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鼻息肉组织中固生蛋白C的表达与转化生长因子β1的关系
引用本文:刘争,游学俊,张松,高起学,崔永华.鼻息肉组织中固生蛋白C的表达与转化生长因子β1的关系[J].中华耳鼻咽喉头颈外科杂志,2005,40(6):452-457.
作者姓名:刘争  游学俊  张松  高起学  崔永华
作者单位:1. 430030,武汉,华中科技大学同济医学院附属同济医院耳鼻咽喉科
2. 430030,武汉,华中科技大学同济医学院附属协和医院耳鼻咽喉科
摘    要:目的探讨细胞外基质(extracellularmatrix,ECM)成分固生蛋白C(tenascinC,TNC)在鼻息肉组织中异常表达的原因。方法采用免疫组化方法检测TNC和转化生长因子β1(transforminggrowthfactor-β1,TGF-β1)在鼻息肉组织中的表达和关系。进一步采用细胞培养、实时定量RTPCR和原位ELISA技术研究TGFβ1及嗜酸粒细胞对人呼吸道上皮细胞系BEAS2B细胞TNC表达的调控作用。结果①TNC和TGF-β1蛋白在鼻息肉组织中的表达显著上调,TNC表达强度与TGFβ1阳性细胞总数(r=-0.58,P<0.01)和TGFβ1阳性的嗜酸粒细胞数显著相关(r=-0.61,P<0.01);②浓度为1ng/ml和10ng/ml的TGFβ1刺激4h后BEAS2B细胞TNCmRNA的表达分别为未刺激状态下的(7.20±3.43,x±s,下同)倍和(22.48±5.35)倍,与未刺激状态下的表达水平相比差异有统计学意义(P值<0.01);与刺激24h后TNC蛋白表达的荧光强度相比差异亦有统计学意义(P<0.05);③BEAS2B细胞和嗜酸粒细胞以2∶1、1∶1和1∶2的数量比例进行共培养,4h后BEAS2B细胞TNCmRNA的表达与未刺激状态下的表达水平相比,差异均有统计学意义(P值均<0.01);24h后TNC蛋白表达的荧光强度与未刺激状态下的荧光强度相比差异亦均有统计学意义(P值均<0.05);嗜酸粒细胞的这种诱导作用可以被抗TGFβ1的中和抗体显著抑制(P<0.05)。结论TGF-β1和嗜酸粒细胞可以诱导呼吸道上皮细胞对TNC的表达,嗜酸粒细胞的作用部分通过TGFβ1介导,鼻息肉组织中TNC表达的增高同嗜酸粒细胞来源的TGF-β1有关。

关 键 词:鼻息肉组织  转化生长因子β1  蛋白C  嗜酸粒细胞  定量RT-PCR  TGF-β1蛋白  原位ELISA  呼吸道上皮细胞  matrix  免疫组化方法  荧光强度  TNC  mRNA  蛋白表达  细胞外基质  上皮细胞系  B细胞  统计学  异常表达  细胞培养  调控作用
修稿时间:2004年10月28

Relationship between the expression of tenascin C and TGF-β1 in human nasal polyp tissues
LIU Zheng,YOU Xue-jun,ZHANG Song,GAO Qi-xue,CUI Yong-hua.Relationship between the expression of tenascin C and TGF-β1 in human nasal polyp tissues[J].Chinese JOurnal of Otorhinolaryngology Head and Neck Surgery,2005,40(6):452-457.
Authors:LIU Zheng  YOU Xue-jun  ZHANG Song  GAO Qi-xue  CUI Yong-hua
Institution:Department of Otorhinolaryngology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China. Zhengliuent@hotmail.com
Abstract:OBJECTIVE: To explore the mechanism underlying the increased expression of tenascin C (TNC) in human nasal polyp tissues. METHODS: The method of immunohistochemistry was used to detect the protein expression of TNC and transforming growth factor-beta1 (TGF-beta1) and their relationship in nasal polyp tissues. The cell culture, real-time RT-PCR and in situ ELISA techniques were employed to investigate the effect of TGF-beta1 and eosinophils on the TNC mRNA and protein expression in BEAS-2B immortalized human bronchial epithelial cells. RESULTS: (1) TNC and TGF-beta1 protein expression were up-regulated in nasal polyp tissues. TNC expression level was associated with the number of TGF-beta1 positive cells (r = -0.58, P < 0.01) and TGF-beta1 positive eosinophils (r = -0.61, P < 0.01); (2) 1 ng/ml and 10 ng/ml TGF-beta1 induced TNC mRNA expression by 7.20 +/- 3.43-fold and 22.48 +/- 5.35-fold (P < 0.01) in BEAS-2B cells after 4 h stimulation respectively. The fluorescence intensity of TNC protein expression was 129. 50 +/- 47.42 and 151.20 +/- 48.36 after 24 h stimulation respectively. The protein expression was significantly increased compared with that without stimulation (60.60 +/- 38.53, P < 0.05); (3) Coculture BEAS-2B cells and eosinophils at 2:1, 1:1 and 1:2 ratio, TNC mRNA expression was induced by 4.90 +/- 1.40-fold, 5.48 +/- 1.60-fold and 4.78 +/- 1.32-fold (P < 0.01) in BEAS-2B cells after 4 h coculture respectively. The fluorescence intensity of TNC protein expression was 128.75 +/- 44.15, 142.33 +/- 29.06 and 131.33 +/- 20.87 after 24 h coculture respectively. The protein expression was significantly increased compared with that without eosinophils coculture (59.40 +/- 10.14, P < 0.05). Treatment with neutralizing antibody to TGF-beta1 significantly inhibited eosinophil-induced BEAS-2B cells TNC expression in a dose-dependent manner (P < 0.05). CONCLUSION: TGF-beta1 and eosinophlis can induce TNC expression in airway epithelial cells. The effect of eosinophils is partially mediated through TGF-beta1. Up-regulated expression of TNC in nasal polyp tissues is related to eosinophil-derived TGF-beta1.
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