首页> 美国卫生研究院文献>Infection and Immunity >Pasteurella multocida Toxin Activates Human Monocyte-Derived and Murine Bone Marrow-Derived Dendritic Cells In Vitro but Suppresses Antibody Production In Vivo
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Pasteurella multocida Toxin Activates Human Monocyte-Derived and Murine Bone Marrow-Derived Dendritic Cells In Vitro but Suppresses Antibody Production In Vivo

机译:多杀性巴氏杆菌毒素体外激活人单核细胞衍生和鼠骨髓衍生树突状细胞但抑制体内抗体产生。

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摘要

Pasteurella multocida toxin (PMT) is a potent mitogen for fibroblasts and osteoblastic cells. PMT activates phospholipase C-β through Gqα, and the activation of this pathway is responsible for its mitogenic activity. Here, we investigated the effects of PMT on human monocyte-derived dendritic cells (MDDC) in vitro and show a novel activity for PMT. In this regard, PMT activates MDDC to mature in a dose-dependent manner through the activation of phospholipase C and subsequent mobilization of calcium. This activation was accompanied by enhanced stimulation of naïve alloreactive T cells and dominant inhibition of interleukin-12 production in the presence of saturating concentrations of lipopolysaccharide. Surprisingly, although PMT mimics the activating effects of cholera toxin on human MDDC and mouse bone marrow-derived dendritic cells, we found that PMT is not a mucosal adjuvant and that it suppresses the adjuvant effects of cholera toxin in mice. Together, these results indicate discordant effects for PMT in vitro compared to those in vivo.
机译:多杀性巴斯德氏菌毒素(PMT)是成纤维细胞和成骨细胞的有效促分裂原。 PMT通过Gqα激活磷脂酶C-β,该途径的激活为其促有丝分裂活性负责。在这里,我们调查了PMT对人单核细胞衍生树突状细胞(MDDC)的影响,并显示了PMT的新活性。在这方面,PMT通过激活磷脂酶C和随后的钙动员,以剂量依赖的方式激活MDDC使其成熟。在饱和浓度的脂多糖存在下,这种激活伴随着对幼稚的同种反应性T细胞的刺激增强和对白介素12产生的显着抑制。出人意料的是,尽管PMT模仿了霍乱毒素对人MDDC和小鼠骨髓来源的树突状细胞的激活作用,但我们发现PMT并不是粘膜佐剂,它可以抑制小鼠霍乱毒素的佐剂作用。在一起,这些结果表明与体内的PMT相比,体外PMT的效果不一致。

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