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二价金属摄取及ZIP8在宿主抵御病原体中的作用

Divalent Metal Uptake and the Role of ZIP8 in Host Defense Against Pathogens.

作者信息

Samuelson Derrick R, Haq Sabah, Knoell Daren L

机构信息

Division of Pulmonary, Critical Care, and Sleep, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, United States.

Department of Pharmacy Practice and Science, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, United States.

出版信息

Front Cell Dev Biol. 2022 Jun 27;10:924820. doi: 10.3389/fcell.2022.924820. eCollection 2022.

Abstract

Manganese (Mn) and Zinc (Zn) are essential micronutrients whose concentration and location within cells are tightly regulated at the onset of infection. Two families of Zn transporters (ZIPs and ZnTs) are largely responsible for regulation of cytosolic Zn levels and to a certain extent, Mn levels, although much less is known regarding Mn. The capacity of pathogens to persevere also depends on access to micronutrients, yet a fundamental gap in knowledge remains regarding the importance of metal exchange at the host interface, often referred to as nutritional immunity. ZIP8, one of 14 ZIPs, is a pivotal importer of both Zn and Mn, yet much remains to be known. Dietary Zn deficiency is common and commonly occurring polymorphic variants of ZIP8 that decrease cellular metal uptake (Zn and Mn), are associated with increased susceptibility to infection. Strikingly, ZIP8 is the only Zn transporter that is highly induced following bacterial exposure in key immune cells involved with host defense against leading pathogens. We postulate that mobilization of Zn and Mn into key cells orchestrates the innate immune response through regulation of fundamental defense mechanisms that include phagocytosis, signal transduction, and production of soluble host defense factors including cytokines and chemokines. New evidence also suggests that host metal uptake may have long-term consequences by influencing the adaptive immune response. Given that activation of ZIP8 expression by pathogens has been shown to influence parenchymal, myeloid, and lymphoid cells, the impact applies to all mucosal surfaces and tissue compartments that are vulnerable to infection. We also predict that perturbations in metal homeostasis, either genetic- or dietary-induced, has the potential to impact bacterial communities in the host thereby adversely impacting microbiome composition. This review will focus on Zn and Mn transport ZIP8, and how this vital metal transporter serves as a "go to" conductor of metal uptake that bolsters host defense against pathogens. We will also leverage past studies to underscore areas for future research to better understand the Zn-, Mn- and ZIP8-dependent host response to infection to foster new micronutrient-based intervention strategies to improve our ability to prevent or treat commonly occurring infectious disease.

摘要

锰(Mn)和锌(Zn)是必需的微量营养素,在感染发生时,它们在细胞内的浓度和定位受到严格调控。锌转运蛋白的两个家族(ZIPs和ZnTs)在很大程度上负责调节细胞溶质锌水平,在一定程度上也负责调节锰水平,尽管关于锰的了解要少得多。病原体的生存能力也取决于对微量营养素的获取,然而,关于宿主界面处金属交换的重要性,即通常所说的营养免疫,在知识上仍存在一个基本空白。ZIP8是14种ZIPs之一,是锌和锰的关键导入蛋白,但仍有许多有待了解之处。饮食中锌缺乏很常见,而ZIP8常见的多态性变体可降低细胞对金属(锌和锰)的摄取,与感染易感性增加有关。引人注目的是,ZIP8是唯一一种在参与宿主抵御主要病原体的关键免疫细胞中细菌暴露后被高度诱导的锌转运蛋白。我们推测,锌和锰向关键细胞的动员通过调节包括吞噬作用、信号转导以及包括细胞因子和趋化因子在内的可溶性宿主防御因子的产生等基本防御机制来协调先天免疫反应。新证据还表明,宿主对金属的摄取可能通过影响适应性免疫反应而产生长期后果。鉴于病原体对ZIP8表达的激活已被证明会影响实质细胞、髓样细胞和淋巴细胞,这种影响适用于所有易受感染的粘膜表面和组织隔室。我们还预测,无论是遗传诱导还是饮食诱导的金属稳态扰动,都有可能影响宿主中的细菌群落,从而对微生物群组成产生不利影响。本综述将聚焦于锌和锰的转运、ZIP8,以及这种重要的金属转运蛋白如何作为增强宿主抵御病原体能力的金属摄取“指挥者”。我们还将利用过去的研究来强调未来研究的领域,以更好地理解锌、锰和ZIP8依赖的宿主对感染的反应,从而促进新的基于微量营养素的干预策略,以提高我们预防或治疗常见传染病的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04f0/9273032/16aeae17077b/fcell-10-924820-g001.jpg

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