首页  期刊介绍 征稿简则 编委会 期刊征订 广告服务 留言板 联系我们 English

中国应用生理学杂志 ›› 2018, Vol. 34 ›› Issue (3): 249-253.doi: 10.12047/j.cjap.5615.2018.059

• 研究论文 • 上一篇    下一篇

降钙素基因相关肽对大鼠肺泡上皮Ⅱ型细胞间质转分化的作用及机制

李先伟1, 蒋莉莉1, 左东泽1, 郝伟1, 吴海龙2   

  1. 1. 皖南医学院药理学教研室 安徽省多糖药物工程技术研究中心, 芜湖 241002;
    2. 安徽师范大学生命科学学院, 芜湖 241000
  • 收稿日期:2017-07-10 修回日期:2017-11-20 出版日期:2018-05-28 发布日期:2018-09-08
  • 通讯作者: 吴海龙,Tel:0533-3883591;E-mail:whlong@mail.ahnu.edu.cn E-mail:whlong@mail.ahnu.edu.cn
  • 基金资助:
    安徽省高校优秀青年人才支持计划重点项目(gxyqZD2016170)

Effects of calcitonin gene-related peptide on epithelial-mesenchymal transition of alveolar epithelial cells in rat and its mechanism

LI Xian-wei1, JIANG Li-li1, ZUO Dong-ze1, HAO Wei1, WU Hai-long2   

  1. 1. Department of Pharmacology, Wannan Medical College, Anhui Provincial Engineering Technology Research Center for Polysaccharide Drugs, Wuhu 241002;
    2. College of Life Sciences, Anhui Normal University, Wuhu 241000, China
  • Received:2017-07-10 Revised:2017-11-20 Online:2018-05-28 Published:2018-09-08
  • Supported by:
    安徽省高校优秀青年人才支持计划重点项目(gxyqZD2016170)

摘要: 目的:观察降钙素基因相关肽(CGRP)对大鼠肺泡上皮细胞间质转分化(EMT)的作用并探讨其机制。方法:实验设Control组、TGF-β1(5 ng/ml)、CGRP (1、10、100 nmol/L)组、CGRP8-37(1 μmol/L)+CGRP (100 nmol/L)组。每组设9个复孔。细胞分别用CGRP或加CGRP8-37预处理1 h,再用转化生长因子β1(TGF-β1)处理48 h。MTT法检测大鼠肺泡上皮Ⅱ型细胞(RLE-6TN细胞)活性。分别采用Real-time PCR和Western blot检测细胞E-cadherin、α-SMA、eIF3a、Notch1和collagen Ⅲ mRNA及蛋白表达。结果:与TGF-β1(5 ng/ml)相比,不同剂量CGRP (1、10、100 nmol/L)均可明显提高RLE-6TN细胞活性,显著抑制eIF3a、Notch1、α-SMA及collagen Ⅲ胶原的表达,上调E-cadherin的表达,而CGRP的这些作用可以被CGRP阻断剂CGRP8-37所取消。结论:CGRP对EMT具有一定的抑制作用,其机制可能与其抑制Notch1、eIF3a表达有关。

关键词: 降钙素基因相关肽, 上皮细胞间质转分化, eIF3a, Notch1, 大鼠

Abstract: Objective: To observe the effects of calcitonin gene-related peptide (CGRP) on epithelial-mesenchymal transition (EMT) of alveolar epithelial cells and its mechanism.Methods: The RLE-6TN cell were divided into 6 groups as follows:control group, cells were incubated with double distilled water (TGF-β1 solvent) for 48 h; transforming growth factor-β1(TGF-β1) group, cells were incubated with TGF-β1 (5 ng/ml) for 48 h; +CGRP (1, 10,100 nmol/L) group, cells were pre-treated with CGRP (1, 10,100 nmol/L) for 1 h, and then subjected to TGF-β1 for 48 h; CGRP 100 nmol/L + CGRP8-37 1 μmol/L group, cells were pre-treated with CGRP 100 nmol/L + CGRP8-37 1 μmol/L for 1 h, and then subjected to TGF-β1 for 48 h. RLE-6TN cell vitality was determined by MTT. The mRNA or protein expression levels of Notch1, eIF3a, α-SMA, E-cadherin and collagen Ⅲ were detected by real-time PCR or Western blot.Results: Compared with the TGF-β1 group, cell vitality and the expression of E-cadherin were significantly increased, and the expression of Notch 1, eIF3a, α-SMA and collagen Ⅲ were markedly decreased in CGRP (1, 10, 100 nmol/L) group. The effects of CGRP above mentioned could be abolished by CGRP 8-37.Conclusion: These results suggest that CGRP inhibits TGF-β1-induced EMT process, and down-regulation of the expressions of Notch1and eIF3a may be involved in its mechanisms.

Key words: calcitonin gene-related peptide, epithelial-mesenchymal transition, Notch1, eIF3a, rat

版权所有 © 2015 《中国应用生理学杂志》编辑部
京ICP备16058274号-1
地址:天津市和平区大理道1号,邮编:300050  电话:022-23909086  E-mail:editor@cjap.ac.cn
本系统由北京玛格泰克科技发展有限公司设计开发 技术支持:support@magtech.com.cn