脂多糖诱导肥大细胞释放HMGB1研究  被引量:3

Extracellular release of HMGB1 in lipopolysaccharide-induced mast cells and related signaling pathways

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作  者:杨岚[1] 李蕾[2] 邵俊良[2] 许飞[1] 陈国千[2] 

机构地区:[1]南京医科大学附属无锡妇幼保健院检验科,江苏无锡214002 [2]南京医科大学附属无锡人民医院医学检验科,江苏无锡214023

出  处:《南京医科大学学报(自然科学版)》2010年第7期919-922,共4页Journal of Nanjing Medical University(Natural Sciences)

基  金:江苏省自然科学基金资助(BK2006027)

摘  要:目的:研究脂多糖(LPS)对肥大细胞高迁移率族蛋白B1(HMGB1)释放的诱导作用及其胞内信号通路。方法:采用小鼠肥大细胞株P815,观察不同剂量LPS诱导后细胞培养上清液中HMGB1含量和细胞HMGB1mRNA表达水平的变化,及不同剂量丝裂原活化蛋白激酶(MAPK)信号通路抑制剂(SB203580、SB202190、U0126和PD98059)对LPS诱导后HMGB1胞外释放的影响。HMGB1含量采用酶联免疫吸附试验检测。结果:LPS诱导后细胞培养上清液中HMGB1含量明显升高,并与LPS剂量、诱导时间有关;100μg/LLPS分别诱导8、24、48h后,HMGB1mRNA表达水平明显增强(P<0.01);SB203580和SB202190对LPS诱导HMGB1释放有明显的抑制作用(P<0.05),但U0126和PD98059不显示抑制作用。结论:LPS诱导肥大细胞释放HMGB1,其释放机制与胞内p38MAPK信号通路有关。Objective:To study the extracellular release of high mobility group box 1(HMGB1)in mast cells induced by lipopolysaccharide(LPS)and related intracellular signaling pathways.Methods:The changes of HMGB1 concentration in the culture medium and HMGB1 mRNA expression of P815 mast cells were investigated using enzyme-linked immunosorbent assay(ELISA)and RT-PCR method after stimulation with various concentrations of LPS.The effects of MAPKs pathway inhibitors(SB203580,SB202190,U0126 and PD98059)on extracellular release of HMGB1 were observed in LPS-induced mast cells.Results:LPS induced extracellular release of HMGB1 in mast cells in a dose-and time-dependent manner.The level of HMGB1 mRNA expression significantly was increased by stimulation with 100 μg/L LPS for 8,24 or 48 hours(P0.01).SB203580 and SB202190 partly inhibited HMGB1 release in LPS-induced mast cells(P0.05).But no effects were observed in U0126 and PD98059 treated group.Conclusion:LPS can induce mast cells to release HMGB1,in which the intracellular p38 MAPK signaling pathway is involved.

关 键 词:高迁移率族蛋白B1 肥大细胞 内毒素 丝裂原活化蛋白激酶 

分 类 号:R392.12[医药卫生—免疫学]

 

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