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Meningococcal Outer Membrane Protein NhhA Triggers Apoptosis in Macrophages

机译:脑膜炎球菌外膜蛋白NhhA触发巨噬细胞凋亡。

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Phagocytotic cells play a fundamental role in the defense against bacterial pathogens. One mechanism whereby bacteria evade phagocytosis is to produce factors that trigger apoptosis. Here we identify for the first time a meningococcal protein capable of inducing macrophage apoptosis. The conserved meningococcal outer membrane protein NhhA (Neisseria hia/hsf homologue A, also known as Hsf) mediates bacterial adhesion and interacts with extracellular matrix components heparan sulphate and laminin. Meningococci lacking NhhA fail to colonise nasal mucosa in a mouse model of meningococcal disease. We found that exposure of macrophages to NhhA resulted in a highly increased rate of apoptosis that proceeded through caspase activation. Exposure of macrophages to NhhA also led to iNOS induction and nitric oxide production. However, neither nitric oxide production nor TNF-α signaling was found to be a prerequisite for NhhA-induced apoptosis. Macrophages exposed to wildtype NhhA-expressing meningococci were also found to undergo apoptosis whereas NhhA-deficient meningococci had a markedly decreased capacity to induce macrophage apoptosis. These data provide new insights on the role of NhhA in meningococcal disease. NhhA-induced macrophage apoptosis could be a mechanism whereby meningococci evade immunoregulatory and phagocytotic actions of macrophages.
机译:吞噬细胞在防御细菌病原体中起着基本作用。细菌逃避吞噬作用的一种机制是产生触发凋亡的因子。在这里,我们首次鉴定出能够诱导巨噬细胞凋亡的脑膜炎球菌蛋白。保守的脑膜炎球菌外膜蛋白NhhA(奈瑟氏菌hia / hsf同源物A,也称为Hsf)介导细菌粘附并与细胞外基质成分硫酸乙酰肝素和层粘连蛋白相互作用。缺乏NhhA的脑膜炎球菌在脑膜炎球菌疾病的小鼠模型中无法在鼻粘膜上定殖。我们发现巨噬细胞暴露于NhhA导致通过caspase激活进行凋亡的高度增加。巨噬细胞暴露于NhhA也导致iNOS诱导和一氧化氮生成。然而,一氧化氮的产生和TNF-α信号均不是NhhA诱导的凋亡的先决条件。还发现暴露于野生型表达NhhA的脑膜炎球菌的巨噬细胞发生凋亡,而缺乏NhhA的脑膜炎球菌诱导巨噬细胞凋亡的能力明显降低。这些数据提供了有关NhhA在脑膜炎球菌疾病中的作用的新见解。 NhhA诱导巨噬细胞凋亡可能是脑膜炎球菌逃避巨噬细胞免疫调节和吞噬作用的机制。

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