基础医学与临床 ›› 2011, Vol. 31 ›› Issue (2): 179-182.

• 研究论文 • 上一篇    下一篇

褪黑素促进哮喘小鼠肺组织STAT4的表达及抑制气道炎症

王敏,李美容,张光环,熊安秀   

  1. 三峡大学第一临床医学院宜昌市中心人民医院
  • 收稿日期:2010-05-10 修回日期:2010-06-28 出版日期:2011-02-05 发布日期:2011-03-14
  • 通讯作者: 王敏 E-mail:wmin120@yahoo.com.cn
  • 基金资助:
    市攻关计划

Melatonin promotes the expression of STAT4 and inhibite airway inflammation in asthmatic mouse

  1. 1. The First College of Clinical Medical Science,China Three Gorges University;Yichang Central People′s Hospital
    2.
  • Received:2010-05-10 Revised:2010-06-28 Online:2011-02-05 Published:2011-03-14
  • Contact: WANG Min E-mail:wmin120@yahoo.com.cn

摘要: 目的 探讨褪黑素(MT)对哮喘小鼠肺组织信号转导子和转录激活子4(STAT4)表达的影响及其在气道炎症中的作用。方法 最后1次雾化激发后1h行左肺支气管肺泡灌洗计数炎性细胞;免疫组织化学和实时定量PCR分别检测右肺组织STAT4蛋白及其mRNA的表达;酶联免疫吸附试验检测外周血 IL-12水平。结果 (1)模型组小鼠支气管肺泡灌洗液(BALF)中炎性细胞总数和EOS较对照组明显增多,肺组织STAT4蛋白及其mRNA表达较对照组明显降低;MT组以上指标均得到明显缓解(P <0.01);(2)哮喘小鼠STAT4蛋白及其mRNA的表达均与BALF中EOS呈高度负相关(r=-0.754, r=-0.755; P <0.01),外周血IL-12水平与STAT4蛋白表达呈高度正相关(r=0.742, P <0.01)。结论 MT能通过诱导哮喘小鼠肺组织STAT4基因的转录、翻译,促进外周血IL-12产生,抑制EOS等炎性细胞浸润,显著抑制气道炎症。

关键词: STAT4, 褪黑素, 哮喘, 气道炎症

Abstract: Objective To investigate the effect of melatonin (MT) on signal transduce and activator of transcription 4(STAT4)and its airway inflammation in asthmatic mice. Methods At 1h after the last aerosol exposure, the left lungs were lavaged, the number of inflammatory cell in the mouse bronchoaleolar lavage fluids (BALF) were counted with microscope. Using immunohi- stochemistry and real-time fluorescent quantitative PCR to detect expression of STAT4 protein and its mRNA expressionism in right lung tissue. Using enzyme-linked immunosorbent assay to detecte levels of IL-12 in serum. Results (1) In model group, the number of inflammatory cells and EOS were significantly higher than control group, STAT4 protein and STAT4mRNA expression in lung tissue was significantly decreased when compared with control group. MT treated group significantly alleviated the above-mentioned parameters.And there were significant differences between MT treated group and control group,DXM treated group and model group. (P<0.01). (2)In asthmatic mice, STAT4 protein and its mRNA expression had both altitude negative relationship with EOS counts in BALF (r=0.849, P<0.01; r=0.972, P<0.01, respectively). Levels of IL-12 in serum had altitude positive correlation with STAT4 protein expression in asthmatic group mice(r=0.742, P<0.01). Conclusion MT may be through inducing STAT4 gene transcription and translation in asthmatic mice, promoting production of IL-12 in peripheral blood,inhibiting inflammatory cell infiltration,significantly reduce the airway inflammation.

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