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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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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。虽然已证明顶端细胞器放电与某些寄生虫寄生虫,包括 Tondoplasma gondii Plasmodium spp。的细胞入侵有关,但的顶端细胞器放电机制小隐孢子虫子孢子及其在宿主细胞侵袭中的作用尚不清楚。在这里,我们显示了 C的放电。小顶细胞器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了寄生虫肌动蛋白和微管蛋白的聚合,从而抑制了寄生虫的根尖细胞器放电。寄生虫的细胞内钙的螯合也抑制了根尖细胞器的排出,通过使用离子载体A23187提高细胞内钙的浓度,这一过程被部分逆转。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 C的滑行能力。小孢子虫。重要的是, C对根尖细胞器放电的抑制。小孢子虫阻断了寄生虫对宿主细胞(即培养的人胆管细胞)的侵袭,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的抗体可降低 C。小卵对胆管细胞的侵袭这些数据表明 C的放电。小孢子虫的根尖细胞器含量随温度,细胞内钙和细胞骨架的变化而变化,是宿主细胞入侵所必需的,这证明根尖细胞器在 C中起着核心作用。进入宿主细胞。

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