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作 者:王雪芹[1] 岳忠勇[2] 李克忠[1] 马金凤[1]
机构地区:[1]山东大学第二医院麻醉科,济南250033 [2]平度市人民医院麻醉科,山东平度266001
出 处:《山东大学学报(医学版)》2013年第6期40-43,共4页Journal of Shandong University:Health Sciences
基 金:山东省科技攻关计划资助课题(2007GG1002005)
摘 要:目的探讨周期性机械牵张对大鼠肺泡巨噬细胞(AM)Toll样受体4(TLR4)表达的影响。方法采用美国Flexercell公司生产的Flexercell 4000TTM应力加载系统,对体外培养的AM进行周期性牵张。实验分为机械牵张6 h组、8 h组(30%应变率,0.3 Hz频率,方波)和静止对照组。RT-PCR检测AM上TLR4 mRNA的表达;ELISA检测巨噬细胞炎性蛋白2(MIP-2)的浓度;免疫细胞化学法检测AM上TLR4蛋白表达。结果与静止对照组比较,机械牵张6 h组、8 h组TLR4 mRNA、MIP-2蛋白及TLR4蛋白表达显著升高(P<0.01)。结论机械牵张导致了大鼠肺泡巨噬细胞TLR4和MIP-2表达上调。Objective To investigate the effects of cyclic mechanical stretch on the expression of Toll-like receptor 4(TLR4) in alveolar macrophages(AM) of rats. Methods Rats’ AM were cyclicly stretched in vitro by using FX4000TTM Cell Stretching Unit produced in Flexercell company of the United States. The AM cells were divided into mechanical stretch of 6h and 8h groups(cyclic mechanical stretch at 30%, frequency of 0.3 Hz and square wave) and static control group. TLR4 mRNA was determined by reverse transcription-polymerase chain reaction (RT-PCR); the concentration of macrophage inflammatory protein 2(MIP-2) was detected by ELISA, while TLR4 protein was determined by immunohistochemistry. Results Expressions of TLR4 mRNA, MIP-2 and TLR4 protein increased significantly in mechanical stretch of 6h and 8h groups compared with those in static control group(P〈0.01). Conclusion Cyclic mechanical stretch upregulates the expressions of TLR4 and MIP-2 in alveolar macrophages of rats.
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