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钝叶决明子种子中分离得到的钝叶苏木酚通过影响 NF-κB 通路调节气道上皮细胞的 MUC5AC 粘蛋白基因表达和产生。

Obtusifolin isolated from the seeds of Cassia obtusifolia regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via affecting NF-κB pathway.

机构信息

Department of Pharmacology, School of Medicine, Chungnam National University, Daejeon, Korea.

Department of Food Science and Nutrition, Pukyong National University, Busan, Korea.

出版信息

Phytother Res. 2019 Apr;33(4):919-928. doi: 10.1002/ptr.6284. Epub 2019 Jan 10.

DOI:10.1002/ptr.6284
PMID:30632219
Abstract

We investigated whether obtusin, obtusifolin, and cassiaside isolated from the seeds of Cassia obtusifolia inhibit the gene expression and production of airway mucin 5AC (MUC5AC). Confluent NCI-H292 cells were pretreated with obtusin, obtusifolin, or cassiaside for 30 min and then stimulated with epidermal growth factor (EGF), phorbol 12-myristate 13-acetate (PMA), or tumor necrosis factor-α (TNF-α) for 24 hr. The MUC5AC mucin gene expression was measured by reverse transcription-polymerase chain reaction. Production of MUC5AC mucin protein was measured by enzyme-linked immunosorbent assay. To elucidate the action mechanism of obtusifolin, effect of obtusifolin on PMA-induced nuclear factor kappa B (NF-κB) signaling pathway was investigated by western blot analysis. Obtusin, obtusifolin, or cassiaside inhibited the expression of MUC5AC mucin gene and the production of MUC5AC mucin protein, induced by EGF, PMA, or TNF-α. Obtusifolin inhibited PMA-induced activation (phosphorylation) of inhibitory kappa B kinase, and thus phosphorylation and degradation of inhibitory kappa B alpha. Obtusifolin inhibited PMA-induced nuclear translocation of NF-κB p65. These results suggest that obtusifolin can regulate the production and gene expression of mucin by acting on airway epithelial cells through regulation of NF-κB signaling pathway.

摘要

我们研究了从决明子种子中分离得到的钝叶决明素、钝叶决明苷和决明子苷是否能抑制气道粘蛋白 5AC(MUC5AC)的基因表达和产生。将汇合的 NCI-H292 细胞用钝叶决明素、钝叶决明苷或决明子苷预处理 30min,然后用表皮生长因子(EGF)、佛波醇 12-肉豆蔻酸 13-乙酸酯(PMA)或肿瘤坏死因子-α(TNF-α)刺激 24hr。通过逆转录-聚合酶链反应测定 MUC5AC 粘蛋白基因的表达。通过酶联免疫吸附试验测定 MUC5AC 粘蛋白的产生。为了阐明钝叶决明苷的作用机制,通过 Western blot 分析研究了钝叶决明苷对 PMA 诱导的核因子 kappa B(NF-κB)信号通路的影响。钝叶决明素、钝叶决明苷或决明子苷抑制 EGF、PMA 或 TNF-α诱导的 MUC5AC 粘蛋白基因表达和 MUC5AC 粘蛋白的产生。钝叶决明苷抑制 PMA 诱导的抑制性 κB 激酶的激活(磷酸化),从而抑制抑制性 κBα的磷酸化和降解。钝叶决明苷抑制 PMA 诱导的 NF-κB p65 核易位。这些结果表明,钝叶决明苷可以通过调节 NF-κB 信号通路,作用于气道上皮细胞来调节粘蛋白的产生和基因表达。

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