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Frizzled proteins are colonic epithelial receptors for C. difficile toxin B

机译:卷曲蛋白是艰难梭菌毒素B的结肠上皮受体

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摘要

Clostridium difficile toxin B (TcdB) is a critical virulence factor that causes diseases associated with C. difficile infection. Here we carried out CRISPR-Cas9-mediated genome-wide screens and identified the members of the Wnt receptor frizzled family (FZDs) as TcdB receptors. TcdB binds to the conserved Wnt-binding site known as the cysteine-rich domain (CRD), with the highest affinity towards FZD1, 2 and 7. TcdB competes with Wnt for binding to FZDs, and its binding blocks Wnt signalling. FZD1/2/7 triple-knockout cells are highly resistant to TcdB, and recombinant FZD2-CRD prevented TcdB binding to the colonic epithelium. Colonic organoids cultured from FZD7-knockout mice, combined with knockdown of FZD1 and 2, showed increased resistance to TcdB. The colonic epithelium in FZD7-knockout mice was less susceptible to TcdB-induced tissue damage in vivo. These findings establish FZDs as physiologically relevant receptors for TcdB in the colonic epithelium.
机译:艰难梭菌毒素B(TcdB)是导致与艰难梭菌感染有关的疾病的重要毒力因子。在这里,我们进行了CRISPR-Cas9介导的全基因组筛选,并将Wnt受体卷曲家族(FZDs)的成员鉴定为TcdB受体。 TcdB结合到保守的Wnt结合位点,即富含半胱氨酸的结构域(CRD),对FZD1、2和7具有最高的亲和力。TcdB与Wnt竞争与FZDs的结合,其结合阻断Wnt信号传导。 FZD1 / 2/7三重敲除细胞对TcdB具有高度抗性,重组FZD2-CRD阻止TcdB与结肠上皮结合。从FZD7敲除小鼠培养的结肠类器官与FZD1和2的敲低结合显示出对TcdB的抗性增加。 FZD7敲除小鼠中的结肠上皮细胞不易受TcdB诱导的体内组织损伤。这些发现将FZDs确定为结肠上皮中TcdB的生理相关受体。

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  • 来源
    《Nature》 |2016年第7625期|350-355|共6页
  • 作者单位

    Harvard Med Sch, Boston Childrens Hosp, Dept Urol, Boston, MA 02115 USA|Harvard Med Sch, Dept Microbiol & Immunobiol, Boston, MA 02115 USA|Harvard Med Sch, Dept Surg, Boston, MA 02115 USA;

    Harvard Med Sch, Boston Childrens Hosp, Dept Urol, Boston, MA 02115 USA|Harvard Med Sch, Dept Microbiol & Immunobiol, Boston, MA 02115 USA|Harvard Med Sch, Dept Surg, Boston, MA 02115 USA;

    Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst MaPS, Worcester, MA 01655 USA;

    Boston Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA;

    Texas A&M Hlth Sci Ctr, Ctr Infect & Inflammatory Dis, Houston, TX 77030 USA;

    Hannover Med Sch, Inst Toxicol, D-30625 Hannover, Germany;

    Harvard Med Sch, Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA|Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA;

    Sanford Burnham Prebys Med Discovery Inst, Tumor Microenvironm & Canc Immunol Program, La Jolla, CA 92037 USA;

    Boston Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA|Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA;

    Harvard Med Sch, Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA|Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA;

    Texas A&M Hlth Sci Ctr, Ctr Infect & Inflammatory Dis, Houston, TX 77030 USA;

    Boston Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA|Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA|Harvard Stem Cell Inst, Cambridge, MA 02138 USA;

    Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst MaPS, Worcester, MA 01655 USA|Univ Massachusetts, Sch Med, Dept Med, Gastroenterol Div, Worcester, MA 01655 USA;

    Harvard Med Sch, Boston Childrens Hosp, Dept Urol, Boston, MA 02115 USA|Harvard Med Sch, Dept Microbiol & Immunobiol, Boston, MA 02115 USA|Harvard Med Sch, Dept Surg, Boston, MA 02115 USA;

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  • 入库时间 2022-08-18 02:52:17

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