基础医学与临床 ›› 2017, Vol. 37 ›› Issue (9): 1297-1302.

• 研究论文 • 上一篇    下一篇

胡椒碱抑制AngⅡ诱导大鼠气道平滑肌细胞增殖和迁移

刘翠翠1,石晓岚2,赵龙1,王宁1,马彩玲1   

  1. 1. 西安市儿童医院
    2. 西安市儿童医院呼吸哮喘科
  • 收稿日期:2016-08-18 修回日期:2016-11-03 出版日期:2017-09-05 发布日期:2017-08-28
  • 通讯作者: 刘翠翠 E-mail:cbaoqing@163.com

Piperine inhibits Ang II-induced cell proliferation and migration in airway smooth muscle cells

  • Received:2016-08-18 Revised:2016-11-03 Online:2017-09-05 Published:2017-08-28

摘要: 目的 探究胡椒碱对血管紧张素II(Ang II)对大鼠气道平滑肌细胞(ASMCs)增殖和迁移的影响。方法 用改良组织块和胰蛋白酶消化联合培养原代细胞ASMCs。MTT检测Ang II及其受体拮抗剂losartan对细胞增殖活性的影响。Ang II和不同浓度胡椒碱作用ASMCs后,MTT、流式细胞术、Transwell分别检测细胞增殖、细胞周期以及细胞迁移;ERK1/2抑制剂PD98059和losartan干预后,Western blot检测cyclin D1、MMP-9、p-ERK1/2、ERK1/2和β-actin等蛋白表达。结果 Ang II(10-8、10-7、10-6和10-5 mol/L)作用24 h后,可浓度依赖性地促进ASMCs增殖(P<0.05),其中10-7 mol/L Ang II促进效果最为显著;losartan处理则抑制Ang II诱导的ASMCs增殖(P<0.05)。10-7 mol/L Ang II处理组ASMCs增殖活性、S期细胞分布比例、细胞迁移数目、蛋白质(cyclin D1、MMP-9和p-ERK1/2)表达均明显增加(P<0.05);而胡椒碱(10、25、50和100 μmol/L)处理可浓度依赖性地减轻Ang II诱导的上述效应。并且PD98059和losartan亦能阻断Ang II对ASMCs p-ERK1/2、cyclin D1和MMP-9的上调作用。结论 胡椒碱能通过ERK1/2通路抑制Ang II诱导的大鼠ASMCs增殖和迁移。

Abstract: Objective To explore the effects of piperine on cell proliferation and migration in angiotensin II (Ang II)-treated rat airway smooth muscle cells (ASMCs). Methods The primary ASMCs of rats were cultured by improved tissue-piece digestion inoculation and trypsin digestion. MTT assay was used to detect the effects of Ang II and Ang II receptor antagonist losartan on cell proliferation activity. After treatment with Ang II and piperine, the cell proliferation activity, the cell cycle distribution and the cell migration were detected by MTT, flow cytometry and Transwell assay, respectively. ERK1/2 inhibitor PD98059 and losartan were then introduced to determine the expression of cyclin D1, MMP-9, p-ERK1/2, ERK1/2, and β-actin proteins by western blot assay. Results After 24 h culture, Ang II treatment dose-dependently promoted the cell proliferative activity in rat ASMCs (P<0.05), and the promotive effect of 10-7 mol/L Ang II was the most significant. Additionally, losartan blocked the Ang II-induced cell proliferative activity in rat ASMCs (P<0.05). 10-7 mol/L Ang II treatment resulted in the elevated cell proliferative activity, higher S phase fraction, increased migrated cell number, and enhanced expression of cyclin D1, MMP-9 and p-ERK1/2 proteins (P<0.05); these effects were dose-dependently reversed by piperine. Both PD98059 and losartan blocked Ang II-induced expression of p-ERK1/2, cyclin D1 and MMP-9 proteins in rat ASMCs. Conclusions Piperine may inhibit Ang II-induced cell proliferation and cell migration via ERK1/2 signaling pathway in rat ASMCs.