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锌与固有免疫的一种合金:增强宿主抗感染防御能力。

An alloy of zinc and innate immunity: Galvanising host defence against infection.

作者信息

von Pein Jessica B, Stocks Claudia J, Schembri Mark A, Kapetanovic Ronan, Sweet Matthew J

机构信息

Institute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Queensland, Australia.

IMB Centre for Inflammation and Disease Research, The University of Queensland, St. Lucia, Queensland, Australia.

出版信息

Cell Microbiol. 2021 Jan;23(1):e13268. doi: 10.1111/cmi.13268. Epub 2020 Oct 9.

Abstract

Innate immune cells such as macrophages and neutrophils initiate protective inflammatory responses and engage antimicrobial responses to provide frontline defence against invading pathogens. These cells can both restrict the availability of certain transition metals that are essential for microbial growth and direct toxic concentrations of metals towards pathogens as antimicrobial responses. Zinc is important for the structure and function of many proteins, however excess zinc can be cytotoxic. In recent years, several studies have revealed that innate immune cells can deliver toxic concentrations of zinc to intracellular pathogens. In this review, we discuss the importance of zinc status during infectious disease and the evidence for zinc intoxication as an innate immune antimicrobial response. Evidence for pathogen subversion of this response is also examined. The likely mechanisms, including the involvement of specific zinc transporters that facilitate delivery of zinc by innate immune cells for metal ion poisoning of pathogens are also considered. Precise mechanisms by which excess levels of zinc can be toxic to microorganisms are then discussed, particularly in the context of synergy with other antimicrobial responses. Finally, we highlight key unanswered questions in this emerging field, which may offer new opportunities for exploiting innate immune responses for anti-infective development.

摘要

巨噬细胞和中性粒细胞等先天免疫细胞启动保护性炎症反应并参与抗菌反应,以提供针对入侵病原体的一线防御。这些细胞既能限制微生物生长所必需的某些过渡金属的可用性,又能将金属的有毒浓度导向病原体,作为抗菌反应。锌对许多蛋白质的结构和功能很重要,然而过量的锌可能具有细胞毒性。近年来,多项研究表明,先天免疫细胞可以将有毒浓度的锌传递给细胞内病原体。在这篇综述中,我们讨论了传染病期间锌状态的重要性以及锌中毒作为一种先天免疫抗菌反应的证据。还研究了病原体颠覆这种反应的证据。还考虑了可能的机制,包括特定锌转运体的参与,这些转运体促进先天免疫细胞输送锌,以对病原体进行金属离子中毒。然后讨论了过量锌对微生物有毒的精确机制,特别是在与其他抗菌反应协同作用的背景下。最后,我们强调了这个新兴领域中尚未解决的关键问题,这可能为利用先天免疫反应进行抗感染开发提供新的机会。

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