Department of Microbiology and Molecular Genetics, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, New Jersey 07103, USA.
J Biol Chem. 2010 Jan 29;285(5):3282-8. doi: 10.1074/jbc.M109.070367. Epub 2009 Nov 24.
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.
肝脏是疟原虫感染时疟原虫孢子首先感染的器官。在受感染的肝细胞中,孢子经历一个复杂的发育程序,最终产生肝裂殖子,它们在称为 merosomes 的膜结合囊泡中释放到血液中。在肝细胞内发育早期被阻断的寄生虫会引发保护性宿主免疫反应,因此成为开发红细胞前期疫苗的有吸引力的靶点。在这里,我们通过条件性破坏疟原虫 cGMP 依赖性蛋白激酶使孢子内的疟原虫在发育后期被阻断。突变的孢子能够侵入肝细胞并进行细胞内发育。然而,它们作为晚期肝阶段被阻断,不会将 merosomes 释放到培养基中。这些晚期被阻断的肝阶段在免疫动物中诱导保护。这表明,与研究得很好的早期肝阶段相似,晚期肝阶段也可以提供对孢子挑战的保护。