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疟原虫子孢子中一种带有膜攻击复合物结构域的蛋白质,是在感染肝细胞之前突破肝血窦细胞层所必需的。

A Plasmodium sporozoite protein with a membrane attack complex domain is required for breaching the liver sinusoidal cell layer prior to hepatocyte infection.

作者信息

Ishino Tomoko, Chinzei Yasuo, Yuda Masao

机构信息

Mie University School of Medicine, Mie, Japan.

出版信息

Cell Microbiol. 2005 Feb;7(2):199-208. doi: 10.1111/j.1462-5822.2004.00447.x.

Abstract

Plasmodium sporozoites are injected into the mammalian host during mosquito blood feeding and carried by the blood stream to the liver, where they infect hepatocytes and develop into erythrocyte-invasive forms. To reach the hepatocytes, sporozoites must cross the liver sinusoidal cell layer, which separates the hepatocytes from the circulatory system. Little is known about the molecular mechanisms by which sporozoites breach this cellular barrier. Here we report that a protein with a membrane attack complex/perforin (MACPF)-related domain is involved in this step. This molecule is specifically expressed in liver-infective sporozoites and localized in micronemes, organelles engaged in host cell invasion. Gene disruption experiments revealed that this protein is essential for the membrane-wounding activity of the sporozoite and is involved in its traversal of the sinusoidal cell layer prior to hepatocyte-infection. Disruptants failed to leave the circulation, and most of them were eliminated from the blood by liver perfusion. Our results suggest that rupture of the host plasma membrane by the pore-forming activity of this molecule is essential for cell passage of the sporozoite. This report is the first to demonstrate an important role of a MACPF-related protein in host cell invasion by a pathogenic microorganism.

摘要

疟原虫子孢子在蚊子吸食血液时被注入哺乳动物宿主,并通过血流被带到肝脏,在那里它们感染肝细胞并发育成侵入红细胞的形式。为了到达肝细胞,子孢子必须穿过肝血窦细胞层,该层将肝细胞与循环系统分隔开来。关于子孢子突破这一细胞屏障的分子机制知之甚少。在此我们报告,一种具有膜攻击复合物/穿孔素(MACPF)相关结构域的蛋白质参与了这一步骤。该分子在感染肝脏的子孢子中特异性表达,并定位于微线体,微线体是参与宿主细胞入侵的细胞器。基因敲除实验表明,该蛋白质对子孢子的膜损伤活性至关重要,并参与其在感染肝细胞之前穿过血窦细胞层的过程。基因敲除体无法离开循环系统,其中大多数通过肝脏灌注从血液中清除。我们的结果表明,该分子的成孔活性导致宿主质膜破裂对子孢子的细胞通过至关重要。本报告首次证明了MACPF相关蛋白在病原微生物入侵宿主细胞中的重要作用。

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