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抗菌肽在先天性宿主防御中的作用。

The roles of antimicrobial peptides in innate host defense.

作者信息

Diamond Gill, Beckloff Nicholas, Weinberg Aaron, Kisich Kevin O

机构信息

Department of Oral Biology, UMDNJ-New Jersey Dental School, Newark, NJ 07101, USA.

出版信息

Curr Pharm Des. 2009;15(21):2377-92. doi: 10.2174/138161209788682325.

DOI:10.2174/138161209788682325
PMID:19601838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2750833/
Abstract

Antimicrobial peptides (AMPs) are multi-functional peptides whose fundamental biological role in vivo has been proposed to be the elimination of pathogenic microorganisms, including Gram-positive and -negative bacteria, fungi, and viruses. Genes encoding these peptides are expressed in a variety of cells in the host, including circulating phagocytic cells and mucosal epithelial cells, demonstrating a wide range of utility in the innate immune system. Expression of these genes is tightly regulated; they are induced by pathogens and cytokines as part of the host defense response, and they can be suppressed by bacterial virulence factors and environmental factors which can lead to increased susceptibility to infection. New research has also cast light on alternative functionalities, including immunomodulatory activities, which are related to their unique structural characteristics. These peptides represent not only an important component of innate host defense against microbial colonization and a link between innate and adaptive immunity, but also form a foundation for the development of new therapeutic agents.

摘要

抗菌肽(AMPs)是多功能肽,其在体内的基本生物学作用被认为是清除致病微生物,包括革兰氏阳性和阴性细菌、真菌及病毒。编码这些肽的基因在宿主的多种细胞中表达,包括循环吞噬细胞和黏膜上皮细胞,这表明它们在先天免疫系统中具有广泛用途。这些基因的表达受到严格调控;它们作为宿主防御反应的一部分,由病原体和细胞因子诱导表达,并且可被细菌毒力因子和环境因子抑制,这些因子会导致感染易感性增加。新的研究还揭示了抗菌肽的其他功能,包括免疫调节活性,这与其独特的结构特征有关。这些肽不仅是宿主抵御微生物定植的先天防御的重要组成部分,也是先天免疫与适应性免疫之间的联系,而且还为新型治疗药物的开发奠定了基础。

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本文引用的文献

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Antimicrobial peptide mimics for improved therapeutic properties.具有改善治疗特性的抗菌肽模拟物。
Biochim Biophys Acta. 2009 Aug;1788(8):1582-92. doi: 10.1016/j.bbamem.2008.10.020. Epub 2008 Nov 5.
2
De novo designed synthetic mimics of antimicrobial peptides.抗菌肽的从头设计合成模拟物。
Curr Opin Biotechnol. 2008 Dec;19(6):620-7. doi: 10.1016/j.copbio.2008.10.013. Epub 2008 Nov 17.
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Host defense peptides in the oral cavity and the lung: similarities and differences.口腔和肺部的宿主防御肽:异同
J Dent Res. 2008 Oct;87(10):915-27. doi: 10.1177/154405910808701011.
4
Antimicrobial peptides, skin infections, and atopic dermatitis.抗菌肽、皮肤感染与特应性皮炎
Semin Cutan Med Surg. 2008 Jun;27(2):144-50. doi: 10.1016/j.sder.2008.04.002.
5
Defective killing of Staphylococcus aureus in atopic dermatitis is associated with reduced mobilization of human beta-defensin-3.特应性皮炎中金黄色葡萄球菌杀伤缺陷与人类β-防御素-3的动员减少有关。
J Allergy Clin Immunol. 2008 Jul;122(1):62-8. doi: 10.1016/j.jaci.2008.04.022. Epub 2008 Jun 5.
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Computational analysis suggests beta-defensins are processed to mature peptides by signal peptidase.计算分析表明,β-防御素由信号肽加工成成熟肽。
Protein Pept Lett. 2008;15(5):536-40. doi: 10.2174/092986608784567618.
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IL-12, IL-23, and IL-27 enhance human beta-defensin-2 production in human keratinocytes.白细胞介素-12、白细胞介素-23和白细胞介素-27可增强人角质形成细胞中人β-防御素-2的产生。
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