State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, CAAS, Lanzhou 730046, China.
College of Life Science and Technology, Xinjiang University, Urumqi 830046, China.
Acta Trop. 2021 Jan;213:105756. doi: 10.1016/j.actatropica.2020.105756. Epub 2020 Nov 13.
Extracellular vesicles (EVs) are heterogeneous populations of different membrane-wrapped vesicles in size and encapsulated cargo and have recently emerged as a crucial carrier with the functions in intercellular communication, being involved in host-parasite interactions. However, Echinococcus granulosus EVs are not fully described. To separate EVs with a different size, the culture supernatant of E. granulosus protoscoleces (PSCs) was sequentially centrifuged at 2,000g, 10,000g and 110,000g, and the resulting precipitates were accordingly named as 2K, 10K and 110K EVs, respectively. The size and morphology of three different EVs were identified using ZETASIZER NANO and transmission electron microscopy (TEM), respectively. Then mass spectrometry was applied to define protein cargo of EVs and EV internalization was assessed using fluorescent microscopy and flow cytometry. The results showed that 2K EVs mainly ranged from 450 to 950 nm in diameter, 10K EVs ranged from 220 to 390 nm and 110K EVs from 60 to 150 nm. A total of 901 EV proteins were identified, 328 of which were commonly found in the three types of EVs. GO analysis revealed that these proteins were mainly involved in binding (44%) and catalytic activity (44%). Three types of EVs were different in biomarkers (Enolase and 14-3-3) and in reactivity with anti-echinococcosis positive serum. Moreover, 110K EVs were more easily internalized by hepatic cells than 10K EVs as well as 2K EVs (p < 0.0001). These results reveal the physical and biological discrepancy among 2K, 10K and 110K EVs, suggesting a distinct role in host-parasite interactions.
细胞外囊泡 (EVs) 是不同大小的、具有膜包裹的囊泡的异质群体,并且囊封了货物,最近作为细胞间通讯的重要载体出现,参与了宿主-寄生虫相互作用。然而,细粒棘球蚴 EVs 尚未得到充分描述。为了分离不同大小的 EVs,将细粒棘球蚴原头节 (PSCs) 的培养上清液依次在 2000g、10000g 和 110000g 下离心,所得沉淀物分别命名为 2K、10K 和 110K EVs。使用 ZETASIZER NANO 和透射电子显微镜 (TEM) 分别鉴定了三种不同 EVs 的大小和形态。然后应用质谱法定义 EV 的蛋白质货物,并通过荧光显微镜和流式细胞术评估 EV 的内化。结果表明,2K EVs 主要直径范围为 450 至 950nm,10K EVs 直径范围为 220 至 390nm,110K EVs 直径范围为 60 至 150nm。共鉴定出 901 种 EV 蛋白,其中 328 种在三种类型的 EV 中均有发现。GO 分析显示,这些蛋白主要参与结合(44%)和催化活性(44%)。三种类型的 EV 在生物标志物(烯醇酶和 14-3-3)和与抗包虫病阳性血清的反应性方面存在差异。此外,110K EVs 比 10K EVs 以及 2K EVs 更容易被肝细胞内化(p < 0.0001)。这些结果揭示了 2K、10K 和 110K EVs 之间的物理和生物学差异,表明它们在宿主-寄生虫相互作用中具有不同的作用。