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一种钙依赖性蛋白激酶调节疟原虫动合子进入中肠上皮细胞的过程。

A calcium-dependent protein kinase regulates Plasmodium ookinete access to the midgut epithelial cell.

作者信息

Ishino Tomoko, Orito Yuki, Chinzei Yasuo, Yuda Masao

机构信息

Department of Medical Zoology, Mie University School of Medicine, Edobashi, Tsu, Mie 514-0001, Japan.

出版信息

Mol Microbiol. 2006 Feb;59(4):1175-84. doi: 10.1111/j.1365-2958.2005.05014.x.

Abstract

Plasmodium parasites are fertilized in the mosquito midgut and develop into motile zygotes, called ookinetes, which invade the midgut epithelium. Here we show that a calcium-dependent protein kinase, CDPK3, of the rodent malarial parasite (Plasmodium berghei) is produced in the ookinete stage and has a critical role in parasite transmission to the mosquito vector. Targeted disruption of the CDPK3 gene decreased ookinete ability to infect the mosquito midgut by nearly two orders of magnitude. Electron microscopic analyses demonstrated that the disruptant ookinetes could not access midgut epithelial cells by traversing the layer covering the cell surface. An in vitro migration assay showed that these ookinetes lack the ability to migrate through an artificial gel, suggesting that this defect caused their failure to access the epithelium. In vitro migration assays also suggested that this motility is induced in the wild type by mobilization of intracellular stored calcium. These results indicate that a signalling pathway involving calcium and CDPK3 regulates ookinete penetration of the layer covering the midgut epithelium. Because humans do not possess CDPK family proteins, CDPK3 is a good target for blocking malarial transmission to the mosquito vector.

摘要

疟原虫在蚊子的中肠内受精并发育成活动的合子,称为动合子,动合子会侵入中肠上皮。我们在此表明,啮齿动物疟原虫(伯氏疟原虫)的一种钙依赖性蛋白激酶CDPK3在动合子阶段产生,并且在疟原虫传播至蚊子媒介过程中起关键作用。对CDPK3基因进行靶向破坏使动合子感染蚊子中肠的能力降低了近两个数量级。电子显微镜分析表明,被破坏的动合子无法穿过覆盖细胞表面的层进入中肠上皮细胞。体外迁移试验表明,这些动合子缺乏穿过人工凝胶迁移的能力,这表明该缺陷导致它们无法进入上皮。体外迁移试验还表明,野生型中的这种运动性是由细胞内储存钙的动员诱导的。这些结果表明,涉及钙和CDPK3的信号通路调节动合子对覆盖中肠上皮的层的穿透。由于人类不具有CDPK家族蛋白,因此CDPK3是阻断疟原虫向蚊子媒介传播的良好靶点。

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