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首页> 外文期刊>The Journal of biological chemistry >Role of Plasmodium berghei cGMP-dependent Protein Kinase in Late Liver Stage Development
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Role of Plasmodium berghei cGMP-dependent Protein Kinase in Late Liver Stage Development

机译:Plasmodium Berghei CGMP依赖性蛋白激酶在晚肝阶段发展中的作用

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摘要

The liver is the first organ infected by Plasmodium sporozoites during malaria infection. In the infected hepatocytes, sporozoites undergo a complex developmental program to eventually generate hepatic merozoites that are released into the bloodstream in membrane-bound vesicles termed merosomes. Parasites blocked at an early developmental stage inside hepatocytes elicit a protective host immune response, making them attractive targets in the effort to develop a pre-erythrocytic stage vaccine. Here, we generated parasites blocked at a late developmental stage inside hepatocytes by conditionally disrupting the Plasmodium berghei cGMP-dependent protein kinase in sporozoites. Mutant sporozoites are able to invade hepatocytes and undergo intracellular development. However, they remain blocked as late liver stages that do not release merosomes into the medium. These late arrested liver stages induce protection in immunized animals. This suggests that, similar to the well studied early liver stages, late stage liver stages too can confer protection from sporozoite challenge.
机译:肝脏是在疟疾感染期间被疟原虫孢子感染的第一个器官。在受感染的肝细胞中,孢子生殖性经历复杂的发育方案,最终产生肝脏混血,其被释放到膜结合囊泡中称为Merosomes的血液中。寄生虫在肝细胞内部的早期发育阶段引发了一种保护宿主免疫应答,使其具有有吸引力的旨在开发出开发性疫苗的疫苗。在这里,我们通过条件破坏孢子中的孢子素依赖于孢子素依赖于孢子蛋白依赖于孢子蛋白依赖于肝细胞的血浆依赖性蛋白激酶,产生寄生虫。突变孢子能够侵入肝细胞并经历细胞内发育。然而,它们保持被阻止为晚期肝脏阶段,这些肝脏阶段不会将Merosomes释放到培养基中。这些晚期被捕的肝脏阶段在免疫动物诱导保护。这表明,类似于研究的早期肝脏阶段,晚期肝脏阶段也可以赋予孢子唑挑战的保护。

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