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Porphyromonas gingivalis Gingipains Trigger a Proinflammatory Response in Human Monocyte-derived Macrophages Through the p38α Mitogen-activated Protein Kinase Signal Transduction Pathway

机译:牙龈卟啉单胞菌姜黄素通过p38α丝裂原活化蛋白激酶信号转导途径触发人单核细胞衍生巨噬细胞的促炎反应。

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摘要

Porphyromonas gingivalis, the major etiologic agent of chronic periodontitis, produces a broad spectrum of virulence factors, including Arg- and Lys-gingipain cysteine proteinases. In this study, we investigated the capacity of P. gingivalis gingipains to trigger a proinflammatory response in human monocyte-derived macrophages. Both Arg- and Lys-gingipain preparations induced the secretion of TNF-α and IL-8 by macrophages. Stimulation of macrophages with Arg-gingipain A/B preparation at the highest concentration was associated with lower amounts of cytokines detected, a phenomenon likely related to proteolytic degradation. The inflammatory response induced by gingipains was not dependent of their catalytic activity since heat-inactivated preparations were still effective. Stimulating macrophages with gingipain preparations was associated with increased levels of phosphorylated p38α MAPK suggesting its involvement in cell activation. In conclusion, our study brought clear evidence that P. gingivalis Arg- and Lys-gingipains may contribute to the host inflammatory response, a critical factor in periodontitis-associated tissue destruction.
机译:牙龈卟啉单胞菌是慢性牙周炎的主要病原体,可产生多种毒力因子,包括Arg和Lys-gingipain半胱氨酸蛋白酶。在这项研究中,我们调查了牙龈卟啉单胞菌牙龈蛋白酶在人类单核细胞衍生的巨噬细胞中引发促炎反应的能力。 Arg-和Lys-gingipain制剂均诱导巨噬细胞分泌TNF-α和IL-8。用最高浓度的Arg-gingipain A / B制剂刺激巨噬细胞与检测到的细胞因子含量降低有关,这种现象很可能与蛋白水解降解有关。由于热灭活的制剂仍然有效,因此由姜黄素诱导的炎性反应并不取决于其催化活性。姜黄素制剂刺激巨噬细胞与磷酸化的p38αMAPK水平升高有关,表明其参与细胞活化。总之,我们的研究提供了明确的证据,牙龈卟啉单胞菌的Arg和Lys-gingipains可能有助于宿主炎症反应,这是牙周炎相关组织破坏的关键因素。

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