Key result
Supernatant from hypoxia-induced cardiac fibroblasts accelerated cardiac stem cell migration in vitro, an effect significantly reduced by cytokine antagonists and mediated by MMP-9.
This in vitro study demonstrates that MMP-9 secreted by hypoxic cardiac fibroblasts promotes cardiac stem cell migration, highlighting a potential mechanism for post-MI cardiac repair.
Cessation of blood supply due to myocardial infarction (MI) leads to complicated pathological alteration in the affected regions. Cardiac stem cells (CSCs) migration plays a major role in promoting recovery of cardiac function and protecting cardiomyocytes in post-MI remodeling. Despite being the most abundant cell type in the mammalian heart, cardiac fibroblasts (CFs) were underestimated in the mechanism of CSCs migration. Our objective in this study is therefore to investigate the migration related factors secreted by hypoxia CFs in vitro and the degree that they contribute to CSCs migration. We found that supernatant from hypoxia induced CFs could accelerate CSCs migration. Four migration-related cytokines were reported upregulated both in mRNA and protein levels. Upon adding antagonists of these cytokines, the number of migration cells significantly declined. When the cocktail antagonists of all above four cytokines were added, the migration cells number reduced to the minimum level. Besides, MMP-9 had an important effect on triggering CSCs migration. As shown in our results, MMP-9 induced CSCs migration and the underlying mechanism might involve TNF-α signaling which induced VEGF and MMP-9 expression.
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Guo et al. (2015) studied Myocardial infarction. Hypoxia-induced cardiac fibroblasts supernatant vs. Cytokine antagonists was evaluated on Cardiac stem cell migration. Supernatant from hypoxia-induced cardiac fibroblasts accelerated cardiac stem cell migration in vitro, an effect significantly reduced by cytokine antagonists and mediated by MMP-9.
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