范延红, 董辉, 潘庆, 郭文怡, 王海昌. TGF-β1在AVP诱导的心肌成纤维细胞表型转化中的作用[J]. 心脏杂志, 2012, 24(1): 7-11. DOI: 10.13191/j.chj.2012.01.13.fanyh.007
    引用本文: 范延红, 董辉, 潘庆, 郭文怡, 王海昌. TGF-β1在AVP诱导的心肌成纤维细胞表型转化中的作用[J]. 心脏杂志, 2012, 24(1): 7-11. DOI: 10.13191/j.chj.2012.01.13.fanyh.007
    FAN Yan-hong, DONG Hui, PAN Qing, GUO Wen-yi, WANG Hai-chang. Role of transforming growth factor β1 in differentiation of cardiac fibroblasts induced by arginine vasopressin[J]. Chinese Heart Journal, 2012, 24(1): 7-11. DOI: 10.13191/j.chj.2012.01.13.fanyh.007
    Citation: FAN Yan-hong, DONG Hui, PAN Qing, GUO Wen-yi, WANG Hai-chang. Role of transforming growth factor β1 in differentiation of cardiac fibroblasts induced by arginine vasopressin[J]. Chinese Heart Journal, 2012, 24(1): 7-11. DOI: 10.13191/j.chj.2012.01.13.fanyh.007

    TGF-β1在AVP诱导的心肌成纤维细胞表型转化中的作用

    Role of transforming growth factor β1 in differentiation of cardiac fibroblasts induced by arginine vasopressin

    • 摘要: 目的:探讨转化生长因子β1(TGF-β1)在精氨酸加压素(AVP)诱导的心肌成纤维细胞(CFs)向肌成纤维细胞(MFs)转化中的作用。方法:用胰酶消化法分离培养SD仔鼠的CFs,将CFs分别与不同浓度的AVP、不同浓度的TGF-β1或添加了不同浓度的抗TGF-β1中和抗体的1×10-6mmol/L AVP共同孵育48 h后,用3H-脯氨酸掺入法检测CFs胶原合成的功能,用Western blot检测CFs中平滑肌肌动蛋白α(α-SMA)的表达量,用ELISA法检测CFs中TGF-β1的合成。结果:AVP可浓度依赖性地诱导CFs的3H-脯氨酸掺入率和α-SMA的表达量增加,其中1×10-6mmol/L AVP组CFs的3H-脯氨酸掺入率和α-SMA的表达量显著高于对照组(P<0.05)。AVP也可浓度依赖性地诱导CFs中内源性TGF-β1的合成增加,其中在1×10-6mmol/L AVP刺激下,CFs合成显著增加的内源性TGF-β1刚好达到外源性TGF-β1诱导CFs向MFs转化所需要的剂量(>2 ng/ml)。抗TGF-β1中和抗体虽然能够显著抑制在10-6mmol/L AVP诱导下CFs的3H-脯氨酸掺入率和α-SMA的表达量(P<0.05),但却不能将其抑制到与对照组相近的水平(P<0.05)。结论:AVP刺激下CFs中内源性TGF-β1合成的增加可部分地介导AVP诱导的CFs向MFs转化。

       

      Abstract: AIM:To investigate the role of transforming growth factor β1(TGF-β1) in the differentiation of cardiac fibroblasts(CFs) into myofibroblasts(MFs) induced by arginine vasopressin(AVP).METHODS:CFs were isolated by trypsin digestion method and co-incubated for 48 h with different concentrations of AVP,different concentrations of TGF-β1,or 1×10-6 mmol/L AVP supplemented with different concentrations of TGF-β1 neutralizing antibody,respectively.3H proline incorporation was used to measure collagen synthesis,Western blot analysis was used to measure α-smooth muscle actin(α-SMA) expression,and ELISA was used to measure TGF-β1 secretion in CFs.RESULTS:AVP induced the increases of 3H proline incorporation and α-SMA expression dose dependently in CFs,and 1×10-6 mol/L AVP notably increased 3H proline incorporation and α-SMA expression compared with those in control group(P<0.05).AVP induced endogenous TGF-β1 secretion of CFs dose dependently,and the notably increased endogenous TGF-β1 induced by 1×10-6 mol/L AVP was well within the range for exogenous TGF-β1 to cause differentiation of CFs into MFs(>2 ng/ml).Although 1×10-6 mol/L AVP-induced increases of 3H proline incorporation and α-SMA expression could be notably inhibited by TGF-β1 neutralizing antibody(P<0.05),they were still higher than those in control group(P<0.05).CONCLUSION:AVP can induce differentiation of CFs into MFs partly through the increase of endogenous TGF-β1 synthesis.

       

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