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|本期目录/Table of Contents|

MicroRNA-214在缺氧所致心肌细胞损伤过程中的作用

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2014年第4期
页码:
393-396
栏目:
基础研究
出版日期:
2014-04-25

文章信息/Info

Title:
Role of expression changes of microRNA-214 in injury of cardiomyocytes induced by hypoxia
作者:
王 东1魏文平3王 芳2
(兰州大学第一医院:1.心内科,2.病理科 甘肃 兰州 730000;
3.兰州石化总医院呼吸科,甘肃 兰州 730060)
Author(s):
WANG Dong1 WEI Wen-ping3 WANG Fang2
(1.First Hospital, Lanzhou University, Lanzhou 730000, Gansu, China;
2.General Hospital of Lanzhou Petrochemistry, Lanzhou 730060, Gansu, China)
关键词:
MicroRNA-214低氧心肌细胞
Keywords:
microRNA-214 hypoxia cardiomyocyte
分类号:
Q522
DOI:
-
文献标识码:
A
摘要:
目的:探讨MicroRNA-214(miR-214)表达的变化与低氧诱导心肌细胞损伤的关系。方法: 实时荧光定量PCR技术检测miR-214在心肌细胞低氧损伤中表达的变化。根据培养环境和有无使用miR-214的特异性抑制剂,将心肌细胞分为常氧培养组、常氧培养+ miR-214抑制组、低氧培养组及低氧培养+miR-214抑制组。MTT比色法测定各组细胞活力,流式细胞仪(FCM)检测各组细胞的凋亡情况,酶法测定各组细胞的乳酸脱氢酶(LDH)漏出情况。结果: 低氧培养后,心肌细胞内的miR-214表达相对常氧培养的对照组有所增高(P<0.05),并呈时间依赖关系,低氧培养24 h,miR-214表达相对常氧培养的对照组可增高(1.9±0.1)倍。低氧培养会降低心肌细胞的存活率、增加心肌细胞凋亡及LDH漏出,miR-214抑制后,缺氧造成的上述损伤有所减轻。结论: miR-214的表达水平升高与低氧诱导的心肌细胞损伤有关,可能作为对抗缺氧损伤的靶点和诊断指标。
Abstract:
AIM:To investigate the relationship between cardiomyocyte injury induced by hypoxia and expression of microRNA-214 (miR-214). METHODS: The expression changes of miR-214 mRNA were detected using real- time qPCR technology. Cardiomyocytes were cultured and divided into four groups: normoxia culture group (control), normoxia culture plus miR-214 inhibitor group, hypoxia culture group, and hypoxia culture plus miR-214 inhibitor group. The proliferation of cardiomyocytes in each group was evaluated by MTT assay, apoptosis rate was analyzed by flow cytometry and the lactic dehydrogenase level was measured by enzymatic analysis. RESULTS: After hypoxia culture, a significantly high expression was detected in the cardiomyocytes compared with that in control group. Hypoxia environment inhibited the proliferation of cardiomyocytes, induced apoptosis and increased lactic dehydrogenase level, an injury marker of cardiomyocytes. However, downregulation of miR-214 caused by its specific inhibitor antagonized the cardiomyocyte injury induced by hypoxia. CONCLUSION: High expression of miR-214 is related to cardiomyocyte injury induced by hypoxia and miR-214 may be an underlying target for therapy and potential diagnostic indicator.

参考文献/References

[1]Strutyns’kyǐ RB,Nagibin VS,Strutynska NA,et al.Influence of flocalin on development of apoptosis and necrosis at anoxia-reoxygenation of culture rats neonatal cardiomyocytes[J].Fiziol Zh,2013,59(3):3-9.
[2]Chandrakala AN,Kwiatkowski P,Sai-Sudhakar CB,et al.Induction of early biomarkers in a thrombus-induced sheep model of ischemic heart failure[J].Tex Heart Inst J,2013,40(5):511-520.
[3]Zhou S,Liu Y,Prater K,et al.Roles of microRNAs in pressure overload- and ischemia-related myocardial remodeling[J].Life Sci,2013,93(23):855-862.
[4]许旭东,宋晓伟,荆 清,等.大鼠心肌肥厚过程中microRNAs的表达变化[J].蚌埠医学院学报,2010,35(12):1200-1203.
[5]程阔菊,黄 河,杜智勇,等.原代乳小鼠心肌细胞的分离培养及鉴定[J].重庆医学,2013(22):2638-2640.
[6]Zhang L,Wei S,Tang JM,et al.PEP-1-CAT protects hypoxia/reoxygenation-induced cardiomyocyte apoptosis through multiple sigaling pathways[J].J Transl Med,2013,11(9):113-121.
[7]Tang Y,Zheng J,Sun Y,et al.MicroRNA-1 regulates cardiomyocyte apoptosis by targeting Bcl-2[J].Int Heart J,2009,50(3):377-387.
[8]Ye Y,Hu Z,Lin Y,et al.Downregulation of microRNA-29 by antisense inhibitors and a PPAR-gamma agonist protects against myocardial ischaemia-reperfusion injury[J].Cardiovasc Res,2010,87(3):535-544.
[9]Ren XP,Wu J,Wang X,et al.MicroRNA-320 is involved in the regulation of cardiac ischemia/reperfusion injury by targeting heat-shock protein 20[J].Circulation,2009,119(17):2357-2366.
[10]Cheng Y,Zhu P,Yang J,et al.Ischaemic preconditioning-regulated miR-21 protects heart against ischaemia/reperfusion injury via anti-apoptosis through its target PDCD4[J].Cardiovasc Res,2010,87(3):431-439.
[11]Li DF,Tian J,Guo X,et al.Induction of microRNA-24 by HIF-1 protects against ischemic injury in rat cardiomyocytes[J].Physiol Res,2012,61(6):555-565.
[12]林述琨,王耀鹏,温吉海.miR-214对人肺癌A549细胞增殖和侵袭能力的影响[J].药品评价,2012(36):31-34.
[13]赵增仁,樊智彬,张丽静,等.结直肠癌中microRNA-214的表达及其与p53的关系[J].广东医学,2013,34(8):1213-1215.

备注/Memo

备注/Memo:
收稿日期:收稿日期:2014-01-15.通讯作者:王芳,主治医师,主要从事缺氧损伤的研究 Email:wangf_lzu@163.com 作者简介:王东,主治医师,硕士 Email:wangdong_lzu@163.com
更新日期/Last Update: 2014-05-06