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葡萄籽原花青素提取物通过 MAPK 通路抑制人肺上皮细胞中白细胞介素-17 诱导的白细胞介素-6 产生。

Grape seed proanthocyanidin extract inhibits interleukin-17-induced interleukin-6 production via MAPK pathway in human pulmonary epithelial cells.

机构信息

Department of Biochemistry, Pain Research Center, School of Medicine, Keimyung University, Daegu 704-701, Republic of Korea.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2011 Jun;383(6):555-62. doi: 10.1007/s00210-011-0633-y. Epub 2011 Apr 12.

Abstract

This study was aimed to investigate the effect of grape seed proanthocyanidin extract (GSPE) on interleukin-17 (IL-17)-induced interleukin-6 (IL-6) production in A549 human pulmonary epithelial cells. Cells were treated with IL-17 (10 ng/ml) or GSPE (50 μg/ml), or both. The effects of GSPE on cell viability and apoptosis were evaluated. The mRNA and protein levels of IL-6 were determined by reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Expressions of inhibitory factor κB-α (IκB-α) and ERK 1/2, p38, and JNK mitogen-activated protein kinase (MAPK) were examined by Western blot analysis. GSPE significantly inhibited both GSPE treatment only and IL-17-induced mRNA expressions and protein productions of IL-6 in pulmonary epithelial cells (p < 0.01). GSPE decreased the IL-17-induced phosphorylation of IκB-α. The IL-17 stimulated ERK 1/2, p38, and JNK MAPK activities and GSPE decreased IL-17-stimulated ERK 1/2, p38, and JNK MAPK activities. GSPE also attenuated TNF-α and IL-1β-induced IL-6 productions (p < 0.05). Our results show that GSPE may inhibit IL-17-stimulated IL-6 productions in human pulmonary epithelial cells by inhibiting MAPK and nuclear factor-κB-mediated signaling pathway.

摘要

本研究旨在探讨葡萄籽原花青素提取物(GSPE)对 A549 人肺上皮细胞中白细胞介素-17(IL-17)诱导的白细胞介素-6(IL-6)产生的影响。用 IL-17(10ng/ml)或 GSPE(50μg/ml)或两者处理细胞。评估 GSPE 对细胞活力和细胞凋亡的影响。通过逆转录聚合酶链反应和酶联免疫吸附测定分别测定 IL-6 的 mRNA 和蛋白水平。通过 Western blot 分析检测抑制因子 κB-α(IκB-α)和 ERK 1/2、p38 和 JNK 丝裂原激活蛋白激酶(MAPK)的表达。GSPE 显著抑制了 GSPE 处理和 IL-17 诱导的肺上皮细胞中 IL-6 的 mRNA 表达和蛋白产生(p<0.01)。GSPE 降低了 IL-17 诱导的 IκB-α磷酸化。IL-17 刺激 ERK 1/2、p38 和 JNK MAPK 活性,GSPE 降低了 IL-17 刺激的 ERK 1/2、p38 和 JNK MAPK 活性。GSPE 还减弱了 TNF-α和 IL-1β诱导的 IL-6 产生(p<0.05)。我们的结果表明,GSPE 可能通过抑制 MAPK 和核因子-κB 介导的信号通路抑制 IL-17 刺激的人肺上皮细胞中 IL-6 的产生。

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