Key result
Stem cell factor (SCF) increased cardiac stem cell migration in a concentration-dependent manner via the activation of PI3K/AKT/MMP-2/-9 signaling.
Why the study?
Does stem cell factor (SCF) increase cardiac stem cell migration through PI3K/AKT and MMP-2/-9 signaling?
Does stem cell factor (SCF) increase cardiac stem cell migration through PI3K/AKT and MMP-2/-9 signaling?
SCF promotes the migration of adult rat cardiac stem cells in vitro via the activation of the PI3K/AKT/MMP-2/-9 signaling pathway, providing mechanistic insights for stem cell therapy post-myocardial infarction.
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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Guo et al. (2014) studied Myocardial infarction (in vitro model context). Stem cell factor (SCF) vs. Control medium or SCF with inhibitors (LY294002, SCF antibody) was evaluated on Cardiac stem cell migration and MMP-2/-9 expression (p=<0.05). Stem cell factor (SCF) increased cardiac stem cell migration in a concentration-dependent manner via the activation of PI3K/AKT/MMP-2/-9 signaling.
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