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Infection of microglia with Porphyromonas gingivalis promotes cell migration and an inflammatory response through the gingipain-mediated activation of protease-activated receptor-2 in mice

机译:小胶质细胞感染牙龈卟啉单胞菌可促进细胞迁移并通过牙龈蛋白酶介导的蛋白酶激活受体2激活小鼠炎症反应

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摘要

Despite a clear correlation between periodontitis and cognitive decline in Alzheimer’s disease, the precise mechanism underlying the relationship remains unclear. The periodontal pathogen Porphyromonas gingivalis produces a unique class of cysteine proteinases termed gingipains that comprises Arg-gingipain (Rgp) and Lys-gingipain (Kgp). Rgp and Kgp are important in the bacterial mediated host cell responses and the subsequent intracellular signaling in infected cells. In the present study, we attempted to clarify the potential effects of Rgp and Kgp on the cellular activation of brain-resident microglia. We provide the first evidence that Rgp and Kgp cooperatively contribute to the P. gingivalis-induced cell migration and expression of proinflammatory mediators through the activation of protease-activated receptor 2. The subsequent activation of phosphoinositide 3-kinase/Akt and mitogen-activated protein kinase/extracellular signal-regulated kinase (ERK) kinase/ERK pathways contributes to cell migration and inflammatory response of microglia.
机译:尽管牙周炎和阿尔茨海默氏病的认知能力下降之间存在明显的相关性,但这种关系的确切机制仍不清楚。牙周病原体牙龈卟啉单胞菌可产生一类独特的半胱氨酸蛋白酶,称为半胱氨酸蛋白酶,其中包含Arg-gingipain(Rgp)和Lys-gingipain(Kgp)。 Rgp和Kgp在细菌介导的宿主细胞反应以及随后被感染细胞的细胞内信号传导中很重要。在本研究中,我们试图阐明Rgp和Kgp对大脑驻留小胶质细胞激活的潜在影响。我们提供了第一个证据,即Rgp和Kgp通过蛋白酶激活受体2的激活共同促进牙龈卟啉单胞菌诱导的细胞迁移和促炎性介质的表达。随后磷酸肌醇3-激酶/ Akt和促分裂原激活蛋白的激活激酶/细胞外信号调节激酶(ERK)激酶/ ERK通路有助于细胞迁移和小胶质细胞的炎症反应。

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