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Interleukin-18 and Gamma Interferon Production by Oral Epithelial Cells in Response to Exposure to Candida albicans or Lipopolysaccharide Stimulation

机译:暴露于白色念珠菌或脂多糖刺激下口腔上皮细胞产生白介素-18和γ干扰素

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摘要

Oral candidiasis is a collective name for a group of disorders caused by the dimorphic fungus Candida albicans. Host defenses against C. albicans essentially fall into two categories: specific immune mechanisms and local oral mucosal epithelial cell defenses. Since oral epithelial cells secrete a variety of cytokines and chemokines in response to oral microorganisms and since C. albicans is closely associated with oral epithelial cells as a commensal organism, we wanted to determine whether interleukin-18 (IL-18) and gamma interferon (IFN-γ) were produced by oral epithelial cells in response to C. albicans infection and lipopolysaccharide (LPS) stimulation. Our results showed that IL-18 mRNA and protein were constitutively expressed by oral epithelial cells and were down-regulated by Candida infections but increased following LPS stimulation. Both C. albicans and LPS significantly decreased pro-IL-18 (24 kDa) levels and increased active IL-18 (18 kDa) levels. This effect was IL-1β-converting-enzyme dependent. The increase in active IL-18 protein levels promoted the production of IFN-γ by infected cells. No effect was obtained with LPS. Although produced only at an early stage, secreted IFN-γ seemed to be a preferential response by oral epithelial cells to C. albicans growth. These results provide additional evidence for the contribution of oral epithelial cells to local (direct contact) and systemic (IL-18 and IFN-γ production) defense against exogenous stimulation such as C. albicans infection or LPS stimulation.
机译:口腔念珠菌病是由双形真菌白色念珠菌引起的一组疾病的统称。针对白色念珠菌的宿主防御基本上分为两类:特定的免疫机制和局部口腔粘膜上皮细胞防御。由于口腔上皮细胞会响应口腔微生物而分泌多种细胞因子和趋化因子,并且白色念珠菌与口腔上皮细胞作为共生生物密切相关,因此我们想确定白介素-18(IL-18)和γ干扰素(口服上皮细胞响应白色念珠菌感染和脂多糖(LPS)刺激而产生IFN-γ)。我们的结果表明,IL-18 mRNA和蛋白在口腔上皮细胞中组成性表达,并被念珠菌感染下调,但在LPS刺激后增加。白色念珠菌和LPS均显着降低了IL-18的原水平(24 kDa),并增加了活性IL-18(18 kDa)的水平。该作用是IL-1β转化酶依赖性的。活性IL-18蛋白水平的提高促进了被感染细胞产生IFN-γ。 LPS无效。尽管分泌的IFN-γ仅在早期产生,但似乎是口腔上皮细胞对白色念珠菌生长的优先反应。这些结果为口腔上皮细胞在抵抗外源性刺激(例如白色念珠菌感染或LPS刺激)的局部(直接接触)和全身性(IL-18和IFN-γ产生)防御中的贡献提供了补充证据。

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