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Mitogen-activated protein kinases and tumor necrosis factor alpha responses of macrophages infected with Orientia tsutsugamushi

机译:ient虫东方型感染巨噬细胞的丝裂原活化蛋白激酶和肿瘤坏死因子α反应

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摘要

Orientia tsutsugamushi, an obligatory intracellular bacterium, is the causative agent of scrub typhus. The disease is histopathologically characterized by inflammatory manifestations, indicating that orientiae induce mechanisms that amplify the inflammatory response. Here we investigated the transcriptional response of tumor necrosis factor alpha (TNF-l) gene and the host cell responses of nuclear factor-kappa B (NF-B) and mitogen-activated protein kinases (MAPKs) to O. tsutsugamushi. Induction of the TNF-l gene was not blocked by a eukaryotic protein synthesis inhibitor cycloheximide, suggesting that de novo synthesis of host cell protein is not required for this transcriptional response. The induction of TNF-l mRNA by O. tsutsugamushi was not blocked by the inhibitors of NF-B activation. Inactivation of Orientia by heat abolished both MAPK activation and TNF-l production, whereas treatment of host cells with cytochalasin D impaired neither NF-B and MAPK activation nor TNF-l production. In conclusion, our data suggest that O. tsutsugamushi-stimulated TNF-l production and MAPK activation requires cellular attachment by viable orientiae but not bacterial internalization into the host cells.
机译:东方tsu虫(Orientia tsutsugamushi)是一种必需的细胞内细菌,是斑疹伤寒的病原体。该疾病在组织病理学上以炎症表现为特征,表明定向疾病诱导了放大炎症反应的机制。在这里,我们调查了肿瘤坏死因子α(TNF-1)基因的转录反应以及核因子-κB(NF-B)和促分裂原活化蛋白激酶(MAPK)对to虫的宿主细胞反应。真核蛋白质合成抑制剂环己酰亚胺未阻断TNF-1基因的诱导,这表明该转录应答不需要宿主细胞蛋白质的从头合成。 gam虫的诱导TNF-1 mRNA没有被NF-B激活抑制剂所阻断。通过加热使东方的失活消除了MAPK活化和TNF-1产生,而用细胞松弛素D处理宿主细胞既不损害NF-B和MAPK活化也不破坏TNF-1产生。总之,我们的数据表明O虫O. tsutsugamushi刺激的TNF-1产生和MAPK激活需要有活力的定向细胞附着细胞,而不需要细菌内化到宿主细胞中。

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