Li Liang, Chen Qiang, Feng Chao, Jin Yongping, Xia Shudong
Department of Cardiology, The Fourth Affiliated Hospital Zhejiang University School of Medicine, Yiwu, 322000 Zhejiang China.
3 Biotech. 2019 Jul;9(7):285. doi: 10.1007/s13205-019-1812-7. Epub 2019 Jun 25.
In the present study, aberrant expression of trinucleotide repeat-containing gene 6a (TNRC6a) and miR-21 was noted and documented in rat myocardial infarction. Briefly, Sprague-Dawley rat model was used for the development of myocardial infarction. Experiments such as histological analysis were carried out to confirm the histopathology of the myocardial infarction. The expression profile of TNRC6a and miR-21 was identified by using quantitative real-time PCR. In addition, immunoblotting was performed to validate the expression profile of TNRC6a and phosphatase and tensin homolog (PTEN). The histological analysis confirmed the progress of myocardial infarction in rat model. As the disease progresses, the protein TNRC6a expresses abnormally which in turn up-regulates the miR-21 after 3rd and 5th week of infarction. Interestingly, miR-21 binds with its specific target genes PTEN and thereby degrades the target mRNA; as a result, its expression was down-regulated progressively and paved the development of myocardial infarction. The present study concludes that the aberrant expression of TNRC6a and miR-21 was documented during myocardial infarction. These findings play an important role in the diagnosis as well as pave a way for the development of drug targets for treating myocardial infarction.
在本研究中,在大鼠心肌梗死中发现并记录了含三核苷酸重复序列基因6a(TNRC6a)和miR-21的异常表达。简要来说,采用斯普拉格-道利大鼠模型建立心肌梗死模型。进行了组织学分析等实验以确认心肌梗死的组织病理学变化。通过定量实时PCR确定TNRC6a和miR-21的表达谱。此外,进行免疫印迹以验证TNRC6a和磷酸酶及张力蛋白同源物(PTEN)的表达谱。组织学分析证实了大鼠模型中心肌梗死的进展。随着疾病进展,蛋白TNRC6a异常表达,进而在梗死第3周和第5周后上调miR-21。有趣的是,miR-21与其特异性靶基因PTEN结合,从而降解靶mRNA;结果,PTEN的表达逐渐下调,促进了心肌梗死的发展。本研究得出结论,在心肌梗死期间记录到了TNRC6a和miR-21的异常表达。这些发现对诊断具有重要作用,也为开发治疗心肌梗死的药物靶点铺平了道路。