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首页> 外文期刊>Journal of Immunological Methods >An immunoradiometric assay for the quantification of Plasmodium sporozoite invasion of HepG2 cells.
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An immunoradiometric assay for the quantification of Plasmodium sporozoite invasion of HepG2 cells.

机译:一种用于定量分析疟原虫子孢子侵袭HepG2细胞的免疫放射分析方法。

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摘要

Malaria infection in a vertebrate host is initiated when Plasmodium sporozoites invade hepatocytes after injection by an infected mosquito. In vitro, the parasites invade and develop in HepG2 cells and these cells have been used to study target cell invasion by sporozoites. Previously described in vitro invasion assays involve staining and counting of intracellular sporozoites or exoerythrocytic forms of the parasite. Here we describe an immunoradiometric assay that can quantify sporozoite invasion of HepG2 cells in vitro. The assay relies on the differential detection of intracellular and extracellular circumsporozoite protein (CS; the major surface protein of the sporozoite) which can then be used to calculate the efficiency of invasion. Since this assay can be performed more rapidly than the current assays in which parasites must be counted under a microscope, it enables investigators to more rapidly screen inhibitors of sporozoite invasion.
机译:当疟原虫子孢子虫被感染的蚊子注射后侵入肝细胞时,就会在脊椎动物宿主中引发疟疾感染。在体外,该寄生虫侵入并在HepG2细胞中发育,这些细胞已用于研究子孢子对靶细胞的侵袭。先前描述的体外侵袭测定涉及对寄生虫的胞内子孢子或外红细胞形式的染色和计数。在这里,我们描述了一种免疫放射测定法,可以定量地体外对子孢子侵染HepG2细胞。该测定法依赖于细胞内和细胞外环子孢子蛋白(CS;子孢子的主要表面蛋白)的差异检测,然后可用于计算入侵效率。由于该检测方法可以比目前必须在显微镜下计数寄生虫的检测方法进行得更快,因此它使研究人员可以更快地筛选子孢子入侵的抑制剂。

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