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真菌病原体对宿主吞噬作用的调控及治疗机会

Manipulation of host phagocytosis by fungal pathogens and therapeutic opportunities.

机构信息

Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, Germany.

Junior Research Group Phagosome Biology and Engineering, Leibniz-HKI, Jena, Germany.

出版信息

Nat Microbiol. 2024 Sep;9(9):2216-2231. doi: 10.1038/s41564-024-01780-0. Epub 2024 Aug 26.

DOI:10.1038/s41564-024-01780-0
PMID:39187614
Abstract

An important host defence mechanism against pathogens is intracellular killing, which is achieved through phagocytosis, a cellular process for engulfing and neutralizing extracellular particles. Phagocytosis results in the formation of matured phagolysosomes, which are specialized compartments that provide a hostile environment and are considered the end point of the degradative pathway. However, all fungal pathogens studied to date have developed strategies to manipulate phagosomal function directly and also indirectly by redirecting phagosomes from the degradative pathway to a non-degradative pathway with the expulsion and even transfer of pathogens between cells. Here, using the major human fungal pathogens Aspergillus fumigatus, Candida albicans, Cryptococcus neoformans and Histoplasma capsulatum as examples, we discuss the processes involved in host phagosome-fungal pathogen interactions, with a focus on fungal evasion strategies. We also discuss recent approaches to targeting intraphagosomal pathogens, including the redirection of phagosomes towards degradative pathways for fungal pathogen eradication.

摘要

宿主防御机制的一个重要方面是细胞内杀伤,这是通过吞噬作用实现的,吞噬作用是一种吞噬和中和细胞外颗粒的细胞过程。吞噬作用导致成熟的吞噬体的形成,吞噬体是专门的隔室,提供了恶劣的环境,并被认为是降解途径的终点。然而,迄今为止研究的所有真菌病原体都已经开发出了直接操纵吞噬体功能的策略,并且还通过将吞噬体从降解途径重新定向到非降解途径来间接操纵吞噬体功能,从而将病原体排出甚至在细胞之间转移。在这里,我们使用主要的人类真菌病原体烟曲霉、白念珠菌、新生隐球菌和荚膜组织胞浆菌作为例子,讨论宿主吞噬体-真菌病原体相互作用中涉及的过程,重点是真菌逃避策略。我们还讨论了针对细胞内病原体的最新方法,包括将吞噬体重新定向到降解途径以根除真菌病原体。

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Nature. 2024 Jun;630(8017):736-743. doi: 10.1038/s41586-024-07499-6. Epub 2024 Jun 5.
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BTK drives neutrophil activation for sterilizing antifungal immunity.布鲁顿酪氨酸激酶(BTK)驱动中性粒细胞活化以实现抗真菌免疫清除。
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RAB5c controls the assembly of non-canonical autophagy machinery to promote phagosome maturation and microbicidal function of macrophages.RAB5c控制非经典自噬机制的组装,以促进巨噬细胞的吞噬体成熟和杀菌功能。
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Forward genetic screen in zebrafish identifies new fungal regulators that limit host-protective -innate immune interaction.斑马鱼中的正向遗传筛选鉴定出限制宿主保护性先天免疫相互作用的新型真菌调节因子。
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bioRxiv. 2025 Feb 15:2025.02.14.638315. doi: 10.1101/2025.02.14.638315.
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