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Human a-Defensin 6 Promotes Mucosal Innate Immunity Through Self-Assembled Peptide Nanonets

机译:人类α-防御素6通过自组装肽纳米网促进粘膜固有免疫。

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摘要

Defensins are antimicrobial peptides that contribute broadly to innate immunity, including protection of mucosal tissues. Human α-defensin (HD) 6 is highly expressed by secretory Paneth cells of the small intestine. However, in contrast to the other defensins, it lacks appreciable bactericidal activity. Nevertheless, we report here that HD6 affords protection against invasion by enteric bacterial pathogens in vitro and in vivo. After stochastic binding to bacterial surface proteins, HD6 undergoes ordered self-assembly to form fibrils and nanonets that surround and entangle bacteria. This self-assembly mechanism occurs in vivo, requires histidine-27, and is consistent with x-ray crystallography data. These findings support a key role for HD6 in protecting the small intestine against invasion by diverse enteric pathogens and may explain the conservation of HD6 throughout Hominidae evolution.
机译:防御素是抗菌肽,可广泛促进先天免疫,包括保护粘膜组织。人α-防御素(HD)6在小肠的分泌性Paneth细胞中高度表达。但是,与其他防御素相比,它缺乏明显的杀菌活性。尽管如此,我们在这里报道HD6可以在体外和体内提供针对肠道细菌病原体入侵的保护作用。与细菌表面蛋白随机结合后,HD6经历有序的自组装,形成围绕并缠结细菌的原纤维和纳米网。这种自组装机制在体内发生,需要组氨酸27,并且与X射线晶体学数据一致。这些发现支持HD6在保护小肠免受各种肠道病原体侵袭中的关键作用,并可能解释了在整个人科进化过程中HD6的保守性。

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  • 来源
    《Science》 |2012年第6093期|p.477-481|共5页
  • 作者单位

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Institute of Human Virology and Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA;

    Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, 70376 Stuttgart, Germany;

    Department of Gastroenterology and Hepatology, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA;

    Department of Pediatrics, Division of Gastroenterology, Medical College of Wisconsin, Milwaukee, WI 53226, USA;

    Department of Pediatrics, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Food Science and Technology, University of California, Davis, CA 95616, USA;

    Institute of Human Virology and Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA;

    Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

    Department of Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616, USA;

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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:53:32

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