首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Niflumic acid and MSI-2216 reduce TNF-alpha-induced mucin expression in human airway mucosa.
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Niflumic acid and MSI-2216 reduce TNF-alpha-induced mucin expression in human airway mucosa.

机译:尼氟酸和MSI-2216降低人气道粘膜中TNF-α诱导的粘蛋白表达。

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BACKGROUND: Human chloride channel, calcium-activated 1 (hCLCA1) has been shown to induce mucin (MUC) gene expression and mucus production in bronchial epithelial cells. Objective To investigate whether blocking hCLCA1 decreases mucus production. METHODS: Expression of hCLCA1 and mucus was stimulated with TNF-alpha in human upper airway mucosal explant tissue. MUC5AC mRNA and mucus protein expression was blocked by inhibiting hCLCA1 by using channel blockers (niflumic acid [NFA] and MSI-2216) without and with TNF-alpha stimulation. Expression of MUC5AC, hCLCA1, and COX-2 mRNA was quantified by using real-time PCR. Mucus protein was assessed by periodic acid Schiff staining. Laser capture microdissection was performed to quantify hCLCA1 and MUC5AC mRNA expression in epithelial cells derived from mucosal explant tissue. RESULTS: TNF-alpha significantly increased MUC5AC and hCLCA1 mRNA as well as mucus and hCLCA1 protein expression in the mucosal explant tissue ( P < .05). Inhibition of hCLCA1 with NFA orMSI-2216 showed a significant dose-dependent reduction of mucus production for both blockers in the mucosal explant tissue ( P < .05). MUC5AC mRNA was also decreased by both blockers in the whole mucosal tissue and in laser-captured mucosa epithelial cells. CONCLUSIONS: Unstimulated and TNF-alpha-induced mucin expression could be decreased by NFA and MSI-2216. Inhibiting hCLCA1 may be a potential new approach to reduce mucus overproduction.
机译:背景:人类氯化物通道钙激活1(hCLCA1)已显示在支气管上皮细胞中诱导粘蛋白(MUC)基因表达和粘液产生。目的探讨阻断hCLCA1是否降低粘液产生。方法:TNF-α刺激人上呼吸道黏膜外植体组织中hCLCA1和黏液的表达。在不使用TNF-α刺激和不使用TNF-α刺激的情况下,通过使用通道阻断剂(尼氟酸[NFA]和MSI-2216)抑制hCLCA1可以阻断MUC5AC mRNA和粘液蛋白的表达。通过使用实时PCR定量MUC5AC,hCLCA1和COX-2 mRNA的表达。通过高碘酸希夫(Schiff)染色评估粘液蛋白。进行激光捕获显微切割术以定量来源于粘膜外植体组织的上皮细胞中的hCLCA1和MUC5AC mRNA表达。结果:TNF-α显着增加了黏膜外植体组织中MUC5AC和hCLCA1 mRNA的表达以及黏液和hCLCA1蛋白的表达(P <0.05)。 NFA或MSI-2216对hCLCA1的抑制作用表明粘膜外植体组织中两种阻滞剂的粘液产生均显着剂量依赖性降低(P <.05)。在整个粘膜组织和激光捕获的粘膜上皮细胞中,两种阻滞剂均可降低MUC5AC mRNA的表达。结论:NFA和MSI-2216可以减少未刺激的和TNF-α诱导的粘蛋白表达。抑制hCLCA1可能是减少粘液过量产生的潜在新方法。

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