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Development of the Cellular Immune System of Drosophila Requires the Membrane Attack Complex/Perforin-Like Protein Torso-Like

机译:果蝇细胞免疫系统的发展需要膜攻击复合物/穿孔素样蛋白躯干样。

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摘要

Pore-forming members of the membrane attack complex/perforin-like (MACPF) protein superfamily perform well-characterized roles as mammalian immune effectors. For example, complement component 9 and perforin function to directly form pores in the membrane of Gram-negative pathogens or virally infected/transformed cells, respectively. In contrast, the only known MACPF protein in Drosophila melanogaster, Torso-like, plays crucial roles during development in embryo patterning and larval growth. Here, we report that in addition to these functions, Torso-like plays an important role in Drosophila immunity. However, in contrast to a hypothesized effector function in, for example, elimination of Gram-negative pathogens, we find that null mutants instead show increased susceptibility to certain Gram-positive pathogens such as Staphylococcus aureus and Enterococcus faecalis. We further show that this deficit is due to a severely reduced number of circulating immune cells and, as a consequence, an impaired ability to phagocytose bacterial particles. Together these data suggest that Torso-like plays an important role in controlling the development of the Drosophila cellular immune system.
机译:膜攻击复合物/类穿孔素(MACPF)蛋白超家族的毛孔形成成员作为哺乳动物的免疫效应子发挥了很好的作用。例如,补体成分9和穿孔素分别在革兰氏阴性病原体或病毒感染/转化的细胞的膜中直接形成孔。相比之下,果蝇中唯一已知的MACPF蛋白(躯干)在胚胎形成和幼虫生长的发育过程中起着至关重要的作用。在这里,我们报告说,除了这些功能,类躯干在果蝇免疫中也起着重要作用。但是,与假设的效应子功能(例如在消除革兰氏阴性病原体中)相反,我们发现无效突变体显示出对某些革兰氏阳性病原体(如金黄色葡萄球菌和粪肠球菌)的敏感性增加。我们进一步表明,这种缺陷是由于循环免疫细胞的数量严重减少,因此吞噬细菌颗粒的能力受损。这些数据一起表明,躯干样蛋白在控制果蝇细胞免疫系统的发育中起着重要作用。

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