基础医学与临床 ›› 2015, Vol. 35 ›› Issue (1): 48-53.

• 研究论文 • 上一篇    下一篇

上调miR-200a的表达减弱TGF-β1刺激的大鼠胰腺星状细胞活化和胶原合成

张尤历,王国英,赵义,李萍,刘鑫,倪鑫,徐岷   

  1. 江苏大学附属医院
  • 收稿日期:2014-05-15 修回日期:2014-07-23 出版日期:2015-01-05 发布日期:2014-12-30
  • 通讯作者: 徐岷 E-mail:peterxu1974@163.com
  • 基金资助:
    江苏省自然科学基金;镇江市“169四期工程”科研项目

Up-regulation of miR-200a attenuates TGF-β1-induced activation and collagen synthesis in rat pancreatic stellate cells

  • Received:2014-05-15 Revised:2014-07-23 Online:2015-01-05 Published:2014-12-30
  • Contact: Min XU E-mail:peterxu1974@163.com
  • Supported by:
    Natural Science Foundation of Jiangsu Province of China; The 169 fourth stage project for scientific research projects of Zhenjiang

摘要: 目的 探讨miR-200a对转化生长因子β1(TGF-β1)刺激的大鼠胰腺星状细胞(PSCs)活化和胶原蛋白合成的影响。方法 用组织块法培养分离PSCs,免疫荧光染色检测结蛋白(desmin)、神经胶质原纤维酸性蛋白(GFAP)和α-平滑肌肌动蛋白(?-SMA)的表达鉴定PSCs;取新鲜培养的第2代PSCs,设空白对照组、TGF-β1组、TGF-β1+miR-NC组、TGF-β1+miR-200a mimic组,Western blot法和细胞免疫荧光染色法检测?-SMA和I型胶原蛋白(collagen I)的表达,荧光定量PCR检测a-SMA、collagen I mRNA及miR-200a的表达。结果 TGF-β1可刺激大鼠PSCs活化及促进胶原蛋白的合成(P<0.05),且呈时间依赖性;转染miR-200a mimic后,在相同浓度的TGF-β1刺激下,a-SMA和collagen I的蛋白和mRNA表达明显降低(P<0.01)。结论 上调miR-200a的表达,可减弱TGF-β1对大鼠PSCs活化和胶原蛋白合成的刺激作用,其可能的机制是抑制TGF-β1的生物学作用。

关键词: TGF-β1, PSCs, miR-200a, 纤维化

Abstract: Objective To investigate the effect of miR-200a mimic on transforming growth factor β1-mediated activation and collagen secretion of rat pancreatic stellate cells. Methods PSCs were isolated and cultured from pancreatic tissue and identified by desmin, GFAP and α-SMA immunofluorescence staining. PSCs of 2nd generation were divided into control group, TGF-β1 group, TGF-β1+miR-NC group and TGF-β1+miR-200a mimic group. The levels of a-SMA and collagen I protein were measured by Western blot and immunofluorescence staining. The mRNA levels of a-SMA and collagenⅠ and the expression of miR-200a were detected by quantitative real-time PCR. Results TGF-β1 can stimulate the activation of PSCs and promote collagen synthesis in time-dependment manner (P<0.05). After transfection of the mimic, treating with the same concentration of TGF-β1, the expressions of protein and mRNA of both a-SMA and collagen I decreased significantly (P<0.01). Conclusion Over-expression of miR-200a significantly attenuates a-SMA activity and further affects the collagen synthesis of TGF-β1-dependent activation of PSCs. The mechanisms may inhibit the biological effects of TGF-β1.

Key words: TGF-β1, PSCs, miR-200a, fibrosis

中图分类号: