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中国临床药理学与治疗学 ›› 2014, Vol. 19 ›› Issue (7): 738-742.

• 基础研究 • 上一篇    下一篇

转化生子因子β1对培养心脏成纤维细胞α-SMA及Cx43表达的影响

王新1, 王德国1, 赵春梅1, 邢文1, 王安才1, 朱红军2, 孙贤林2   

  1. 1 皖南医学院附属弋矶山医院老年科,芜湖 241001,安徽;
    2 安徽省立医院心血管内科,合肥 230001,安徽
  • 收稿日期:2014-06-11 修回日期:2014-07-04 发布日期:2014-07-21
  • 通讯作者: 王德国,男,博士, 副主任/副教授,研究方向:心律失常基础与临床研究。 Tel: 0553?5739308  E?mail: wangdeguo@medmail.com.cn
  • 作者简介:王新,女,副主任医师,研究方向:心血管疾病基础与临床。 Tel: 13855362589 E-mail: wangx308@163.com
  • 基金资助:
    国家自然基金(81200142); 省自然科学基金(1208085QH156, 1208085MH129); 医院人才引进科研基金(YR201001)

The effects of TGFβ1 on the expression of α-SMA and Cx43 in cultured cardiac fibroblasts

WANG Xin1, WANG De-guo1, ZHAO Chun-mei1, XING Wen1, WANG An-cai1, ZHU Hong-jun2, SUN Xian-lin2   

  1. 1 Department of Gerontology, Yijishan Hospital of Wannan Medical College, Wuhu 241001, Anhui, China;
    2 Department of Cardiology, Anhui Provincial Hospital , Hefei 231000, Anhui, China
  • Received:2014-06-11 Revised:2014-07-04 Published:2014-07-21

摘要: 目的 本研究拟观察转化生子因子β1(TGFβ1)诱导乳鼠CFs向MFs分化中α-SMA及Cx43表达的影响。方法 酶解-差速贴壁分离法分离培养乳鼠CFs,将 10 ng/mL 的TGFβ1诱导培养第1天细胞;细胞免疫荧光及共聚焦纤维观察α-SMA及Cx43表达;以免疫印迹和RT-PCR分别半定量比较两者α-SMA及Cx43蛋白和mRNA表达。结果 分离培养 2 d 的原代CFs细胞极少表达α-SMA及Cx43蛋白及其mRNA;经TGFβ1诱导 24 h 后α-SMA及Cx43蛋白及其mRNA表达显著增高(P<0.01)。结论 TGFβ1可诱导乳鼠CFs向MFs分化,导致α-SMA及Cx43蛋白及其mRNA表达显著增高。

关键词: 成纤维细胞, 肌成纤维细胞, α-平滑肌肌动蛋白;, 缝隙连接蛋白43, 转化生子因子β1;

Abstract: AIM: To observe the effects of transforming growth factor beta-1(TGFβ1)on the expression of α-smooth muscle actin(α-SMA) and connexin43 (Cx43) in cultured cardiac fibroblasts (CFs). METHODS: CFs were isolated from neonatal rat by trypsin dissociation and differential adhension. Primary cultures of CFs for one day were subjected to TGFβ1 (10 ng/mL) incubation for 24 hours. The expressions of α-SMA and Cx43 were determined by immunofluorescence staining. Semiquantitative analysis of mRNA and protein for α-SMA and Cx43 was finished by RT-PCR (reverse transcription polymerase Chain reaction) and Western blots. RESULTS:Little expression of protein and mRNA levels for α-SMA and Cx43 were observed in cultured 2 days primary CFs. TGFβ1 stimulation for 24 hours led to significantly increased protein and mRNA expression of α-SMA and Cx43.CONCLUSION: Transient TGFβ1 stimulation causes differentiation of CFs into MFs and up-regulations protein and mRNA expression of α-SMA and Cx43.

Key words: cardiac fibroblasts (CFs), myofibroblasts (MFs), α-smooth muscle actin(α-SMA);, connexin43 (Cx43), transforming growth factor beta-1(TGFβ1);

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