Abteilung Mikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Barbarastr. 11, 49076 Osnabrück, Germany.
Nanoscale. 2013 Oct 7;5(19):9296-309. doi: 10.1039/c3nr01550e. Epub 2013 Aug 14.
The study of pathogen interactions with eukaryotic host cells requires the introduction of fluorescent probes to visualize processes such as endocytosis, intracellular transport or host cell manipulation by the pathogen. Here, three types of fluorescent nanoparticles (NPs), i.e. Rhodamine-labeled polymethacrylate (PMA) NPs, silica NPs and gold NPs, were employed to label the host cellular endolysosomal system and monitor manipulations by the pathogen Salmonella enterica. Using live cell imaging, we investigated the performance of NPs in cellular uptake, labeling of endocytic vesicles and lysosomes, as well as interaction with the pathogen. We show that fluorescent gold and silica, but not PMA NPs appropriately label host cell structures and efficiently track rearrangements of the host endosomal system by the activities of intracellular Salmonella. Silica NPs slightly aggregated and located in Salmonella-induced compartments as isolated dots, while gold NPs distributed uniformly inside such structures. Both silica and gold NPs exhibited no adverse impact on either host cells or pathogens, and are versatile tools for infection biology.
该研究通过引入荧光探针来可视化真核宿主细胞与病原体的相互作用过程,如内吞作用、细胞内运输或病原体对宿主细胞的操纵。在此,我们使用了三种类型的荧光纳米颗粒(NPs),即罗丹明标记的聚甲基丙烯酸酯(PMA)NPs、硅纳米颗粒和金纳米颗粒,标记宿主细胞的内吞体系统,并监测病原体沙门氏菌的操纵。通过活细胞成像,我们研究了 NPs 在细胞摄取、内吞小泡和溶酶体标记以及与病原体相互作用方面的性能。我们发现,荧光金纳米颗粒和硅纳米颗粒而非 PMA NPs 可以适当标记宿主细胞结构,并有效地跟踪细胞内沙门氏菌活性引起的宿主内吞体系统的重排。硅纳米颗粒略微聚集并位于沙门氏菌诱导的隔室中,呈孤立点,而金纳米颗粒均匀分布在这些结构内。硅纳米颗粒和金纳米颗粒均未对宿主细胞或病原体产生不良影响,是感染生物学的通用工具。