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SCF increases cardiac stem cell migration through PI3K/AKT and MMP-2/-9 signaling
Author(s) -
Junli Guo,
Wei Jie,
Zhihua Shen,
Mengsen Li,
You-Ling Lan,
Yue-Qiong Kong,
Shaoli Guo,
Tianfa Li,
Shaojiang Zheng
Publication year - 2014
Publication title -
international journal of molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.048
H-Index - 90
eISSN - 1791-244X
pISSN - 1107-3756
DOI - 10.3892/ijmm.2014.1773
Subject(s) - protein kinase b , western blot , pi3k/akt/mtor pathway , stem cell factor , ly294002 , chemistry , stem cell , matrix metalloproteinase , cell migration , microbiology and biotechnology , phosphorylation , signal transduction , cancer research , biology , cell , biochemistry , haematopoiesis , gene
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.

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