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miR-21 通过调控 MMP-2 和 MMP-9 的表达对大鼠胸主动脉瘤模型的影响。

Effect of miR-21 on rat thoracic aortic aneurysm model by regulating the expressions of MMP-2 and MMP-9.

机构信息

Department of Vascular and Endovascular Surgery, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, People's Hospital of Henan University, Zhengzhou, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Jan;24(2):878-884. doi: 10.26355/eurrev_202001_20072.

DOI:10.26355/eurrev_202001_20072
PMID:32016994
Abstract

OBJECTIVE

To explore the mechanism underlying micro ribonucleic acid (miR)-21 in the invasion of rat aortic aneurysm cells in vitro by regulating matrix metalloproteinase (MMP)-2 and MMP-9.

MATERIALS AND METHODS

Rats were randomly divided into three groups: control group, model group, and miR-21 group. Real Time fluorescence quantitative Polymerase Chain Reaction (qRT-PCR) was adopted to detect the levels of miR-21 in each group of cells, transwell assay was performed to measure the effect of miR-21 on the invasion of aortic aneurysm cells. Western blotting was used to examine the expression of PTEN, which is the predicted target of miR-21 in aortic aneurysm cells, as well as the expressions of invasion-related proteases, MMP-2 and MMP-9.

RESULTS

The expression level of miR-21 in thoracic aortic aneurysm cells in model group was significantly higher than that in normal group (p<0.05), and that in miR-21 group was remarkably higher than that in model group (p<0.05). MiR-21 group had evidently more aortic aneurysm cells and stronger cell invasion ability than normal group and model group (p<0.05). In addition, the expression level of PTEN in model group was significantly higher than that in normal group (p<0.05), while that in miR-21 group notably declined compared to model group, (p<0.05). Compared with normal group and model group, the expressions of MMP-2 and MMP-9 were markedly increased in miR-21 group (p<0.05).

CONCLUSIONS

In aortic aneurysm cells of rats, miR-21 could suppress the expression of PTEN and activate MMP-2 and MMP-9 signals to promote the proliferation and migration of aortic aneurysm cells.

摘要

目的

通过调控基质金属蛋白酶(MMP)-2 和 MMP-9,探讨微小核糖核酸(miR)-21 调控大鼠主动脉瘤细胞体外侵袭的作用机制。

材料与方法

大鼠随机分为三组:对照组、模型组和 miR-21 组。采用实时荧光定量聚合酶链反应(qRT-PCR)检测各组细胞中 miR-21 的水平,Transwell 小室法检测 miR-21 对主动脉瘤细胞侵袭的影响,Western blot 检测 miR-21 靶基因 PTEN 及与侵袭相关的蛋白酶 MMP-2、MMP-9 在主动脉瘤细胞中的表达。

结果

模型组大鼠胸主动脉瘤细胞中 miR-21 的表达水平明显高于正常组(p<0.05),miR-21 组明显高于模型组(p<0.05)。miR-21 组大鼠胸主动脉瘤细胞数量明显多于正常组和模型组,细胞侵袭能力明显增强(p<0.05)。模型组大鼠主动脉瘤细胞中 PTEN 的表达水平明显高于正常组(p<0.05),miR-21 组明显低于模型组(p<0.05)。与正常组和模型组相比,miR-21 组 MMP-2 和 MMP-9 的表达明显增加(p<0.05)。

结论

在大鼠主动脉瘤细胞中,miR-21 可抑制 PTEN 的表达,激活 MMP-2 和 MMP-9 信号通路,促进主动脉瘤细胞的增殖和迁移。

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