【2h】

Adenine attenuates lipopolysaccharide-induced inflammatory reactions

机译:腺嘌呤减弱脂多糖诱导的炎症反应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A nucleobase adenine is a fundamental component of nucleic acids and adenine nucleotides. Various biological roles of adenine have been discovered. It is not produced from degradation of adenine nucleotides in mammals but produced mainly during polyamine synthesis by dividing cells. Anti-inflammatory roles of adenine have been supported in IgE-mediated allergic reactions, immunological functions of lymphocytes and dextran sodium sulfate-induced colitis. However adenine effects on Toll-like receptor 4 (TLR4)-mediated inflammation by lipopolysaccharide (LPS), a cell wall component of Gram negative bacteria, is not examined. Here we investigated anti-inflammatory roles of adenine in LPS-stimulated immune cells, including a macrophage cell line RAW264.7 and bone marrow derived mast cells (BMMCs) and peritoneal cells in mice. In RAW264.7 cells stimulated with LPS, adenine inhibited production of pro-inflammatory cytokines TNF-α and IL-6 and inflammatory lipid mediators, prostaglandin E2 and leukotriene B4. Adenine impeded signaling pathways eliciting production of these inflammatory mediators. It suppressed IκB phosphorylation, nuclear translocation of nuclear factor κB (NF-κB), phosphorylation of Akt and mitogen activated protein kinases (MAPKs) JNK and ERK. Although adenine raised cellular AMP which could activate AMP-dependent protein kinase (AMPK), the enzyme activity was not enhanced. In BMMCs, adenine inhibited the LPS-induced production of TNF-α, IL-6 and IL-13 and also hindered phosphorylation of NF-κB and Akt. In peritoneal cavity, adenine suppressed the LPS-induced production of TNF-α and IL-6 by peritoneal cells in mice. These results show that adenine attenuates the LPS-induced inflammatory reactions.
机译:核碱基腺嘌呤是核酸和腺嘌呤核苷酸的基本成分。已经发现腺嘌呤的各种生物学作用。它不是由哺乳动物腺嘌呤核苷酸的降解产生的,而是主要在多胺合成过程中通过分裂细胞产生的。在IgE介导的过敏反应,淋巴细胞的免疫功能和右旋糖酐硫酸钠诱发的结肠炎中已支持了腺嘌呤的抗炎作用。但是,未检查腺嘌呤对脂多糖(LPS)(革兰氏阴性细菌的细胞壁成分)对Toll样受体4(TLR4)介导的炎症的影响。在这里,我们研究了腺嘌呤在LPS刺激的免疫细胞(包括巨噬细胞系RAW264.7和骨髓衍生的肥大细胞(BMMC)和小鼠的腹膜细胞)中的抗炎作用。在LPS刺激的RAW264.7细胞中,腺嘌呤抑制促炎性细胞因子TNF-α和IL-6以及炎性脂质介质,前列腺素E2和白三烯B4的产生。腺嘌呤阻碍了引起这些炎性介质产生的信号传导途径。它抑制了IκB磷酸化,核因子κB(NF-κB)的核易位,Akt和有丝分裂原激活的蛋白激酶(MAPK)JNK和ERK的磷酸化。尽管腺嘌呤提高了可以激活AMP依赖性蛋白激酶(AMPK)的细胞AMP,但酶的活性并未增强。在BMMC中,腺嘌呤抑制LPS诱导的TNF-α,IL-6和IL-13的产生,并阻碍NF-κB和Akt的磷酸化。在腹腔中,腺嘌呤抑制小鼠腹膜细胞LPS诱导的TNF-α和IL-6产生。这些结果表明腺嘌呤减弱了LPS诱导的炎症反应。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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