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首页> 外文期刊>European journal of oral sciences >Antimicrobial activity and regulation of CXCL9 and CXCL10 in oral keratinocytes
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Antimicrobial activity and regulation of CXCL9 and CXCL10 in oral keratinocytes

机译:口腔角质形成细胞的抗菌活性及CXCL9和CXCL10的调控

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摘要

Chemokine (C-X-C motif) ligand (CXCL)9 and CXCL10 are dysregulated in oral inflammatory conditions, and it is not known if these chemokines target microorganisms that form oral biofilm. The aim of this study was to investigate the antimicrobial activity of CXCL9 and CXCL10 on oral microflora and their expression profiles in oral keratinocytes following exposure to inflammatory and infectious stimuli. Streptococcus sanguinis was used as a model and Escherichia coli as a positive control. The antimicrobial effect of CXCL9/CXCL10 was tested using a radial diffusion assay. mRNA transcripts were isolated from lipopolysaccharide (LPS)-treated and untreated (control) oral keratinocyte cell lines at 2-, 4-, 6-, and 8-h time-points of culture. The CXCL9/10 expression profile in the presence or absence of interferon- (IFN-) was assessed using semiquantitative PCR. Although both chemokines demonstrated antimicrobial activity, CXCL9 was the most effective chemokine against both S. sanguinis and E coli. mRNA for CXCL10 was expressed in control cells and its production was enhanced at all time-points following stimulation with LPS. Conversely, CXCL9 mRNA was not expressed in control or LPS-stimulated cells. Finally, stimulation with IFN- enhanced basal expression of both CXCL9 and CXCL10 in oral keratinocytes. Chemokines derived from oral epithelium, particularly CXCL9, demonstrate antimicrobial properties. Bacterial and inflammatory-stimulated up-regulation of CXCL9/10 could represent a key element in oral bacterial colonization homeostasis and host-defense mechanisms.
机译:趋化因子(C-X-C基序)配体(CXCL)9和CXCL10在口腔炎症条件下失调,尚不知道这些趋化因子是否靶向形成口腔生物膜的微生物。这项研究的目的是调查暴露于炎症和感染性刺激后,CXCL9和CXCL10对口腔菌群的抗菌活性及其在口腔角质形成细胞中的表达谱。血链球菌用作模型,大肠杆菌用作阳性对照。使用径向扩散测定法测试了CXCL9 / CXCL10的抗菌作用。在培养的2、4、6、8小时时间点,从脂多糖(LPS)处理和未处理(对照)的口腔角质形成细胞系中分离出mRNA转录本。使用半定量PCR评估存在或不存在干扰素-(IFN-)时的CXCL9 / 10表达谱。尽管两种趋化因子均具有抗微生物活性,但CXCL9是针对血红链霉菌和大肠杆菌的最有效趋化因子。 CXCL10的mRNA在对照细胞中表达,并在LPS刺激后的所有时间点均提高了产量。相反,CXCL9 mRNA在对照或LPS刺激的细胞中不表达。最后,在角质形成细胞中用IFN刺激增强了CXCL9和CXCL10的基础表达。源自口腔上皮的趋化因子,特别是CXCL9,表现出抗菌特性。细菌和炎症刺激的CXCL9 / 10上调可能代表了口腔细菌定植稳态和宿主防御机制的关键因素。

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