全氟化碳对脂多糖诱导肺泡上皮细胞炎性反应及单免疫球蛋白白介素1相关蛋白表达的影响
DOI:
作者:
作者单位:

作者简介:

通讯作者:

基金项目:

国家自然科学基金(81300050),海军总医院创新培养基金(CXPY201417)


Effects of perfluorocarbon on the inflammatory reaction induced by LPS and the expression of single immunoglobin IL 1 receptor related protein in alveolar epithelial cells
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
    摘要:

    【摘要】 目的 探讨全氟化碳(PFC)对脂多糖(LPS)诱导人肺泡上皮A549细胞炎性反应及单免疫球蛋白白介素1受体相关蛋白(SIGIRR)表达的影响。方法 实验分为正常细胞组、全氟化碳+脂多糖(PFC+LPS)组、全氟化碳(PFC)组及脂多糖(LPS)组。各组细胞经相应处理24 h后,用酶联免疫吸附法(ELISA)检测培养上清中的TNFα、IL6和IL10含量,用蛋白免疫印迹法(Westernblot)检测核转录因子κB (NFκB)和SIGIRR的表达。结果 ELISA结果显示,LPS组TNFα、IL6水平较正常细胞组升高(P<005);PFC+LPS组TNFα、IL6水平较LPS组下降(P<005);与正常细胞组相比,PFC组IL10水平升高(P<005),PFC+LPS组IL10水平较LPS组升高(P<005)。Westernblot 结果显示,与正常细胞组相比,LPS组核内磷酸化NFκB p65表达上调(P<005),PFC+LPS组核内磷酸化NFκB p65表达水平较LPS组降低(P<005);与正常细胞组相比,LPS组SIGIRR表达水平下调(P<005),PFC+LPS组SIGIRR表达水平较LPS组上调(P<005)。PFC本身对TNFα、IL6含量及NFκB p65表达无影响,但PFC可促进A549细胞释放IL10及上调SIGIRR表达(P<005)。结论 PFC可减轻A549细胞对LPS诱导的炎性反应,促进抗炎因子IL10分泌及上调负调控分子SIGIRR表达是可能的分子机制。

    Abstract:

    【Abstract】 Objective To investigate the Effects of perfluorocarbon on the inflammatory reaction induced by LPS and the expression of single immunoglobin IL1 receptor related protein (SIGIRR) in alveolar epithelial cells (A549 cells). Methods The A549 cells were divided into four groups (normal cell group, PFC+LPS group, PFC group and LPS group). A549 cells of each group were incubated for 24 h, and then the culture supernatants, cellular total protein and cellular nuclear protein were collected. The levels of TNFα, IL6 and IL10 in the culture supernatants were detected by ELISA. The protein expression levels of NFκB p65 in nuclear extracts and the protein expression levels of SIGIRR in A549 cells of each group were also measured by Westernblot analysis. Results The results of ELISA demonstrated that the levels of TNFα and IL6 in LPS group were higher than those in normal cell group (P<005). Compared with LPS group, the levels of TNFα and IL6 in PFC+LPS group were significantly decreased (P<005). Meanwhile, the results of ELISA also demonstrated that the levels of IL10 in PFC+LPS group were higher than those in LPS group and PFC could promote IL10 secretion in A549 cells (P<005). The results of Westernblot analysis showed that the protein levels of phosphoNFκB p65 in LPS group were higher than those in normal cell group (P<005). Compared with LPS group, the protein levels of phosphoNFκB p65 in PFC+LPS group were significantly decreased (P<005). Moreover, the results of Westernblot analysis also showed that the protein levels of SIGIRR in PFC+LPS group were higher than those in LPS group and PFC could upregulate the expression of SIGIRR in A549 cells (P<005), conversely, LPS suppressed the expression of SIGIRR in A549 cells. Conclusion PFC could attenuate the LPSinduced inflammation in alveolar epithelial cells. Promotion of IL10 secretion and upregulaiton SIGIRR expression may the possible mechanism of PFC protection against LPSinduce inflammation in alveolar epithelial cells.

    参考文献
    相似文献
    引证文献
引用本文
分享
文章指标
  • 点击次数:
  • 下载次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2017-07-19
您是第位访问者
网站版权所有:《西部医学》编辑部     蜀ICP备18038379号-4
地址:四川省成都市武侯区小天竺街75号财富国际18F-1号    邮政编码:610041
电话:028-85570072/85588403 本网站支持 IPv6    E-mail:xbyxqk@163.com
技术支持:北京勤云科技发展有限公司