文章摘要
陈恩竹1 田刚1 刘凤娟1 于文成2 李金凤2.TLR-4 在慢性阻塞性肺病患者肺组织表达的研究[J].,2012,12(12):2345-2348
TLR-4 在慢性阻塞性肺病患者肺组织表达的研究
The Expression of TLR-4 in Patients with Chronic ObstructivePulmonary Disease
  
DOI:
中文关键词: 肺疾病  慢性阻塞性  气道炎症  TOLL-4 样受体
英文关键词: Pulmonary disease  Chronic obstructive  Airway innammation  Toll-like receptors
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作者单位
陈恩竹1 田刚1 刘凤娟1 于文成2 李金凤2 青岛大学医学院 
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中文摘要:
      目的:观察COPD 患者肺组织中TLR-4,IL-8,MUC5AC 的表达,并探讨其在气道炎症、气道高分泌中的作用。方法:非 COPD、COPD 组男性肺癌病人各20 例,取其肺叶切除后的外周肺组织,对肺组织标本行HE 及AB-PAS 染色,用免疫组织化学方 法检测肺组织中TLR-4,IL-8,MUC5AC 的表达并分析其相关性。结果:①COPD 患者肺组织中TLR-4,IL-8,MUC5AC 表达较对 照组增高(P<0.05)。TLR-4 主要在气道上皮细胞、肺巨噬细胞及血管内皮细胞表达,IL-8 在气道壁、肺泡间隔、血管壁及肺组织内 浸润的单核细胞、巨噬细胞、多形核白细胞均有表达,MUC5AC 主要在气道上皮杯状细胞中表达。②TLR-4、IL-8 表达与气道炎细 胞评分成正相关(P<0.05)。TLR-4 与IL-8、MUC5AC 表达成正相关(P<0.05)。结论:COPD 患者肺组织中TLR-4 高表达可能参与了 COPD 的气道炎症及气道高分泌,这可能是通过增加IL-8 与MUC5AC 的表达来实现的。
英文摘要:
      Objective: To test the expression of TLR-4 in patients with chronic obstructive disease,and to explore the role of TLR4 in airway innammation and mucus hypersecretion of COPD pathogenesis.Methods: Lung specimens from patients without COPD(non- COPD group) and patients with COPD (COPD group). 20 in each group were investigated.All lung specimens was observed by HE and AB-PAS staining. The expression of TLR-4, IL-8, MUC5AC were observed by immunohistochemical staining. Results:①The expression of TLR-4,IL-8 and MUC5AC in COPD group were higher than those in control group(P<0.05). TLR-4 major express in airway epithelial cells, pulmonary macrophage and vascular endothelial cells. IL-8 express in airway walls, alveolar interval, hemal wall and mononuclear cells, macrophages, nucleation white blood cells which infiltrate in lung issue . MUC5AC mainly express in the goblet cells of airway epithelial.②TLR-4, IL-8 were positively correlated with airway inflammatory cells score( P<0.05). TLR-4 was positively correlated with IL-8and MUC5AC (P<0.05). Conclusion: The high expression of TLR-4 probably involved in airway innammation and mucus hypersecretion of COPD pathogenesis. This may be achieved by increasing the expression of IL-8 and MUC5AC.
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