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热休克因子1基因转染对烧伤血清刺激的巨噬细胞炎性介质表达的影响
引用本文:罗成群,尹朝奇,周建大,贺全勇,朱颉,李萍,陈铁夫,彭浩,徐阳成,陈佳.热休克因子1基因转染对烧伤血清刺激的巨噬细胞炎性介质表达的影响[J].中华烧伤杂志,2007,23(5):331-334.
作者姓名:罗成群  尹朝奇  周建大  贺全勇  朱颉  李萍  陈铁夫  彭浩  徐阳成  陈佳
作者单位:中南大学湘雅三医院烧伤整形科,长沙,410011
基金项目:国家自然科学基金(30672035)
摘    要:目的了解外源性热休克因子1(HSF1)对烧伤血清刺激的巨噬细胞中相关炎性介质基因表达的影响。方法制备严重烧伤和正常大鼠血清;构建pcDNA3.1/HSF1重组载体。将培养的RAW264.7巨噬细胞株转染(具体分为:未转染、转染空载体、转染重组载体)后再分别使用前述2种血清刺激。另取部分未行血清刺激的转染重组载体的巨噬细胞,用蛋白质印迹法检测其HSF1蛋白表达水平;反转录-PCR法检测经血清刺激的细胞中肿瘤坏死因子α(TNF-α)、高迁移率族蛋白B1(HMGB1)和白细胞介素10(IL-10)基因表达水平。结果已转染重组载体的细胞株较稳定,检出有HSF1部分活化。反转录-PCR检测到,未转染的正常血清刺激的巨噬细胞中TNF—α、HMGB1、IL-10的基因仅有少量表达,而烧伤血清刺激能明显上调其基因表达(分别为0.910±0.100、0.860±0.020、0.430±0.010);与转染空载体+烧伤血清组(上述3项指标分别为0.800±0.050、0.880±0.030、0.420±0.010)比较,转染重组载体+烧伤血清组可明显抑制巨噬细胞中TNF—α和HMGB1的基因表达并上调IL-10的基因表达(分别为0.130±0.100、0.450±0.020、0.450±0.020)。结论严重烧伤后给予HSF1可以抑制巨噬细胞产生的某些促炎介质的表达,适当上调某些抗炎介质的表达,对机体发挥保护作用。

关 键 词:烧伤  血清  热休克蛋白质类  巨噬细胞  转染  白细胞介素10  肿瘤坏死因子α  高迁移率族蛋白质类
修稿时间:2007-01-31

Influence of heat shock factor 1 gene transfection on the expression of inflammatory mediators in macrophages induced by burn serum
LUO Cheng-qun,YIN Chao-qi,ZHOU Jian-da,HE Quan-yong,ZHU Jie,LI Ping,CHEN Tie-fu,PENG Hao,XU Yang-cheng,CHEN Jia.Influence of heat shock factor 1 gene transfection on the expression of inflammatory mediators in macrophages induced by burn serum[J].Chinese Journal of Burns,2007,23(5):331-334.
Authors:LUO Cheng-qun  YIN Chao-qi  ZHOU Jian-da  HE Quan-yong  ZHU Jie  LI Ping  CHEN Tie-fu  PENG Hao  XU Yang-cheng  CHEN Jia
Institution:Department of Burns and Plastic Surgery, the Third Xiangya Hospital of Central South University, Changsha 410013 , P. R. China
Abstract:OBJECTIVE: To investigate the influence of heat shock factor1 (HSF1) on gene expression of inflammatory mediators in RAW264.7 murine macrophage cells induced by burn serum. METHODS: Sera were separated from blood of normal rats and rats with severe burns, and the recombinant vector pcDNA3. 1/HSF1 was constructed. RAW264.7 macrophages were divided into non-transfection group, vacant vector group (with burn and normal sera stimulation, respectively after vacant vector transfection) and recombinant vector group (with burn and normal sera stimulation, respectively after recombinant vector transfection). Some recombinant vector transfected macrophages without serum stimulation were prepared for the determination of HSF 1 expression with Western blotting. The mRNA expressions of TNF-alpha, HMGB 1 and IL-10 were determined with RT-PCR. RESULTS: The cell line attained after recombinant vector transfection was comparatively stable,with partial activation of HSF 1. Burn sera markedly upregulated TNF-alpha, HMGB1 mRNA expression (0.910 +/- 0.100, 0.860 +/- 0.020, respectively), but downregulated IL-10 expression (0.430 +/- 0.010, respectively) in normal macrophages, while these genes maintained in a very low level in normal macrophages with normal serum stimulation . macrophages with recombinant vector transfection and burn serum stimulation could obviously inhibit the expression of TNF-alpha and HMGB 1, but enhance the IL-10 gene expression (0.130 +/- 0.100, 0.450 +/- 0.020 , 0.450 +/- 0.020, respectively )when compared with that with vacant vector transfection and burn serum stimulation (0.800 +/- 0.050, 0.880 +/- 0.030, 0.420 +/- 0.010, respectively). CONCLUSION: HSF1 can inhibit the expression of some pro-inflammatory mediators in macrophages after a severe burns, indicating that appropriate upregulation of anti-inflammtory mediators might exert protective effects on the organism.
Keywords:Burns  Serum  Heat shock proteins  Macrophages  Transfection  Interleukin 10  Tumor necrosis factor alpha  High mobility group box proteins
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