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首页> 外文期刊>Journal of nanoscience and nanotechnology >Investigate the Effect of miR-22 on the Apoptosis of Coronary Heart Disease Cells Through the Wnt-1 Pathway Based on Nano-Silica-Induced Rat Models
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Investigate the Effect of miR-22 on the Apoptosis of Coronary Heart Disease Cells Through the Wnt-1 Pathway Based on Nano-Silica-Induced Rat Models

机译:基于纳米二氧化硅诱导的大鼠大鼠模型,探讨MiR-22对冠心病细胞凋亡的影响

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摘要

In this paper, by examining the toxicity of nano-silica to coronary heart disease cells, we explored the apoptosis of rat myocardial cells induced by nano-silica, and explored the effect of apoptosis on cells during the process of myocardial cytotoxicity induced by nano-silica. Thisarticle selects rat cardiomyocytes as the research object and conducts a group control experiment. A control group is set up with cells that are not stained with nano-silica. Different concentrations of nanosilica suspensions are applied to rat cells and detected by CCK-8 method. Cell survivalrate after exposure to different concentrations of cells is used to determine the most stable exposure time and concentration. We used flow cytometry to detect intracellular reactive oxygen species and apoptotic rates, and used Western Blot to detect the expression of proteins that affectapoptosis. Finally, we investigated the effect of the Wnt signaling pathway on coronary heart disease. The Wnt signaling pathway regulates the development of the heart and blood vessels. In the treatment of cardiovascular disease, this pathway will be activated again to play a regulatory role.We conclude that nano-silica can induce cytotoxicity in rat myocardial cells through the Wnt-1 pathway, and nanosilica can induce myocardial cell apoptosis through the Wnt-1 pathway.
机译:本文通过检测纳米二氧化硅对冠心病细胞的毒性,探讨了纳米二氧化硅诱导大鼠心肌细胞凋亡,以及纳米二氧化硅诱导心肌细胞毒性过程中细胞凋亡对细胞的影响。本文以大鼠心肌细胞为研究对象,进行了分组对照实验。对照组由未被纳米二氧化硅染色的细胞组成。将不同浓度的纳米二氧化硅悬浮液应用于大鼠细胞,并用CCK-8法检测。暴露于不同浓度细胞后的细胞存活率用于确定最稳定的暴露时间和浓度。我们使用流式细胞术检测细胞内活性氧和凋亡率,并使用westernblot检测影响细胞凋亡的蛋白质的表达。最后,我们研究了Wnt信号通路在冠心病中的作用。Wnt信号通路调节心脏和血管的发育。在心血管疾病的治疗中,该通路将再次被激活,发挥调节作用。我们得出结论,纳米二氧化硅可以通过Wnt-1途径诱导大鼠心肌细胞的细胞毒性,纳米二氧化硅可以通过Wnt-1途径诱导心肌细胞凋亡。

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