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miR-25对P19细胞向心肌细胞分化的影响及机制

李连冲

中国组织工程研究2016,Vol.20Issue(11):1584-1590,7.
中国组织工程研究2016,Vol.20Issue(11):1584-1590,7.DOI:10.3969/j.issn.2095-4344.2016.11.010

miR-25对P19细胞向心肌细胞分化的影响及机制

Effect of miR-25 on the differentiation of P19 cells into cardiomyocytes and its mechanism

李连冲1

作者信息

  • 1. 南阳医学高等专科学校第一附属医院心血管外科,河南省南阳市 473000
  • 折叠

摘要

Abstract

BACKGROUND:Previous studies have found that the expression level of miR-25 in differentiated P19 cels is significantly lower than that in undifferentiated P19 cels. However, the effect of miR-25 on cardiomyogenesis and the relevant mechanism remain unclear. <br> OBJECTIVE: To explore the effect and mechanism of miR-25 on the differentiation of P19 cels into cardiomyocytes. <br> METHODS:P19 cels were cultured and differentiated into cardiomyocytesin vitro. The expression of miR-25 in differentiated and undifferentiated P19 cels was detected by real-time PCR. miR-25-overexpressing P19 cels were constructed by lipofection transfection, and were used to investigate the effect of miR-25 on the differentiation of P19 cels into cardiomyocytes. MicroRNA target analysis tools were used to explore potential targets of miR-25, and dual luciferase reporter assay was used to identify whether the 3’UTR of Pax3 mRNA was a binding target of miR-25. In addition, we transfected P19 cels with Pax3 shRNAs to silence the expression of Pax3, and investigated the effect of Pax3 on the differentiation of P19 cels into cardiomyocytes. <br> RESULTS AND CONCLUSION: Expression level of miR-25 in differentiated P19 cels was obviously down-regulated compared with that in undifferentiated P19 cels. miR-25 overexpression promoted the differentiation of P19 cels into cardiomyocytes. By target prediction analysis, we confirmed that Pax3 was a potential target gene of miR-25. Luciferase assay further confirmed that miR-25 targeted Pax3 directly. Moreover, knockdown of Pax3 promoted the differentiation of P19 cels into cardiomyocytes. Taken together, miR-25 promotes the differentiation of P19 cels into cardiomyocytes by targeting Pax3. These findings offer new clues and theoretical basis for cardiomyogenesis and prevention and cure of congenital heart disease.

关键词

组织构建/组织工程/心肌细胞/miR-25/P19细胞/分化/先天性心脏病/Pax3

Key words

Myocytes, Cardiac/MicroRNAs/Cel Differentiation

分类

医药卫生

引用本文复制引用

李连冲..miR-25对P19细胞向心肌细胞分化的影响及机制[J].中国组织工程研究,2016,20(11):1584-1590,7.

中国组织工程研究

OA北大核心CSTPCD

2095-4344

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