首页> 美国卫生研究院文献>Infection and Immunity >Apical Organelle Discharge by Cryptosporidium parvum Is Temperature Cytoskeleton and Intracellular Calcium Dependent and Required for Host Cell Invasion
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Apical Organelle Discharge by Cryptosporidium parvum Is Temperature Cytoskeleton and Intracellular Calcium Dependent and Required for Host Cell Invasion

机译:细小隐孢子虫的根尖细胞器放电是温度细胞骨架和细胞内钙依赖的并且是宿主细胞入侵所必需的

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摘要

The apical organelles in apicomplexan parasites are characteristic secretory vesicles containing complex mixtures of molecules. While apical organelle discharge has been demonstrated to be involved in the cellular invasion of some apicomplexan parasites, including Toxoplasma gondii and Plasmodium spp., the mechanisms of apical organelle discharge by Cryptosporidium parvum sporozoites and its role in host cell invasion are unclear. Here we show that the discharge of C. parvum apical organelles occurs in a temperature-dependent fashion. The inhibition of parasite actin and tubulin polymerization by cytochalasin D and colchicines, respectively, inhibited parasite apical organelle discharge. Chelation of the parasite's intracellular calcium also inhibited apical organelle discharge, and this process was partially reversed by raising the intracellular calcium concentration by use of the ionophore A23187. The inhibition of parasite cytoskeleton polymerization by cytochalasin D and colchicine and the depletion of intracellular calcium also decreased the gliding motility of C. parvum sporozoites. Importantly, the inhibition of apical organelle discharge by C. parvum sporozoites blocked parasite invasion of, but not attachment to, host cells (i.e., cultured human cholangiocytes). Moreover, the translocation of a parasite protein, CP2, to the host cell membrane at the region of the host cell-parasite interface was detected; an antibody to CP2 decreased the C. parvum invasion of cholangiocytes. These data demonstrate that the discharge of C. parvum sporozoite apical organelle contents occurs and that it is temperature, intracellular calcium, and cytoskeleton dependent and required for host cell invasion, confirming that apical organelles play a central role in C. parvum entry into host cells.
机译:apicomplexan寄生虫中的顶端细胞器是特征性的分泌性囊泡,包含复杂的分子混合物。虽然已经证明顶细胞器放电参与了一些蚜虫复合体寄生虫的细胞入侵,包括弓形虫和疟原虫,但是隐球孢子虫子孢子顶细胞器放电的机制及其在宿主细胞入侵中的作用尚不清楚。在这里,我们显示C. parvum根尖细胞器的放电以温度依赖性方式发生。细胞松弛素D和秋水仙碱分别抑制寄生虫肌动蛋白和微管蛋白聚合,从而抑制了寄生虫的顶端细胞器放电。寄生虫细胞内钙的螯合也抑制了顶端细胞器的排出,通过使用离子载体A23187提高细胞内钙浓度,可部分逆转此过程。细胞松弛素D和秋水仙碱对寄生虫细胞骨架聚合的抑制作用以及细胞内钙的消耗也降低了小球藻子孢子的滑行能力。重要的是,细小隐孢子虫子孢子对顶端细胞器放电的抑制阻止了宿主细胞(即培养的人胆管细胞)的寄生虫入侵,但没有附着。此外,还检测到了寄生虫蛋白CP2在宿主细胞-寄生虫界面区域内转移到宿主细胞膜上。抗CP2的抗体可减少细小梭菌对胆管细胞的侵袭。这些数据表明,发生了细小隐孢子虫根尖细胞器内容物的释放,并且它是温度,细胞内钙和细胞骨架的依赖性,并且是宿主细胞入侵所必需的,这证实了根尖细胞器在细小隐孢子虫进入宿主细胞中起着核心作用。 。

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