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Hop 水提物抑制人鼻上皮细胞中双链 RNA 诱导的胸腺基质淋巴细胞生成素释放。

Hop water extract inhibits double-stranded RNA-induced thymic stromal lymphopoietin release from human nasal epithelial cells.

机构信息

Frontier Laboratories of Value Creation, Sapporo Breweries, Ltd., Shizuoka, Japan.

出版信息

Am J Rhinol Allergy. 2012 Nov-Dec;26(6):433-8. doi: 10.2500/ajra.2012.26.3814.

Abstract

BACKGROUND

Thymic stromal lymphopoietin (TSLP) acts as a master switch for allergic inflammation and plays a key role in allergic diseases, including allergic rhinitis. Double-stranded RNA (dsRNA) recognized by Toll-like receptor 3 (TLR3) strongly activates TSLP release from human nasal epithelial cells (HNECs). Hop (Humulus lupulus L.) extracts have been shown to have potent pharmacologic effects on inflammation.

METHODS

To investigate whether a hop water extract (HWE) prevents TSLP release from HNECs, human telomerase reverse transcriptase (hTERT)-transfected HNECs, used as a model of normal HNECs, were pretreated with HWE before treatment with the TLR3 ligand Polyinosine-polycytidylic acid (poly[I:C]).

RESULTS

In the hTERT-transfected HNECs, treatment with HWE significantly reduced poly(I:C)-induced production and release of TSLP in a dose-dependent manner, as well as dexamethasone. Treatment with the protein kinase C (PKC) inhibitor GF109203X and NF-κB inhibitor IMD-0354 also reduced poly(I:C)-induced TSLP release from hTERT-transfected HNECs. Treatment with HWE efficiently prevented up-regulation of PKC activity by 12-O-tetradecanoyl phorbol-13-acetate but not NF-κB activity induced by IL-1β in hTERT-transfected HNECs.

CONCLUSION

Our results clearly indicated that HWE inhibited dsRNA-induced production and release of TSLP via a PKC signal pathway in HNECs and it may have potent preventive effects against allergic rhinitis.

摘要

背景

胸腺基质淋巴细胞生成素 (TSLP) 作为过敏炎症的主开关,在包括过敏性鼻炎在内的过敏疾病中发挥关键作用。Toll 样受体 3 (TLR3) 识别的双链 RNA (dsRNA) 可强烈激活人鼻上皮细胞 (HNEC) 中 TSLP 的释放。啤酒花 (Humulus lupulus L.) 提取物已被证明对炎症具有强大的药理作用。

方法

为了研究啤酒花水煎剂 (HWE) 是否可防止 HNEC 中 TSLP 的释放,我们使用人端粒酶逆转录酶 (hTERT) 转染的 HNEC 作为正常 HNEC 的模型,在 TLR3 配体聚肌苷酸-聚胞苷酸 (poly[I:C]) 处理前用 HWE 预处理。

结果

在 hTERT 转染的 HNEC 中,HWE 以剂量依赖性方式显著降低 poly(I:C)诱导的 TSLP 的产生和释放,其作用与地塞米松相当。蛋白激酶 C (PKC) 抑制剂 GF109203X 和 NF-κB 抑制剂 IMD-0354 处理也降低了 hTERT 转染的 HNEC 中 poly(I:C)诱导的 TSLP 释放。HWE 处理可有效防止 12-O-十四烷酰佛波醇-13-乙酸酯诱导的 PKC 活性上调,但不能防止 IL-1β诱导的 hTERT 转染的 HNEC 中 NF-κB 活性上调。

结论

我们的结果清楚地表明,HWE 通过 PKC 信号通路抑制 dsRNA 诱导的 HNEC 中 TSLP 的产生和释放,它可能对过敏性鼻炎具有潜在的预防作用。

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