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A host cell membrane microdomain is a critical factor for organelle discharge by Toxoplasma gondii

机译:宿主细胞膜微区是弓形虫细胞器释放的关键因素

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Host cell microdomains are involved in the attachment, entry, and replication of intracellular microbial pathogens. Entry into the host cell of Toxoplasma gondii and the subsequent survival of this protozoan parasite are tightly coupled with the proteins secreted from organelle called rhoptry. The rhoptry proteins are rapidly discharged into clusters of vesicles, called evacuoles, which are then delivered to parasitophorous vacuoles (PVs) or nucleus. In this study, we examined the roles of two host cell microdomain components, cholesterol and glycosylphosphatidylinositol (GPI), in evacuole formation. The acute depletion of cholesterol from the host cell plasma membrane blocked evacuole formation but not invasion. Whereas the lack of host cell GPI also altered evacuole formation but not invasion, instead inducing excess evacuole formation. The latter effect was not influenced by the evacuole-inhibiting effects of host cell cholesterol depletion, indicating the independent roles of host GPI and cholesterol in evacuole formation. In addition, the excess formation of evacuoles resulted in the enhanced recruitment of host mitochondria and endoplasmic reticulum to PVs, which in turn stimulated the growth of the parasite. (C) 2016 The Authors. Published by Elsevier Ireland Ltd. This is an open access article under the CC BY-NC-ND license.
机译:宿主细胞微区参与细胞内微生物病原体的附着,进入和复制。进入弓形虫的宿主细胞以及该原生动物寄生虫的随后存活与细胞器分泌的称为rhoptry的蛋白质紧密结合。重组蛋白迅速排入称为疏液的囊泡簇,然后被送到寄生虫的液泡(PVs)或细胞核中。在这项研究中,我们检查了两个宿主细胞微区成分,胆固醇和糖基磷脂酰肌醇(GPI)在疏散形成中的作用。来自宿主细胞质膜的胆固醇的急性消耗阻止了疏散的形成,但没有阻止入侵。而缺乏宿主细胞的GPI也改变了疏散形成,但没有改变侵袭,而是诱导了过多的疏散形成。后者的作用不受宿主细胞胆固醇消耗的排空抑制作用的影响,表明宿主GPI和胆固醇在排空形成中的独立作用。此外,疏散的过量形成导致宿主线粒体和内质网向PV的增加募集,进而刺激了寄生虫的生长。 (C)2016作者。由Elsevier Ireland Ltd.发布。这是CC BY-NC-ND许可下的开放获取文章。

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