Hyperoside Regulates the Level of Thymic Stromal Lymphopoietin through Intracellular Calcium Signalling

被引:14
作者
Han, Na-Ra [1 ]
Go, Ji-Hyun [1 ]
Kim, Hyung-Min [1 ]
Jeong, Hyun-Ja [2 ,3 ]
机构
[1] Kyung Hee Univ, Coll Korean Med, Dept Pharmacol, Seoul 130701, South Korea
[2] Hoseo Univ, Inflammatory Dis Res Ctr, Asan 336795, Chungnam, South Korea
[3] Hoseo Univ, Biochip Res Ctr, Asan 336795, Chungnam, South Korea
基金
新加坡国家研究基金会;
关键词
hyperoside; thymic stromal lymphopoietin; mast cell; intracellular calcium; caspase-1; NF-KAPPA-B; CRATAEGUS-PINNATIFIDA; RECEPTOR; PATHWAY; INHIBITION; ACTIVATION; CASPASE; PROTEIN; MODULATION; EXPRESSION;
D O I
10.1002/ptr.5099
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Hyperoside (HYP) is the principle active component of Crataegus pinnatifida. Thymic stromal lymphopoietin (TSLP) plays a vital role in the pathogenesis of allergic reactions. Here, we investigated how HYP regulates the levels of TSLP in a human mast cell line, HMC-1 cells. We analyzed the levels of TSLP by treatment with HYP in phorbolmyristate acetate plus calciumionophoreA23187-stimulatedHMC-1 cells with ELISA and a polymerase chain reaction analysis. We also analyzed the pathway that HYP regulates TSLP by measuring the level of fluorescent intracellular calcium and using a Western blot analysis. HYP decreased the level of intracellular calciumin stimulated HMC-1 cells. It also significantly decreased the production and mRNA expression of TSLP in stimulated HMC-1 cells. It significantly decreased the levels of receptor-interacting protein 2 and active caspase-1 in stimulated HMC-1 cells. HYP significantly decreased the translocation of NF-kappa B into the nucleus and degradation of I kappa B alpha in the cytoplasm in stimulated HMC-1 cells. Furthermore, it significantly decreased the production and mRNA expression of interleukin-1 beta and interleukin-6 in stimulated HMC-1 cells. Taken together, our findings establish HYP as a potential agent for the treatment of allergic reactions. Copyright (C) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1077 / 1081
页数:5
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