的研究人员通过共同研究发现,肠细胞中一种分子的异常表达会导致人患上克罗恩氏病,这一成果将有助于开发防治这种疾病的新方法。
     
    据该研究所介绍,克罗恩氏病,即节段性回肠炎,是一种在欧美比较常见的肠道疾病,目前欧 洲和美国分别约有75万名和55万名患者。它会引起消化系统发炎,具体症状包括腹痛、腹泻、直肠出血、体重减轻和关节炎等。这种病往往难于确诊,因为它的 症状与肠过敏和溃疡性结肠炎等其他肠道疾病相似。
     
    此前不少研究人员认为,克罗恩氏病是由一种传染性病菌引起的。由阿莱特·达尔弗耶-米肖领导的研究小组从1998年就开始研究,他们发现,一种名为CEACAM6的分子的异常表达会促使大肠杆菌附着在肠道的上皮细胞上,并且不断繁殖,从而引发消化系统发炎。
     
    为验证这一结果,科学家对克罗恩氏病患者和正常人进行了比较。结果发现,CEACAM6分子在35%的病人回肠里出现表达异常,而在正常人体内则处于“沉默”状态。
     
    研究小组表示,未来可以通过阻断CEACAM6分子与大肠杆菌的相互作用,达到预防克罗恩氏病的目的。

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