首页> 美国卫生研究院文献>Clinical and Developmental Immunology >Immunobiotics Beneficially Modulate TLR4 Signaling Triggered by Lipopolysaccharide and Reduce Hepatic Steatosis In Vitro
【2h】

Immunobiotics Beneficially Modulate TLR4 Signaling Triggered by Lipopolysaccharide and Reduce Hepatic Steatosis In Vitro

机译:免疫抗生素有益地调节脂多糖触发的TLR4信号传导并减少肝脂肪变性

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

Hepatic inflammation and injury may result from the translocation of pathological bacteria and their proinflammatory mediators. Probiotics attenuate hepatic diseases related to inflammation by exhibiting immunoregulatory effects. Therefore, this study was conducted to evaluate lipid reduction and immunoregulatory potentials of probiotic bacteria in vitro. HepG2 cells treated with total cellular fluid (TCF) of LABs reduced lipid accumulation. Moreover, cells responded to lipopolysaccharide (LPS) by producing higher levels of IL-6, IL-8, MCP-1, and TNF-α. TCF of LABs treatment showed remarkably diminished levels of the expression of these cytokines via modulation of the expression of TLR-negative regulators, as well as MAPK and NF-κB pathways. Moreover, heat-killed LABs were able to diminish TGF-β, IL-1β, and IL-6 and to increase IL-10 and TLR4 levels in THP-1 cells. LABs also decreased the protein level of TNF-α. These results demonstrated that immunobiotics exhibit potent immunoregulatory activity and may be used as effective therapeutic agents to alleviate inflammatory response.
机译:病理性细菌及其促炎介质易位,可能导致肝脏发炎和损伤。益生菌通过发挥免疫调节作用来减轻与炎症有关的肝病。因此,本研究旨在评估体外益生菌的脂质减少和免疫调节潜力。用LAB的总细胞液(TCF)处理的HepG2细胞减少了脂质积聚。此外,细胞通过产生更高水平的IL-6,IL-8,MCP-1和TNF-α对脂多糖(LPS)作出反应。 LABs处理的TCF显示,通过调节TLR阴性调节子的表达以及MAPK和NF-κB途径,这些细胞因子的表达水平显着降低。此外,热杀死的LAB能够减少THP-1细胞中的TGF-β,IL-1β和IL-6并增加IL-10和TLR4的水平。 LABs也降低了TNF-α的蛋白水平。这些结果证明,免疫生物素表现出有效的免疫调节活性,并且可以用作减轻炎症反应的有效治疗剂。

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