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本文引用的文献

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Degradation of human alpha- and beta-defensins by culture supernatants of Porphyromonas gingivalis strain 381.牙龈卟啉单胞菌 381 株培养上清液对人α-和β-防御素的降解作用。
J Innate Immun. 2009;1(2):118-22. doi: 10.1159/000181015. Epub 2008 Dec 2.
2
High molecular weight gingipains from Porphyromonas gingivalis induce cytokine responses from human macrophage-like cells via a nonproteolytic mechanism.牙龈卟啉单胞菌高分子量gingipains 通过非蛋白水解机制诱导人巨噬样细胞的细胞因子反应。
J Innate Immun. 2009;1(2):109-17. doi: 10.1159/000181145. Epub 2008 Dec 2.
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A new pathway of staphylococcal pathogenesis: apoptosis-like death induced by Staphopain B in human neutrophils and monocytes.葡萄球菌致病新途径:葡萄球菌蛋白酶 B 在人中性粒细胞和单核细胞中诱导的细胞凋亡样死亡。
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Activation of TAFI on the surface of Streptococcus pyogenes evokes inflammatory reactions by modulating the kallikrein/kinin system.化脓链球菌表面 TAFI 的激活通过调节激肽释放酶/激肽系统引发炎症反应。
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The role of epithelial integrin receptors in recognition of pulmonary pathogens.上皮细胞整合素受体在识别肺部病原体中的作用。
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Proteinases as hormones: targets and mechanisms for proteolytic signaling.作为激素的蛋白酶:蛋白水解信号传导的靶点与机制
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Binding of complement inhibitor C4b-binding protein contributes to serum resistance of Porphyromonas gingivalis.补体抑制剂C4b结合蛋白的结合有助于牙龈卟啉单胞菌的血清抗性。
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The human protease inhibitor cystatin C is an activating cofactor for the streptococcal cysteine protease IdeS.人蛋白酶抑制剂胱抑素C是链球菌半胱氨酸蛋白酶IdeS的激活辅因子。
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Mechanism of methaemoglobin breakdown by the lysine-specific gingipain of the periodontal pathogen Porphyromonas gingivalis.牙周病原体牙龈卟啉单胞菌的赖氨酸特异性牙龈蛋白酶对高铁血红蛋白的分解机制。
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细菌蛋白酶对固有免疫的影响。

Corruption of innate immunity by bacterial proteases.

机构信息

Department of Microbiology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.

出版信息

J Innate Immun. 2009;1(2):70-87. doi: 10.1159/000181144.

DOI:10.1159/000181144
PMID:19756242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2743019/
Abstract

The innate immune system of the human body has developed numerous mechanisms to control endogenous and exogenous bacteria and thus prevent infections by these microorganisms. These mechanisms range from physical barriers such as the skin or mucosal epithelium to a sophisticated array of molecules and cells that function to suppress or prevent bacterial infection. Many bacteria express a variety of proteases, ranging from non-specific and powerful enzymes that degrade many proteins involved in innate immunity to proteases that are extremely precise and specific in their mode of action. Here we have assembled a comprehensive picture of how bacterial proteases affect the host's innate immune system to gain advantage and cause infection. This picture is far from being complete since the numbers of mechanisms utilized are as astonishing as they are diverse, ranging from degradation of molecules vital to innate immune mechanisms to subversion of the mechanisms to allow the bacterium to hide from the system or take advantage of it. It is vital that such mechanisms are elucidated to allow strategies to be developed to aid the innate immune system in controlling bacterial infections.

摘要

人体的先天免疫系统已经发展出许多机制来控制内源性和外源性细菌,从而预防这些微生物的感染。这些机制包括从皮肤或粘膜上皮等物理屏障到一系列复杂的分子和细胞,它们的功能是抑制或预防细菌感染。许多细菌表达各种蛋白酶,范围从非特异性和强大的酶,这些酶可以降解许多参与先天免疫的蛋白质,到作用模式极其精确和特异的蛋白酶。在这里,我们综合描述了细菌蛋白酶如何影响宿主的先天免疫系统以获得优势并引起感染。由于所利用的机制数量之多令人惊讶,而且种类繁多,从降解对先天免疫机制至关重要的分子到颠覆这些机制以使细菌能够躲避或利用该系统,这幅画面远非完整。阐明这些机制对于制定策略来帮助先天免疫系统控制细菌感染至关重要。