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作 者:陈益国[1] 黄钊霞[2] 卢晓[2] 侯晓睿[2] 王湘豫[2] 富宁[2] 刘北一[2]
机构地区:[1]江西省人民医院检验科,南昌330006 [2]南方医科大学基础医学院免疫学教研室,广州510515
出 处:《中国免疫学杂志》2013年第10期1017-1021,共5页Chinese Journal of Immunology
基 金:江西省自然科学基金(No.20132BAB205049);广东省自然科学基金(No.S2012010009562)资助
摘 要:目的:初步探讨TLR2激动剂Pam3Csk4预处理后,小鼠腹腔巨噬细胞对肺炎克雷伯菌(Klebsiella pneumoniae,K.p)的免疫反应性。方法:1μg/ml Pam3CSK4于0小时作用鼠腹腔巨噬细胞,24小时后以不同剂量热灭活肺炎克雷伯菌刺激细胞,ELISA检测细胞培养上清中TNF-α、IL-6含量,比色法检测NO含量,流式检测小鼠腹腔巨噬细胞对热灭活K.p的吞噬能力;RT-PCR和流式检测细胞表面TLR2表达。结果:肺炎克雷伯菌刺激后,Pam3Csk4预处理组TNF-α、IL-6、NO分泌量显著低于未处理组(P<0.05),Pam3Csk4预处理组细胞对K.p吞噬能力显著降低(P<0.05),巨噬细胞表面TLR2及其基因水平表达量均降低。结论:Pam3Csk4预处理小鼠腹腔巨噬细胞能降低其对肺炎克雷伯菌的免疫反应。Objective:To investigate the immune response of murine peritoneal macrophage pretreated with TLR2 agonist Pam3Csk4 to Klebsiella pneumoniae (K. p). Methods: Murine peritoneal macrophages were pretreated with Pam3Csk4 (I μg/ml). Following pretreatment 24 h later, heat-killed K. p (HK-K. p ) was added and incubated for 12 hours. The concentrations of TNF-α, IL-6 and nitric oxide (NO) were determined by ELISA and colorimetry, respectively. Meanwhile, the expression of TLR2 was assessed by RT-PCR and flow cytometry. To estimate phagocytosis of macrophage, HK-K. p labeled with FITC (FITC-HK-K. p) was added into the well and incubated for 30 rain. After washing 5 times with PBS, intracellular FITC-HK-K. p was detected by flow cytometry. Re- sults : Compared with the control, the secretion of TNF-α, IL-6 and NO released from pretreated cells was diminished respectively, and the phagocytosis was reduced in macrophages pretreated with Pam3Csk4 after stimulated with HK-K. p. The macrophages pretreated with Pam3Csk4 had lower TLR2 expression. Conclusion: Murine peritoneal macrophages were hypo-responsive to Klebsiella pneumo- nia after pretreatment with low-dose TLR2 agonist.
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