MiR-194-3p对成纤维细胞的增殖作用研究  被引量:4

The effect of miR-194-3p on the proliferation of fibroblasts

在线阅读下载全文

作  者:徐志山 常鹏[2] 郭冰玉[2] 回蔷[2] 马书丹 李伟[2] 陶凯 XU Zhi-shan;CHANG Peng;GUO Bing-yu;HU;MA Shu-dan;LI Wei;TAO Kai(The General Hospital of Shenyang Military Region, Postgraduate Training Base of Jinzhou Medical University, Shenyang 110016, China)

机构地区:[1]锦州医科大学沈阳军区总医院研究生培养基地,辽宁沈阳110016 [2]沈阳军区总医院整形外科,辽宁沈阳110016

出  处:《中国美容整形外科杂志》2018年第6期362-365,共4页Chinese Journal of Aesthetic and Plastic Surgery

摘  要:目的 研究瘢痕疙瘩中miR-194-3p对成纤维细胞增殖作用的影响,为瘢痕疙瘩的治疗提供理论基础。方法 对瘢痕疙瘩标本应用基因芯片筛选出与正常组织差异表达的miRNA,并通过real-time PCR技术来验证miR-194-3p表达;采用Western-blot和real-time PCR分析miR-194-3p对其靶蛋白RUNX2的调节作用。在成纤维细胞中过表达或抑制miR-194-3p后,通过MTT实验观察其对成纤维细胞增殖的作用。通过Western-blot和real-time PCR探讨其对RUNX2及其增殖相关蛋白CDK4的调控作用。结果 miR-194-3p在瘢痕疙瘩中呈下调表达,其能够抑制RUNX2的表达;miR-194-3p可以通过抑制增殖相关蛋白CDK4来抑制成纤维细胞的增殖。结论 miR-194-3p可以抑制瘢痕疙瘩成纤维细胞的增殖。Objective To analyze the effects of miR-194-3p on the proliferation of fibroblasts in keloids, and provide a theoretical basis for the treatment of keloids. Methods The differential expression of miRNAs with normal tissue was screened by microarray analysis on keloids. Real-time PCR technique was used to verify the expression of miR-194-3p. Western blot and real-time PCR were used to analyze the regulatory effect of miR-194-3p on its target protein RUNX2. After overexpression or inhibition of miR-194-3p in fibroblasts, the proliferation of fibroblasts was observed by MTT experiment. Western blot and real time PCR were used to investigate the regulation of RUNX2 and CDK4, its proliferation-related protein. Results The expression of miR-194-3p was down-regulated in keloids, and it was able to inhibit the expression of RUNX2. MiR-194-3p was able to inhibit the proliferation of fibroblasts by inhibiting CDK4, the proliferation-related protein. Conclusion MiR-194-3p can inhibit the proliferation of keloid fibroblasts.

关 键 词:瘢痕疙瘩 miR-194-3p 成纤维细胞 增殖 

分 类 号:R622[医药卫生—整形外科]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象