首页 | 本学科首页   官方微博 | 高级检索  
   检索      

双歧杆菌的完整肽聚糖对大鼠腹腔巨噬细胞TNF-α表达的影响
引用本文:冯聚玲,杨林,姚君,李迎雪,王立生.双歧杆菌的完整肽聚糖对大鼠腹腔巨噬细胞TNF-α表达的影响[J].中国微生态学杂志,2010,22(7):577-579.
作者姓名:冯聚玲  杨林  姚君  李迎雪  王立生
作者单位:暨南大学第二临床医学院,深圳市人民医院,消化科,广东,深圳,518020
基金项目:广东省自然科学基金资助项目,深圳市科技计划重点项目 
摘    要:目的探索双歧双歧杆菌的完整肽聚糖(WPG)对大鼠腹腔巨噬细胞TNF-α的调控作用。方法以WPG刺激大鼠腹腔巨噬细胞;或以NF-κB的抑制剂NAC和ERK抑制剂PD98059分别预先孵育巨噬细胞,再用WPG刺激巨噬细胞,最后用RT-PCR检测巨噬细胞TNF-αmRNA的表达水平。结果 WPG刺激巨噬细胞后,其TNF-αmRNA的表达水平显著高于对照组(P0.01)。但经NAC和PD98059分别预先孵育巨噬细胞后,其TNF-αmRNA的表达水平均明显低于WPG刺激组(P0.01)。结论双歧双歧杆菌的WPG能上调巨噬细胞TNF-αmRNA的表达,这一过程受NF-κB和ERK的调控。

关 键 词:双歧杆菌  完整肽聚糖  巨噬细胞

Regulation of whole peptidoglycan of Bifidobacteria on TNF-α of rat peritoneal macrophages
FENG Ju-ling,YANG Lin,YAO Jun,LI Ying-xie,WANG Li-sheng.Regulation of whole peptidoglycan of Bifidobacteria on TNF-α of rat peritoneal macrophages[J].Chinese Journal of Microecology,2010,22(7):577-579.
Authors:FENG Ju-ling  YANG Lin  YAO Jun  LI Ying-xie  WANG Li-sheng
Institution:FENG Ju-ling,YANG Lin,YAO Jun,LI Ying-xie,WANG Li-sheng(Department of Gastroenterology,The Second Clinical Medical Hospital of Jinan University,Shenzhen 518020,China)
Abstract:Objective To explore the regulation of whole peptidoglycan(WPG) of Bifidobacteria bifidum on TNF-α of rat peritoneal macrophages.Method Rat peritoneal macrophages were stimulated by WPG.The macrophages were pretreated with NF-κB inhibitor NAC and ERK inhibitor PD98059 respectively,then stimulated by WPG.The expression of TNF-α mRNA of the macrophages was detected by using RT-PCR.Result After the macrophages were stimulated by WPG,its expression level of TNF-α mRNA was obviously higher when compared with control group(P 0.01).After the macrophages were pretreated with NAC and PD98059 respectively,its expression level of TNF-α mRNA was markedly lower when compared with WPG stimulating group(P 0.01).Conclusion The WPG of Bifidobacteria bifidum can upregulate the expression of TNF-α mRNA of macrophages through NF-κB and ERK.
Keywords:Bifidobacterium  Whole peptidoglycan  Macrophage  
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号