miR-21 Reduces Hydrogen Peroxide-Induced Apoptosis in c-kit(+) Cardiac Stem Cells In Vitro through PTEN/PI3K/Akt Signaling.
miR-21 Reduces Hydrogen Peroxide-Induced Apoptosis in c-kit(+) Cardiac Stem Cells In Vitro through PTEN/PI3K/Akt Signaling.
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miR-21 通过 PTEN/PI3K/Akt 信号传导减少体外 c-kit( ) 心脏干细胞中过氧化氢诱导的细胞凋亡
DOI:
10.1155/2016/5389181
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发表时间:
2016
影响因子:
--
通讯作者:
Shi B
中科院分区:
文献类型:
--
作者:
Deng W;Wang Y;Long X;Zhao R;Wang Z;Liu Z;Cao S;Shi B
The low survival rate of cardiac stem cells (CSCs) in the infarcted myocardium hampers cell therapy for ischemic cardiomyopathy. MicroRNA-21 (miR-21) and one of its target proteins, PTEN, contribute to the survival and proliferation of many cell types, but their prosurvival effects in c-kit+ CSC remain unclear. Thus, we hypothesized that miR-21 reduces hydrogen peroxide- (H2O2-) induced apoptosis in c-kit+ CSC and estimated the contribution of PTEN/PI3K/Akt signaling to this oxidative circumstance. miR-21 mimics efficiently reduced H2O2-induced apoptosis in c-kit+ CSC, as evidenced by the downregulation of the proapoptosis proteins caspase-3 and Bax and upregulation of the antiapoptotic Bcl-2. In addition, the gain of function of miR-21 in c-kit+ CSC downregulated the protein level of PTEN although its mRNA level changed slightly; in the meantime, miR-21 overexpression also increased phospho-Akt (p-Akt). The antiapoptotic effects of miR-21 were comparable with Phen (bpV), the selective inhibitor of PTEN, while miR-21 inhibitor or PI3K's inhibitor LY294002 efficiently attenuated the antiapoptotic effect of miR-21. Taken together, these results indicate that the anti-H2O2-induced apoptosis effect of miR-21 in c-kit+ CSC is contributed by PTEN/PI3K/Akt signaling. miR-21 could be a potential molecule to facilitate the c-kit+ CSC therapy in ischemic myocardium.
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DOI:
10.1074/jbc.m113.495531
发表时间:
2014-02-07
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Di Bernardini E;Campagnolo P;Margariti A;Zampetaki A;Karamariti E;Hu Y;Xu Q
通讯作者:
Xu Q
影响因子:
37.8
作者:
Bolli R;Tang XL;Sanganalmath SK;Rimoldi O;Mosna F;Abdel-Latif A;Jneid H;Rota M;Leri A;Kajstura J
通讯作者:
Kajstura J
影响因子:
9.5
作者:
Hong KU;Li QH;Guo Y;Patton NS;Moktar A;Bhatnagar A;Bolli R
通讯作者:
Bolli R
影响因子:
2.7
作者:
Cao S;Liu Y;Wang H;Mao X;Chen J;Liu J;Xia Z;Zhang L;Liu X;Yu T
通讯作者:
Yu T
影响因子:
--
作者:
Ciuffreda, Ludovica;Falcone, Italia;Milella, Michele
通讯作者:
Milella, Michele