Huang Jun, Wei Chun-yin, Zheng Ze-qi, Wu You-ping, Deng Yu-xiao
Depaartment of Cardiology, First Affiliated Hospital, Jiangxi Medical College, Nanchang 330006, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2006 Aug;22(3):283-7.
To investigate the effects of transforming growth factor-beta1 (TGF-beta1) and signal protein Smad3 on rat myocardial hypertrophy.
The total protein was analysed by flow cytometer assay to judge the hypertrophy of myocardial cell incubated with different level of TGF-beta1 in cultured myocardial cells of neonatal rats. The models of rat cardiac hypertrophy were produced with constriction of the abdominal aorta. At the different time after the operation, the rats were killed, and the left ventricular mass indexes (LVMl) were investigated. The mRNA expressions of TGF-beta1 and Smad3 of cultured cells and hypertrophic left ventricles were assessed by RT-PCR, the protein expressions of Smad3 were assessed by Western blot.
In cultured neonatal myocardial cells, different level TGF-beta1 could significantly increase the total protein, and TGF-beta1 (3 ng/ml) could increase the expression of mRNA and protein of Smad3 and continued for 8 h of cultured cardiomyocytes. The LVMI and the expression of TGF-beta1 mRNA and Smad3 mRNA/protein of hypertrophic left ventricle were increased at the 3rd day after the operation and continued for 4 weeks. The peak expression of them was in 2 weeks after operation.
TGF-beta1 has the effects on rat myocardial hypertrophy, signal protein Smad3 is included in the pathologic progress of rat myocardial hypertrophy.
探讨转化生长因子-β1(TGF-β1)及信号蛋白Smad3对大鼠心肌肥大的影响。
采用流式细胞仪检测新生大鼠培养心肌细胞中不同浓度TGF-β1作用后心肌细胞总蛋白含量,判断心肌细胞肥大情况。采用腹主动脉缩窄法制备大鼠心肌肥大模型,术后不同时间点处死大鼠,检测左心室质量指数(LVMl)。采用逆转录聚合酶链反应(RT-PCR)检测培养细胞及肥大左心室中TGF-β1和Smad3的mRNA表达,采用蛋白质免疫印迹法(Western blot)检测Smad3蛋白表达。
在新生大鼠培养心肌细胞中,不同浓度的TGF-β1均可显著增加总蛋白含量,3 ng/ml的TGF-β1可使Smad3的mRNA和蛋白表达增加,且在心肌细胞培养8 h时仍持续升高。术后第3天,肥大左心室的LVMI及TGF-β1 mRNA和Smad3 mRNA/蛋白表达开始升高,并持续4周,术后2周达到峰值。
TGF-β1对大鼠心肌肥大有影响,信号蛋白Smad3参与大鼠心肌肥大的病理进程。