期刊文献+

沉默Dnmt1基因表达诱导大鼠骨髓间充质干细胞向心肌样细胞分化 被引量:3

Silencing of the Dnmt1 Gene Induces Differentiation of Rat Mesenchymal Stem Cells to Cardiac Muscle-like Cells
下载PDF
导出
摘要 骨髓间充质干细胞(MSCs)具有向心肌样细胞分化的潜能.本室前期研究发现,MSCs在体外经DNA甲基转移酶(Dnmt)抑制剂5-氮胞苷诱导可分化为心肌样细胞.本研究证明,沉默DNA甲基化转移酶1(Dnmt1)基因表达,可诱导大鼠MSCs向心肌样细胞分化.本文采用表达Dnmt1 siRNA慢病毒感染MSCs,沉默Dnmt1表达.DNA甲基化分析显示,随着沉默Dnmt1时间延长(7-28 d),Gata-4基因上游DNA调控序列的Cp G甲基化水平明显降低,而Gata-4 mRNA的转录水平明显上调,说明敲减Dnmt1表达导致Gata-4基因激活.蛋白质印迹和/或免疫细胞化学揭示,与对照组比较,心肌相关基因MHC和c Tn T表达上调,而骨髓干细胞标志物CD90和CD29随转染时间延长表达下调.同时,实时定量PCR显示,心肌早期发育调控基因Nkx2.5 mRNA水平与Gata-4 mRNA相同,随表达Dnmt1 siRNA的慢病毒感染而上调.上述结果提示,敲减Dnmt1可降低心肌发育调控基因Gata-4启动子Cp G岛的甲基化水平,上调Gata-4基因的表达,诱导骨髓间充质干细胞向心肌样分化. Mesenchymal stem cells(MSCs) have been shown to be the potential to differentiate to cardiac muscle-like cells.We have previously demonstrated that exposure of MSCs to the Dnmt inhibitors5-azacytidine(5-aza-CR) may induce the differentiation of MSCs to cardiac muscle-like cells.Herein,we demonstrated that silencing Dnmt1 expression induced differentiation of rat MSCs to cardiac musclelike cells.First,Dnmt1 siRNA expressing lentivirus was constructed and infected MSCs to silence Dnmt1 expression.Methylation PCR assay showed that after different time of infection,the methylation levels of the Cp G island in the Gata-4 upstream sequence were markedly declined,while the levels of Gata-4mRNA were up-regulated,indicating the activation of the Gata-4 gene under the condition of Dnmt1 knockdown.Western blotting and/or immunocytochemistry revealed that in comparison with the control,the levels of cardiac MHC and c Tn T proteins were up-regulated,whereas the CD90 and CD29 proteins as MSCs markers were down-regulated in Dnmt-1 silenced MSCs.Furthermore,real-time quantitative-PCR(RT-q PCR) showed that the early cardiac muscle regulatory gene Nkx2.5 as well as Gata-4 was upregulated.These data suggest that silencing of Dnmt1 may induce the expression of the Gata-4 gene by reducing the levels of the Cp G island methylation in its promoter,thereby to promote MSC differentiation to cardiac-muscle related cells.
作者 蒋昌科 龚放
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2015年第4期408-413,共6页 Chinese Journal of Biochemistry and Molecular Biology
基金 重庆市卫生局重点项目(No.2011-1-082)~~
关键词 骨髓间充质干细胞 心肌 分化 DNA甲基转移酶1 mesenchymal stem cells(MSCs) cardiac muscle differentiation DNA methyltransferase 1
  • 相关文献

参考文献21

  • 1Patil R, Kumar B M, Lee W J,et al. Muhilineage potential and proteomic profiling of human dental stem ceils derived from a single donor[J]. Exp Cell Res, 2014, 320(1): 92-107.
  • 2Pisano F, Mura M, Cervio E, et al. Overexpression of growth factors to improve cardiac differentiation of human mesenchymal stem cells derived from the amniotic membrane[ J ]. Eur Heart J, 2013, 34(suppl 1 ) : 5692.
  • 3Mura M, Pisano F, Malpasso G, et al. Novel IRES-based lentivirus co-expressing IGFI and BMP2 enhances both cardiomyogenesis and cytoprotection of bone marrow-derived mesenchymal stem cells[J]. Eur Heart J, 2013, 34(supp[ 1 ) : 1473.
  • 4ArmifiOn A, Gandia C, Bartual M, et al. Cardiac differentiation is driven by NKX2. 5 and GATA4 nuclear translocation in tissue- specific, mesenchymal stem cells[ J]. Stem Cells Dev, 2009, 18 (6) : 907-918.
  • 5廖礼强,张晓刚,史若飞,王丁琼,汤为学.微血管内皮细胞诱导骨髓间充质干细胞向心肌样分化及其移植的可行性[J].中国组织工程研究与临床康复,2009,13(40):7811-7816. 被引量:4
  • 6郭茂娟,范英昌,徐秀梅,赵旭.5-氮胞苷诱导骨髓间充质干细胞向心肌细胞的分化[J].中国组织工程研究与临床康复,2007,11(46):9238-9241. 被引量:9
  • 7Tomita S, Li R K, Weisel R D, et al. Autologous transplantation of bone marrow cells improves damaged heart function [ J ]. Circulation, 1999, 100( 19 suppl ): 247-256.
  • 8Antonitsis P, loannidou-Papagiannaki E, Kaidoglou AKaidoglou A, et al. In vitro cardiomyogenic differentiation of adult human bone marrow mesenchymal stem cells. The rfie of 5- azaeytidine [J]. Interact Cardiovasc Thorac Surg, 2007, 6(5): 593-597.
  • 9张文,田杰,江德勤,张蕾,朱静,陈沅.骨髓间充质干细胞体外分化为心肌样细胞相关调控基因的时序表达[J].中华心血管病杂志,2004,32(11):1004-1008. 被引量:25
  • 10Robert M F, Morin S, Beaulieu N, et al. DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cells[J]. Nat Genet, 2003, 33(1): 61-65.

二级参考文献10

共引文献35

同被引文献40

引证文献3

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部