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首页> 外文期刊>Cellular microbiology >Insights into endosomal maturation of human holo-transferrin in the enteric parasite Entamoeba histolytica: essential roles of Rab7A and Rab5 in biogenesis of giant early endocytic vacuoles
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Insights into endosomal maturation of human holo-transferrin in the enteric parasite Entamoeba histolytica: essential roles of Rab7A and Rab5 in biogenesis of giant early endocytic vacuoles

机译:人全转铁蛋白在肠寄生虫组织变形虫中的内体成熟的见解:Rab7A和Rab5在巨大的早期内吞空泡的生物发生中的重要作用。

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摘要

The pathogenic amoeba Entamoeba histolytica is one of the causative agents of health hazards in tropical countries. It causes amoebic dysentery, colitis and liver abscesses in human. Iron is one of the essential nutritional resources for survival and chronic infection caused by the amoeba. The parasite has developed multiple ways to import, sequester and utilize iron from various iron-binding proteins from its host. In spite of its central role in pathogenesis, the mechanism of iron uptake by the parasite is largely unknown. Here, we carried out a systematic study to understand the role of some of the amoebic homologues of mammalian endocytic Rab GTPases (Rab5 and Rab21, Rab7A and Rab7B) in intracellular transport of human holo-transferrin by the parasite. Flow cytometry and quantitative microscopic image analysis revealed that Rab5 and Rab7A are required for the biogenesis of amoebic giant endocytic vacuoles (GEVs) and regulate the early phase of intracellular trafficking of transferrin. Rab7B is involved in the late phase, leading to the degradation of transferrin in the amoebic lysosome-like compartments. Using time-lapse fluorescence imaging in fixed trophozoites, we determined the kinetics of the vesicular transport of transferrin through Rab5-, Rab7A- and Rab7B-positive compartments. The involvement of Rab7A in the early phase of endocytosis by the parasite marks a significant divergence from its host in terms of spatiotemporal regulation by the Rab GTPases.
机译:致病性变形虫阿米巴变形杆菌是热带国家健康危害的致病因素之一。它会在人体内引起阿米巴痢疾,结肠炎和肝脓肿。铁是变形虫引起的生存和慢性感染的重要营养资源之一。该寄生虫已开发出多种方式,可从其宿主中导入,螯合和利用来自各种铁结合蛋白的铁。尽管其在发病机理中起着重要作用,但寄生虫摄取铁的机制仍是未知之数。在这里,我们进行了系统的研究,以了解哺乳动物内吞Rab GTPases(Rab5和Rab21,Rab7A和Rab7B)的某些厌氧同源物在人全转铁蛋白通过寄生虫的细胞内转运中的作用。流式细胞仪和定量显微镜图像分析显示,Rab5和Rab7A是阿米巴巨噬细胞内吞空泡(GEV)的生物合成所必需的,并调节转铁蛋白在细胞内运输的早期阶段。 Rab7B参与晚期,导致在阿米巴溶酶体样区室中转铁蛋白的降解。使用固定滋养体中的延时荧光成像,我们确定了运铁蛋白通过Rab5-,Rab7A-和Rab7B阳性区室的囊泡转运动力学。在Rab GTPases的时空调节方面,Rab7A参与了内吞作用的早期阶段,标志着它与宿主的显着不同。

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