文章摘要
王晓芬,李福祥,黎俊雅,朱忠立,祝国芸.靶向沉默HIF-1α信号通路抑制百草枯中毒诱导的肺泡上皮细胞上皮间质转化[J].,2018,(13):2419-2423
靶向沉默HIF-1α信号通路抑制百草枯中毒诱导的肺泡上皮细胞上皮间质转化
Paraquat Promotes Epithelial-mesenchymal Transition of Alveolar Epithelial Cells through HIF-1α Signaling Pathway
投稿时间:2017-11-26  修订日期:2017-12-25
DOI:10.13241/j.cnki.pmb.2018.13.004
中文关键词: 百草枯  肺纤维化  缺氧诱导因子-1A  上皮-间质转化
英文关键词: Paraquat  Pulmonary fibrosis  HIF-1α  Epithelial--mesenchymal transition
基金项目:国家自然科学基金项目(81170281)
作者单位E-mail
王晓芬 成都军区总医院重症医学科 四川 成都 610083 shenlan_123_w@126.com 
李福祥 成都军区总医院重症医学科 四川 成都 610083  
黎俊雅 成都军区总医院重症医学科 四川 成都 610083  
朱忠立 成都军区总医院重症医学科 四川 成都 610083  
祝国芸 成都军区总医院重症医学科 四川 成都 610083  
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中文摘要:
      摘要 目的:探讨HIF-1α信号通路在百草枯( paraquat, PQ) 诱导大鼠Ⅱ型肺泡上皮细胞上皮间质转化(Epithelial-mesenchymal tran- sition, EMT)中的作用机制。方法:使用20 μmol /L浓度的百草枯溶剂对大鼠Ⅱ型肺泡上皮RLE-6TN细胞干预24 h,随后在倒置光学显微镜观察各组细胞形态学变化;用real-time PCR与Western blot法检测RLE-6TN细胞中HIF-1α、上皮表型标记蛋白E-cadherin及间质表型标记蛋白Vimentin的表达,Transwell侵袭实验检测各处理组细胞侵袭能力的改变;使用HIF-1α靶向siRNA抑制其表达后,进一步采用RT-PCR和Western blot检测HIF-1α、E-cadherin和Vimentin的表达水平,Transwell法检测细胞侵袭能力变化。结果:体外百草枯溶液可显著诱导大鼠Ⅱ型肺泡上皮细胞RLE-6TN细胞HIF-1α表达升高和上皮间质转化的发生,同时细胞的体外侵袭能力也增强。靶向沉默HIF-1α基因后,百草枯诱导的上皮间质转化过程被逆转,同时细胞侵袭能力显著减弱。结论:百草枯通过调控HIF-1α信号通路来诱导RLE-6TN细胞上皮间质转化的发生,进而促进肺纤维化的形成。
英文摘要:
      ABSTRACT Objective: To investigate the effect of HIF-1α signaling pathway on paraquat (PQ)-induced epithelial-mesenchymal transition (EMT) in rat alveolar type II cells (RLE-6TN) and explore the underlying molecular mechanisms. Methods: RLE-6TN cells were treated by 20 μmol /L PQ, then the morphology was observed by invert light microscope; RT-PCR and Western blot were per- formed to detect the expression level of EMT related markers, E-cadherin and vimentin as well as HIF-1α signaling. Then the Transwell invasion assays was performed to detect the ability of cell invasion. Results: PQ was able to induce the transition of RLE-6TN cells from epithelial morphology to fibroblast-like morphology, associated with the acquisition of migratory properties. Phenotypically, PQ in- duced-EMT was characterized by loss of epithelial cell markers including E-cadherin, while upregulation of mesenchymal cell markers including vimentin, concurrent with the activation of HIF-1α signaling pathway. Furthermore, knockdown of HIF-1α by using specific siRNA could reverse PQ triggered EMT process and attenuated cell migration ability. Conclusion: PQ promoted EMT in rat alveolar type II cells (RLE-6TN) by upregulating the expression of HIF-1α.
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