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Epithelial-mesenchymal transition promotes reactivity of human lung adenocarcinoma A549 cells to CpG ODN

机译:上皮-间质转化促进人肺腺癌A549细胞对CpG ODN的反应性

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Background Epithelial-mesenchymal transition (EMT) is reported to promote airway remodeling in asthmatics, which is the main histological change that causes complex and severe symptoms in asthmatics. However, little is known about whether EMT also plays a role in acute exacerbations of asthma evoked by respiratory tract infections. Methods A human lung adenocarcinoma line, A549, was incubated with TGF-β1 at 10?ng/ml to induce EMT. Then the cells were stimulated with CpG ODN. Expression of surface and intracellular molecules was analyzed by flow cytometry. IL-6, IL-8 and MCP-1 in the culture supernatant were measured by Cytometric Bead Assay, and the expression of mRNA was quantitated by real-time PCR. CpG ODN uptake was analyzed by flow cytometry. Results The culture supernatant levels of IL-6, IL-8 and MCP-1 and the expression of mRNA for these cytokines in CpG ODN-stimulated A549 cells that had undergone EMT was significantly higher compared to those that had not. Addition of ODN H154, a TLR9-inhibiting DNA, significantly suppressed the CpG ODN-induced production of those cytokines. However, flow cytometry found the level of TLR9 expression to be slightly lower in A549 cells that had undergone EMT compared to those that had not. On the other hand, CpG ODN uptake was increased in cells that had undergone EMT. Conclusions EMT induction of A549 cells enhanced CpG ODN uptake and CpG ODN-induced production of IL-6, IL-8 and MCP-1. These results suggest that EMT plays an important role in exacerbation in asthmatics with airway remodeling by enhancing sensitivity to extrinsic pathogens.
机译:背景技术据报道,上皮-间质转化(EMT)可促进哮喘患者的气道重塑,这是导致哮喘患者复杂而严重的症状的主要组织学变化。但是,关于EMT是否在呼吸道感染引起的哮喘急性加重中也起着作用还知之甚少。方法将人肺腺癌细胞系A549与TGF-β1以10?ng / ml的温度孵育以诱导EMT。然后用CpG ODN刺激细胞。通过流式细胞术分析表面和细胞内分子的表达。通过细胞计数珠测定法测定培养上清液中的IL-6,IL-8和MCP-1,并通过实时PCR定量mRNA的表达。通过流式细胞术分析CpG ODN摄取。结果经历过EMT的CpG ODN刺激的A549细胞的培养上清液中IL-6,IL-8和MCP-1的水平以及这些细胞因子的mRNA表达明显高于未经历过EMT的细胞。加入ODN H154(一种抑制TLR9的DNA)可显着抑制CpG ODN诱导的那些细胞因子的产生。然而,流式细胞仪发现,经历过EMT的A549细胞与未经历过EMT的A549细胞相比,TLR9表达水平略低。另一方面,在接受EMT的细胞中CpG ODN的摄取增加了。结论EMT诱导A549细胞增强了CpG ODN的摄取,并增强了CpG ODN诱导的IL-6,IL-8和MCP-1的产生。这些结果表明,EMT通过增强对外部病原体的敏感性,在气道重塑的哮喘发作加重中发挥重要作用。

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