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Toll样受体2在原发免疫性血小板减少症中的作用研究
引用本文:李慧媛,张冬雷,张岘,付荣凤,宣旻,杨仁池.Toll样受体2在原发免疫性血小板减少症中的作用研究[J].中国实验血液学杂志,2014(4):1033-1037.
作者姓名:李慧媛  张冬雷  张岘  付荣凤  宣旻  杨仁池
作者单位:中国医学科学院、北京协和医学院血液病医院、血液学研究所,天津300020
基金项目:国家自然科学基金(81270581,81300385);协和青年基金和中央高校基本科研业务费专项资金(3332013068)
摘    要:本研究通过检测原发免疫性血小板减少症(ITP)患者外周血淋巴细胞中TLR2的表达,同时评价体外活化TLR2对炎症因子分泌的影响,旨在探讨TLR2在ITP发病机制中的作用.39例ITP患者及21例正常对照者纳入本研究.应用实时定量PCR及流式细胞术检测外周血单个核细胞(PBMNC)中TLR2的表达.采用pam3CSK4体外刺激活化PBMNC,48 h后检测细胞培养上清中IL-6及TNF-α的浓度.结果显示,活动期ITP患者PBMNC中TLR2 mRNA的表达显著高于正常对照(3.561±0.741 vs 1.750±0.314) (P <0.05),而缓解组(2.333±0.448)和正常对照之间TLR2 mRNA差异无统计学意义(P>0.05).流式细胞术分析显示,TLR2在正常对照及ITP患者T、B细胞表面不表达,但表达于所有单核细胞表面.进一步体外实验发现,TLR2活化能诱导ITP患者PBMNC中IL-6(1644±634.0 vs 4111±525.2 pg/ml)及TNF-α (75.37±22.31 vs 326.0±109.9 pg/ml)的表达(P均<0.05),但仅对正常对照PBMNC中IL-6(2119±636.9 vs4671±315.9 pg/ml) (P< 0.05)的分泌有促进作用.结论:TLR2mRNA在ITP患者PBMNC中高表达,这些高表达的TLR2可能通过促进炎症因子的分泌加快ITP疾病进程.

关 键 词:原发免疫性血小板减少症  Toll样受体2  IL-6  TNF-α

Role of Toll-Like Receptor 2 in Primary Immune Thrombocytopenia
LI Hui-Yuan,ZHANG Dong-Lei,ZHANG Xian,FU Rong-Feng,XUAN Min,YANG Ren-Chi.Role of Toll-Like Receptor 2 in Primary Immune Thrombocytopenia[J].Journal of Experimental Hematology,2014(4):1033-1037.
Authors:LI Hui-Yuan  ZHANG Dong-Lei  ZHANG Xian  FU Rong-Feng  XUAN Min  YANG Ren-Chi
Institution:( Institute of Hematology & Blood Disease Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China)
Abstract:The aim of this study was to explore the role of Toll-like receptor (TLR) 2 in primary immune thrombocytopenia (ITP) by detecting TLR2 expression in the peripheral blood lymphocytes of patients with ITP and evaluating the role of TLR2 activation on inflammatory cytokine secretion. A total of 39 ITP patients and 21 normal controls were enrolled in this study. The expression of TLR2 was detected by real-time PCR and flow cytometry, and the concentration of IL-6 and TNF-α in culture supernatant of PBMNC treated with pam3CSK4 for 48 hours were detected by ELISA. The results showed that the expression of TLR2 rnRNA in active ITP patients (3. 561 ±0. 741 ) was significandy higher than that in normal controls (1. 750 ± 0. 314 ) (P 〈 0.05 ), but there was no statistically significant difference between remission ITP patients ( 2.333 ± 0.448 ) and normal controls ( P 〉 0.05 ) . Flow cytometry analysis found that the TLR2 was not expressed on T and B cells, but expressed on all monocytes both from ITP patients and normal controls. Further activation experiment showed that TLR2 activation in vitro could induce the expression of IL-6 ( 1644 ± 634.0 vs 4111 ±525.2 pg/ml) and TNF-α (75.37 ±22.31 vs 326.0 ± 109.9 pg/ml) in PBMNC from ITP patients ( both P 〈 0. 05 ), but just could promote IL-6 expression in normal controls (2119 ± 636.9 vs 4671 ± 315.9 pg/ml) ( P 〈 0.05). It is concluded that the expression of TLR2 mRNA is up-regulated in PBMNC of ITP patients, and this increased TLR2 maybe participate in ITP through inducing secretion of inflammatory cytokines.
Keywords:primary immune thrombocytopenia(ITP)  Toll-like receptor 2  IL-6  TNF-α
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