Department of Cardiology, the Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.
Acta Biochim Biophys Sin (Shanghai). 2012 Nov;44(11):902-10. doi: 10.1093/abbs/gms085. Epub 2012 Oct 11.
Epithelial-mesenchymal transition (EMT) is an important mechanism of cardiac fibrosis after myocardial infarction (MI). However, it remains unclear whether Snail1, an important regulator of EMT, is involved in cardiac fibrosis. In this study, we explored the expression patterns of Snail1 and a cardiac fibrosis marker-periostin-after MI in mice and then investigated the co-expression between Snail1 and periostin after MI in mice. Our results showed that the mRNA and protein levels of Snail1 and periostin were significantly increased in the infarct area. The Snail1 expression pattern appeared to be parabolic within 14 days after MI. In addition, after MI, all Snail1-positive cells were able to express periostin. These results indicate that Snail1 is mainly activated in the infarct area and is involved in de novo cardiac fibrosis after MI in mice. Thus, it is a potential molecular target in the development of drug interventions for ventricular remodeling after MI.
上皮-间充质转化(EMT)是心肌梗死后心脏纤维化的重要机制。然而,Snail1 是否参与心脏纤维化,其作为 EMT 的重要调节因子,目前仍不清楚。在本研究中,我们探讨了心肌梗死后小鼠中 Snail1 和心脏纤维化标志物-骨桥蛋白的表达模式,然后研究了心肌梗死后小鼠中 Snail1 和骨桥蛋白的共表达。结果显示,梗死区的 Snail1 和骨桥蛋白的 mRNA 和蛋白水平均显著升高。Snail1 的表达模式在心肌梗死后 14 天内呈抛物线状。此外,心肌梗死后,所有 Snail1 阳性细胞均能表达骨桥蛋白。这些结果表明,Snail1 主要在梗死区激活,并参与心肌梗死后小鼠心脏的纤维发生。因此,它是心肌梗死后心室重构药物干预发展的潜在分子靶点。