首页> 外文期刊>Experimental and therapeutic medicine >Expression of Clara cell 10-kDa protein and trefoil factor family 1 in patients with chronic rhinosinusitis and nasal polyps
【24h】

Expression of Clara cell 10-kDa protein and trefoil factor family 1 in patients with chronic rhinosinusitis and nasal polyps

机译:克拉拉细胞10-KDA蛋白和三叶草因子家庭1在慢性鼻窦炎和鼻息肉患者中的表达

获取原文
获取原文并翻译 | 示例
       

摘要

The current study measured the expression of Clara cell 10-kDa protein (CC10) and trefoil factor family 1 (TFF1) in the sinus mucosa of patients exhibiting chronic rhinosinusitis (CRS) and nasal polyps (NP). CC10 and TFF1 expression in the sinus mucosa of the control group and patients with CRS and NP was determined using reverse transcription-quantitative polymerase chain reaction (RT-qPCR), western blotting and immunohistochemistry. The correlation between CC10 and TFF1 expression was further analyzed using Spearman's correlation analysis. The expression of TFF1 was significantly increased in the sinus mucosa of patients with CRS and NP, whereas CC10 expression was significantly decreased compared with controls. Spearman's correlation analysis identified a negative correlation between CC10 and TFF1 expression in the sinus mucosa of patients with CRS and NP. The results of immunohistochemistry and RT-qPCR were consistent with each other. Hematoxylin and eosin staining revealed notable lesions in the mucous membranes, goblet cells and cilia of sinus mucosa samples from patients with CRS and NP. The negative correlation between CC10 and TFF1 expression during the progression of CRS and NP suggest that CC10 and TFF1 may serve important roles in its pathogenesis.
机译:目前的研究测量了表现出慢性鼻窦炎(CRS)和鼻息肉(NP)的患者的窦粘膜中的克拉拉细胞10-KDA蛋白(CC10)和三叶子因子家族1(TFF1)的表达。使用逆转录定量聚合酶链反应(RT-QPCR),Western印迹和免疫组化测定CC10和CRS和NP患者的窦粘膜和CRS和NP患者的表达。使用Spearman的相关分析进一步分析了CC10和TFF1表达的相关性。 CRS和NP患者的窦粘膜中TFF1的表达显着增加,而CC10表达与对照相比显着降低。 Spearman的相关性分析确定了CC10和CRS和NP患者窦粘膜中的CC10和TFF1表达的负相关性。免疫组织化学和RT-QPCR的结果彼此一致。苏木精和曙红染色揭示了来自CRS和NP患者的粘膜,牙粘膜样品的粘膜,脚葡聚糖细胞和纤毛的显着病变。 CC10和TFF1表达之间的负相关性在CRS和NP进展期间表明CC10和TFF1可以在其发病机制中提供重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号