SCF increases cardiac stem cell migration through PI3K/AKT and MMP-2/-9 signaling

被引:52
作者
Guo, Junli [1 ]
Jie, Wei [2 ]
Shen, Zhihua [2 ]
Li, Mengsen [3 ]
Lan, Youling [1 ]
Kong, Yueqiong [1 ]
Guo, Shaoli [1 ]
Li, Tianfa [1 ]
Zheng, Shaojiang [1 ]
机构
[1] Hainan Med Coll, Affiliated Hosp, Cardiovasc Inst, Haikou 571199, Peoples R China
[2] Guangdong Med Coll, Sch Basic Med Sci, Dept Pathol, Zhanjiang 524023, Peoples R China
[3] Hainan Med Coll, Hainan Prov Key Lab Carcinogenesis & Intervent, Haikou 571199, Peoples R China
基金
中国国家自然科学基金;
关键词
cardiac stem cells; stem cell factor (SCF)/c-Kit system; PI3K/AKT signaling; cell migration; matrix metalloproteinase-2; matrix metalloproteinase-9; RANDOMIZED PHASE-1 TRIAL; MYOCARDIAL-INFARCTION; ISCHEMIC CARDIOMYOPATHY; VENTRICULAR-FUNCTION; HEART REGENERATION; PROGENITOR CELLS; P38; MAPK; ACTIVATION; THERAPY; CARDIOPROTECTION;
D O I
10.3892/ijmm.2014.1773
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
The transplantation of cardiac stem cells (CSCs) is thought to be responsible for improving the performance of injured heart induced by myocardial infarction (MI). However, the mechanisms involved in the migration of activated CSCs post-MI remain to be clarified. In this study, CSCs were isolated from rat hearts and a cellular migration assay was performed using a 24-well Transwell system. Stem cell factor (SCF) induced CSC migration in a concentration-dependent manner, which could be blocked with an SCF antibody as well as a PI3K/AKT inhibitor, LY294002. Moreover, SCF induced the expression and activity of matrix metalloproteinase (MMP)-2 and MMP-9 in a concentration- and time-dependent manner, as measured by quantitative RT-PCR, western blot analysis and gelatin zymography. Results of western blot analysis revealed phosphorylated AKT was markedly increased in SCF-treated CSCs and that inhibition of SCF/c-Kit signaling or phospho-AKT activity significantly attenuated the SCF-induced expression of MMP-2 and MMP-9. Thus, our results showed that SCF partially mediated CSC migration via the activation of PI3K/AKT/MMP-2/-9 signaling.
引用
收藏
页码:112 / 118
页数:7
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