Departamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Mexico City, Mexico.
Front Cell Infect Microbiol. 2018 Aug 24;8:295. doi: 10.3389/fcimb.2018.00295. eCollection 2018.
, the causal agent of human amoebiasis, has two morphologically different phases: a resistant cyst and a trophozoite responsible for the invasion of the host tissues such as the colonic mucosa and the intestinal epithelium. During migration, trophozoites usually produce protuberances such as pseudopods and rarely filopodia, structures that have been observed in the interaction of trophozoites with human colonic epithelial tissue. To study the different membrane projections produced by the trophozoites, including pseudopods, filopodia, uropods, blebs, and others, we designed an induction system using erythrocyte extract or fibronectin (FN) in micropatterned grill lines (each micro-line containing multiple micro-portions of FN or erythrocyte extract) on which the trophozoites were placed in culture for migration assays. Using light, confocal, and scanning electron microscopy, we established that trophozoites frequently produce short and long filopodia, large retractile uropods in the rear, pseudopods, blebs, and others structures, also showing continuous migration periods. The present study provides a simple migration method to induce trophozoites to generate abundant membrane protrusion structures that are rarely obtained in normal or induced cultures, such as long filopodia; this method will allow a-better understanding of the interactions of trophozoites with FN and cell debris. trophozoites motility plays an important role in invasive amoebiasis. It has been proposed that both physical forces and chemical signals are involved in the trophozoite motility and migration. However, the molecules that drive the chemotactic migration remain to be determined. We propose the present assay to study host molecules that guide chemotactic behavior because the method is highly reproducible, and a live image of cell movement and migration can be quantified.
溶组织内阿米巴,人类阿米巴病的病原体,有两种形态上不同的阶段:抗性囊和滋养体,负责侵袭宿主组织,如结肠黏膜和肠上皮。在迁移过程中,滋养体通常会产生突起,如伪足和很少的丝状伪足,这些结构在滋养体与人类结肠上皮组织的相互作用中已经观察到。为了研究滋养体产生的不同膜突起,包括伪足、丝状伪足、尾足、泡囊和其他结构,我们设计了一个诱导系统,使用红细胞提取物或纤连蛋白(FN)在微图案格栅线(每条微线包含多个 FN 或红细胞提取物的微部分)上,将滋养体放在培养物中进行迁移分析。使用光、共聚焦和扫描电子显微镜,我们确定滋养体经常产生短的和长的丝状伪足、后部大的可回缩尾足、伪足、泡囊和其他结构,也显示出连续的迁移期。本研究提供了一种简单的迁移方法,可诱导滋养体产生丰富的膜突起结构,这些结构在正常或诱导培养中很少获得,如长丝状伪足;这种方法将使我们更好地了解滋养体与 FN 和细胞碎片的相互作用。滋养体的运动在侵袭性阿米巴病中起着重要作用。有人提出,物理力和化学信号都参与了滋养体的运动和迁移。然而,驱动趋化性迁移的 分子仍有待确定。我们提出本实验来研究指导趋化行为的宿主分子,因为该方法具有高度的可重复性,可以定量分析细胞运动和迁移的实时图像。