[1]吕爱婷,冯迎军,孙琪青,等.病毒性心肌炎患儿外周血中微小RNA-98的表达及其对凋亡相关蛋白/凋亡相关蛋白配体表达的影响[J].新乡医学院学报,2018,35(10):889-894.[doi:10.7683/xxyxyxb.2018.10.010]
 LYU Ai-ting,FENG Ying-jun,SUN Qi-qing,et al.Expression of micro RNA-98 in peripheral blood of children with viral myocarditis and its effect on the expression of factor associated suicide/factor associated suicide ligand[J].Journal of Xinxiang Medical University,2018,35(10):889-894.[doi:10.7683/xxyxyxb.2018.10.010]
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病毒性心肌炎患儿外周血中微小RNA-98的表达及其对凋亡相关蛋白/凋亡相关蛋白配体表达的影响
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《新乡医学院学报》[ISSN:1004-7239/CN:41-1186/R]

卷:
35
期数:
2018年10
页码:
889-894
栏目:
临床研究
出版日期:
2018-10-05

文章信息/Info

Title:
Expression of micro RNA-98 in peripheral blood of children with viral myocarditis and its effect on the expression of factor associated suicide/factor associated suicide ligand
作者:
吕爱婷冯迎军孙琪青候维纳
(郑州大学附属儿童医院血管内科,河南 郑州 450000)
Author(s):
LYU Ai-tingFENG Ying-junSUN Qi-qingHOU Wei-na
(Department of Cardiovascular Medicine,the Children′s Hospital Affiliated to Zhengzhou University,Zhengzhou 450000,Henan Province,China)
关键词:
微小RNA病毒性心肌炎心肌细胞凋亡相关蛋白
Keywords:
micro RNAviral myocarditiscardiac myocytefactor associated suicide
分类号:
R542.2+1
DOI:
10.7683/xxyxyxb.2018.10.010
文献标志码:
A
摘要:
目的 探讨病毒性心肌炎(VM)患儿外周血中微小RNA-98(miR-98)的水平及其对凋亡相关蛋白(Fas)/凋亡相关蛋白配体(FasL)表达的影响。方法 选择2015年9月至2017年7月郑州大学附属儿童医院收治的VM患儿62例作为VM组,根据左心室射血分数(LVEF)及心肌肌钙蛋白(cTnI)水平将VM组患儿分为轻度组(n=38)和重度组(n=24),另选择56例健康儿童作为对照组。采用实时荧光定量聚合酶链反应(qRT-PCR)测定3组受试者外周血中miR-98、Fas、FasL mRNA表达水平,Western blot检测Fas、FasL蛋白表达水平。体外培养人心肌细胞(HCM)、H9C2心肌细胞至占培养皿底面积80%时,将细胞分为空白组(不做任何处理)、阴性转染组(无意义序列转染至细胞内)和miR-98转染组(miR-98 siRNA转染至细胞内)。采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐法检测3组细胞培养12、24、48、72 h时细胞增殖情况;平板细胞克隆形成实验检测细胞克隆形成情况;流式细胞仪检测细胞凋亡情况。结果 VM组患儿外周血中miR-98相对表达量低于对照组(P<0.05),Fas、FasL mRNA相对表达量高于对照组(P<0.05),重度组患儿外周血中miR-98相对表达量低于轻度组,Fas、FasL mRNA相对表达量高于轻度组(P<0.05)。VM组患儿外周血中Fas、FasL蛋白相对表达量高于对照组(P<0.05),重度组患儿外周血中Fas、FasL蛋白相对表达量高于轻度组(P<0.05)。VM组患儿外周血中miR-98与Fas、FasL呈显著负相关(r=-516、-463,P<0.05)。miR-98转染组HCM、H9C2心肌细胞抑制率在各时间点均高于空白组和阴性转染组(P<0.05)。miR-98转染组HCM、H9C2心肌细胞克隆数量和miR-98相对表达量低于空白组和阴性转染组(P<0.05),HCM、H9C2细胞凋亡率及HCM、H9C2心肌细胞中Fas、FasL蛋白相对表达量高于空白组和阴性转染组(P<0.05)。结论 miR-98在VM患儿外周血中表达水平下降,其可能是通过调节Fas/FasL基因在心肌细胞中的表达来参与心肌细胞损伤和凋亡。
Abstract:
Objective To explore the level of micro RNA-98(miR-98) in peripheral blood of children with viral myocarditis(VM) and its effect on the expression of factor associated suicide(Fas)/factor associated suicide ligand(FasL).Methods Sixty-two VM children in the Children′s Hospital Affiliated of Zhengzhou University from September 2015 to July 2017 were selected as VM group,the children in VM group were divided into mild group(n=38) and severe group(n=24) according to left ventricular ejection fraction(LVEF) and cardiac troponin(cTnI) levels.And 56 healthy children were selected as control group.The expressions of miR-98 and Fas,FasL mRNA in peripheral blood of children in the three groups were detected by quantitative real time polymerase chain reaction(qRT-PCR) and the expressions of Fas,FasL protein were detected by Western blot.The human cardiac myocytes(HCM),H9C2 cells were cultured in petri dish and proliferated to the bottom area of the dish 80%.Then the cells were divided into blank group (without any treatment),negative transfection group (control sequence transfected into cells) and miR-98 transfection group (miR-98 transfected into cells).The cell proliferation was detected by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide assay at 12,24,48 and 72 h after cultured;the colony formation was detected by plate cell clone formation assay;the cell apoptosis was detected by flow cytometry.Results The expression of miR-98 mRNA in the peripheral blood of children in the VM group was significantly lower than that in the control group(P<0.05),but the expressions of Fas,FasL mRNA were significantly higher than those in the control group(P<0.05);the expression of miR-98 in peripheral blood of children of them in the severe group was lower than that in the mild group,and the expression of Fas,FasL mRNA in peripheral blood of children in the severe group was higher than that in the mild group(P<0.05).The expression of Fas and FasL protein in the peripheral blood of children in the VM group was significantly higher than that in the control group(P<0.05),and the expression of Fas and FasL protein in the severe group was significantly higher than that in the mild group(P<0.05).There was a significant negative correlation between miR-98 and Fas,FasL in peripheral blood of children in the VM group(r=-516,-463;P<0.05).The inhibition rates of HCM and H9C2 cells in miR-98 transfection group were significantly higher than those in blank group and negative transfection group at each time point(P<0.05).The number of cell colonies and the expression of miR-98 in HCM and H9C2 cells in the miR-98 transfection group were significantly lower than those in the blank group and the negative transfection group(P<0.05).The apoptotic rate of HCM and H9C2 cells and the expression of Fas,FasL protein in HCM and H9C2 cells in the miR-98 transfection group were significantly higher than those in the blank group and the negative transfection group(P<0.05).Conclusion The expression level of miR-98 in peripheral blood of children with VM is decreased.It may be involve in the injury and apoptosis of cardiac myocytes by regulating the expression of Fas/FasL gene in cardiac myocytes.

参考文献/References:

[1] 钱玉洁,杨作成.病毒性心肌炎与细胞死亡机制[J].中华实用儿科临床杂志,2018,33(1):18-20.
[2] 张淑芹,刘志屹,戴璐,等.长春地区病毒性心肌炎患儿柯萨奇B组病毒感染的流行病学分析[J].中国妇幼保健,2014,29(1):75-77.
[3] 王焰斌,崔刚,王小雷,等.Fas/FasL信号通路在乌司他丁后处理减轻CPB下心脏瓣膜置换术患者心肌细胞凋亡中的作用[J].中华麻醉学杂志,2014,34(8):940-943.
[4] HOOGEN P V D,AKKER F V D,DEDDENS J C,et al.Heart failure in chronic myocarditis:a role for microRNAs[J].Curr Genomics,2015,16(2):88-92.
[5] 中华医学会儿科学分会心血管学组.病毒性心肌炎诊断标准(修订草案)[J].中华儿科杂志,2000,38(2):75-78.
[6] 裴丽,张军平.病毒性心肌炎诊断的研究进展[J].中华实用儿科临床杂志,2011,26(10):795-797.
[7] 成捷,刘新光,熊兴东.miRNA,lncRNA与心血管疾病[J].中国生物化学与分子生物学报,2014,30(4):328-335.
[8] 姜晖,陈霞霞,王金艳.川芎嗪对柯萨奇病毒B3感染小鼠心肌细胞凋亡的影响研究[J].中华医院感染学杂志,2014,24(13):3121-3123.
[9] ZHU W,YANG L,SHAN H,et al.MicroRNA expression analysis:clinical advantage of propranolol,reveals key microRNAs in myocardial infarction[J].PLoS One,2011,6(2):14736-14742.
[10] 石晓凤,韦小未,朱建兵,等.microRNA 与冠状动脉粥样硬化性心脏病的相关性研究[J].中华临床医师杂志:电子版,2013,7(24):39- 42.DOI:10.3877/cma.j.issn.1674-0785.2013.24.013.
[11] HUO Y,CHU Y,GUO L,et al.Cortisol is associated with low frequency of interleukin 10-producing B cells in patients with atherosclerosis[J].Cell Biochem Funct,2017,35(3):178-185.
[12] 陈铁龙,祝光礼,赫小龙,等.冠心合剂减少大鼠心肌梗死边缘区凋亡及对Fas、FasL、Caspase-8、Caspase-3蛋白表达的影响[J].中华中医药学刊,2013,31(11):2453-2455.
[13] 高学东,胡科,魏虎.心脏干细胞对心肌细胞凋亡的保护机制[J].中国组织工程研究,2016,20(36):5405-5411.
[14] 姜志梅,郭津,王亚军,等.丙戊酸钠诱导孤独症模型大鼠大脑组织中Fas/FasL表达的意义[J].中华实用儿科临床杂志,2014,29(20):1575-1577.
[15] 陈星如,高卫萍.针刺对干眼兔泪腺形态学及泪腺上皮细胞凋亡相关基因蛋白表达的影响[J].眼科新进展,2017,37(3):210-214.
[16] 梅花,任少敏,傅亮.小儿病毒性心肌炎与Fas/Fasl介导的外周血淋巴细胞凋亡的关系[J].中国小儿急救医学,2011,18(4):320-322.
[17] HUANG T F,WU X H,WANG X,et al.Fas-FasL expression and myocardial cell apoptosis in patients with viral myocarditis[J].Genet Mol Res,2016,15(2):1249-1253.
[18] SUN C,LIU H,GUO J,et al.MicroRNA-98 negatively regulates myocardial infarction-induced apoptosis by down-regulating Fas and caspase-3[J].Sci Rep,2017,7(1):7460-7466.
[19] WU T,CHEN J,FAN L,et al.Effects of Shenqi Fuzheng injection on Fas/FasL protein expression levels in the cardiomyocytes of a mouse model of viral myocarditis[J].Exp Ther Med,2016,11(5):1839-1844.
[20] ZHANG B Y,ZHAO Z,JIN Z.Expression of miR-98 in myocarditis and its influence on transcription of the Fas/FasL gene pair[J].Genet Mol Res,2016,15(2):627632-62763.

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更新日期/Last Update: 2018-10-05