...
首页> 外文期刊>Molecular Immunology >Isoflavone-rich extracts from wooly glycine Glycine tomentella inhibits LPS-induced TNF-alpha expression in a macrophage cell line of Atlantic salmon (Salmo salar L.).
【24h】

Isoflavone-rich extracts from wooly glycine Glycine tomentella inhibits LPS-induced TNF-alpha expression in a macrophage cell line of Atlantic salmon (Salmo salar L.).

机译:羊毛甘氨酸甘蓝小肠中富含异黄酮的提取物可抑制大西洋鲑(Salmo salar L.)巨噬细胞细胞系中LPS诱导的TNF-α表达。

获取原文
获取原文并翻译 | 示例

摘要

The immunomodulatory effects of an isoflavone-rich extract from the root of wooly glycine Glycine tomentella (GTE) were studied in a macrophage-like cell line from Atlantic salmon (TO cells). The TO cell line was stimulated with defined concentrations of lipopolysaccharide (LPS) from Escherichia coli (serotype O127:B8) for defined time periods to induce expression of pro-inflammatory enzymes and cytokines. Cyclooxygenase-2 (COX-2), 5-lipoxygenase (5-LOX), tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) were measured by real-time PCR methods and combined with analyses of eicosanoid production in cell extracts and evaluation of molecules of the TNF-alpha cell signaling pathway. The results showed that TNF-alpha was strongly induced by LPS, while GTE (25miicrog/ml) inhibited 67% of the TNF-alpha response when added to the cells together with LPS. Incubation of LPS in combination of GTE in TO cells caused increased intracellular prostaglandin E2 (PGE2), and reduced activation of p38 MAP kinase compared to LPS alone. GTE seemed to arrest NADPH oxidation, the coenzyme for carbonyl reductase and the prostaglandin-E2 9-reductase converting PGE2 to PGF2. We suggest that the mechanism of increased intracellular PGE2 levels following GTE treatment is caused by reduced breakdown of PGE2. GTE did not inhibit the other pro-inflammatory responses in LPS stimulated cells studied herein. IL-1beta and COX-2 showed moderately increased levels of expression likely caused by the increased PGE2.
机译:在来自大西洋鲑鱼(TO细胞)的巨噬细胞样细胞系中研究了羊毛甘氨酸甘氨酸肠绒毛虫(GTE)根部富含异黄酮提取物的免疫调节作用。用限定浓度的大肠杆菌脂多糖(LPS)(O127:B8型)刺激TO细胞系一段确定的时间,以诱导促炎性酶和细胞因子的表达。通过实时PCR方法测量环氧合酶2(COX-2),5-脂氧合酶(5-LOX),肿瘤坏死因子-α(TNF-alpha)和白介素-1β(IL-1beta),并与细胞提取物中类花生酸的产生以及TNF-α细胞信号通路分子的评估。结果表明,LPS强烈诱导TNF-α,而LTE与LPS一起加入细胞时,GTE(25miicrog / ml)抑制了67%的TNF-α反应。与单独的LPS相比,将LPS与GTE结合在TO细胞中进行孵育会导致细胞内前列腺素E2(PGE2)升高,并降低p38 MAP激酶的激活。 GTE似乎阻止了NADPH的氧化,羰基还原酶的辅酶和将PGE2转化为PGF2的前列腺素E2 9-还原酶。我们建议,GTE治疗后细胞内PGE2水平升高的机制是由PGE2分解减少引起的。 GTE在本文研究的LPS刺激的细胞中不抑制其他促炎反应。 IL-1beta和COX-2显示中等程度的表达水平升高,可能是由PGE2升高引起的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号