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首页> 外文期刊>Infection and immunity >Anthrax Lethal Toxin Impairs CD1d-Mediated Antigen Presentation by Targeting the Extracellular Signal-Related Kinase 1/2 Mitogen-Activated Protein Kinase Pathway
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Anthrax Lethal Toxin Impairs CD1d-Mediated Antigen Presentation by Targeting the Extracellular Signal-Related Kinase 1/2 Mitogen-Activated Protein Kinase Pathway

机译:炭疽致死性毒素通过靶向细胞外信号相关激酶1/2丝裂原活化的蛋白激酶途径来破坏CD1d介导的抗原呈递。

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Lethal toxin (LT) is a critical virulence factor of Bacillus anthracis and an important means by which this bacterium evades the host's immune system. In this study, we demonstrate that CD1d-expressing cells treated with LT have reduced CD1d-mediated antigen presentation. We earlier showed an important role for the mitogen-activated protein kinase extracellular signal-regulated kinase 1/2 (ERK1/2) in the regulation of CD1d-mediated antigen presentation, and we report here that LT impairs antigen presentation by CD1d in an ERK1/2-dependent manner. Similarly, LT and the ERK1/2 pathway-specific inhibitor U0126 caused a decrease in major histocompatibility complex (MHC) class II-mediated antigen presentation. Confocal microscopy analyses revealed altered intracellular distribution of CD1d and LAMP-1 in LT-treated cells, similar to the case for ERK1/2-inhibited cells. These results suggest that Bacillus anthracis has the ability to evade the host's innate immune system by reducing CD1d-mediated antigen presentation through targeting the ERK1/2 pathway.
机译:致死毒素(LT)是炭疽杆菌的重要毒力因子,也是该细菌逃避宿主免疫系统的重要手段。在这项研究中,我们证明用LT处理的CD1d表达细胞减少了CD1d介导的抗原呈递。我们之前显示了有丝分裂原激活的蛋白激酶细胞外信号调节激酶1/2(ERK1 / 2)在CD1d介导的抗原呈递的调节中的重要作用,并且我们在此报告LT损害了ERK1中CD1d的抗原呈递。 / 2依赖方式。同样,LT和ERK1 / 2途径特异性抑制剂U0126导致主要组织相容性复合物(MHC)II类介导的抗原呈递减少。共聚焦显微镜分析显示,经LT处理的细胞中CD1d和LAMP-1的胞内分布发生了变化,类似于ERK1 / 2抑制细胞的情况。这些结果表明炭疽杆菌具有通过靶向ERK1 / 2途径减少CD1d介导的抗原呈递来逃避宿主先天免疫系统的能力。

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