Lertjuthaporn Sakaorat, Somkird Jinjuta, Lekmanee Kittima, Atipimonpat Anyapat, Sukapirom Kasama, Sawasdipokin Hathai, Tiewcharoen Supathra, Pattanapanyasat Kovit, Khowawisetsut Ladawan
Center for Research and Innovation, Faculty of Medical Technology, Mahidol University, Nakhon Pathom 73170, Thailand.
Graduate Program in Anatomy, Department of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Pathogens. 2022 May 30;11(6):632. doi: 10.3390/pathogens11060632.
Extracellular vesicles (EVs) released from pathogenic protozoans play crucial roles in host-parasite communication and disease pathogenesis. is a free-living protozoan causing primary amoebic meningoencephalitis, a fatal disease in the central nervous system. This study aims to explore the roles of -derived EVs (-EVs) in host-pathogen interactions using the THP-1 cell line as a model. The -EVs were isolated from the trophozoite culture supernatant using sequential centrifugation and characterized by nanoparticle tracking analysis and transmission electron microscopy. The functional roles of -EVs in the apoptosis and immune response induction of THP-1 monocytes and macrophages were examined by flow cytometry, quantitative PCR, and ELISA. Results showed that -EVs displayed vesicles with bilayer membrane structure approximately 130-170 nm in diameter. The -EVs can be internalized by macrophages and induce macrophage responses by induction of the expression of costimulatory molecules CD80, CD86, HLA-DR, and CD169 and the production of cytokine IL-8. However, -EVs did not affect the apoptosis of macrophages. These findings illustrate the potential role of -EVs in mediating the host immune cell activation and disease pathogenesis.
致病原生动物释放的细胞外囊泡(EVs)在宿主 - 寄生虫通讯和疾病发病机制中起关键作用。是一种导致原发性阿米巴脑膜脑炎的自由生活原生动物,这是一种中枢神经系统的致命疾病。本研究旨在以THP - 1细胞系为模型,探索[具体原生动物名称]来源的EVs([具体原生动物名称] - EVs)在宿主 - 病原体相互作用中的作用。通过连续离心从[具体原生动物名称]滋养体培养上清液中分离出[具体原生动物名称] - EVs,并通过纳米颗粒跟踪分析和透射电子显微镜进行表征。通过流式细胞术、定量PCR和ELISA检测了[具体原生动物名称] - EVs在THP - 1单核细胞和巨噬细胞凋亡及免疫反应诱导中的功能作用。结果表明,[具体原生动物名称] - EVs呈现出直径约为130 - 170 nm的具有双层膜结构的囊泡。[具体原生动物名称] - EVs可被巨噬细胞内化,并通过诱导共刺激分子CD80、CD86、HLA - DR和CD169的表达以及细胞因子IL - 8的产生来诱导巨噬细胞反应。然而,[具体原生动物名称] - EVs不影响巨噬细胞的凋亡。这些发现说明了[具体原生动物名称] - EVs在介导宿主免疫细胞激活和疾病发病机制中的潜在作用。 (注:原文中部分[具体原生动物名称]未明确写出,翻译时保留原文形式)