Department of Oral Microbiology & Immunology, Dental Research Institute, and BK21 Program, School of Dentistry, Seoul National University, Seoul 110-749, Republic of Korea.
J Ethnopharmacol. 2010 Jan 8;127(1):55-61. doi: 10.1016/j.jep.2009.09.051. Epub 2009 Sep 30.
In order to elucidate immunoregulatory mechanisms of Cordyceps militaris, a methanol extract of Cordyceps militaris grown on germinated soybeans was prepared and its immunoregulatory effect in the human lung epithelial cells was investigated by examining its ability to induce IL-8 expression.
Cordyceps militaris grown on germinated soybeans was extracted with 80% methanol (GSC4M) and used for stimulation of a human lung epithelial cell-line, A549. An enzyme-linked immunosorbent assay and reverse transcription-polymerase chain reaction were performed to examine the production of IL-8 protein and its mRNA, respectively. For the analysis of transcription factors regulating IL-8 transcriptional activation, the nuclear fraction was extracted from GSC4M-treated A549 cells and subjected to electrophoretic mobility shift assay.
GSC4M induced IL-8 protein secretion and its mRNA expression from A549 cells in a dose- and time-dependent manner. GSC4M-induced IL-8 expression was inhibited by an inhibitor for lipid rafts formation but not by that for clathrin-coated pits. In addition, signaling pathways for GSC4M-induced IL-8 expression were mediated through ERK and JNK but hardly through p38 kinase. Furthermore, GSC4M augmented the DNA-binding activity of the transcription factors AP-1, NF-IL6, and NF-kappaB, all of which are involved in the transcriptional activation of the IL-8 gene.
Cordyceps militaris grown on germinated soybeans stimulates lung epithelial cells to produce IL-8 through lipid rafts formation and signaling pathways via ERK and JNK.
为了阐明蛹虫草的免疫调节机制,本研究采用发芽大豆培养的蛹虫草甲醇提取物,通过检测其诱导白细胞介素-8(IL-8)表达的能力,研究其在人肺上皮细胞中的免疫调节作用。
采用 80%甲醇(GSC4M)提取发芽大豆培养的蛹虫草,用于刺激人肺上皮细胞系 A549。采用酶联免疫吸附试验和逆转录-聚合酶链反应分别检测 IL-8 蛋白和其 mRNA 的产生。为了分析调节 IL-8 转录激活的转录因子,从 GSC4M 处理的 A549 细胞中提取核部分,并进行电泳迁移率变动分析。
GSC4M 以剂量和时间依赖的方式诱导 A549 细胞分泌 IL-8 蛋白及其 mRNA。GSC4M 诱导的 IL-8 表达可被脂筏形成抑制剂抑制,但不能被网格蛋白包被小凹抑制剂抑制。此外,GSC4M 诱导的 IL-8 表达的信号通路通过 ERK 和 JNK 介导,但几乎不通过 p38 激酶介导。此外,GSC4M 增强了转录因子 AP-1、NF-IL6 和 NF-κB 的 DNA 结合活性,它们均参与 IL-8 基因的转录激活。
发芽大豆培养的蛹虫草通过脂筏形成和 ERK 和 JNK 信号通路刺激肺上皮细胞产生白细胞介素-8。