ABSTRACT
Objective: The use of stem cells, particularly mesenchymal stem cells [MSCs], with genes and various growth factors as treatments for myocardial infarction and various other diseases is highly regarded. However these cells meet with inflammation and a hypoxic environment in the target tissue. Hence, treatment with factors that increase the resistance of these stem cells is of importance. Stem cells also can be used as carriers for gene therapy. The aim of the present research is to produce VEGF expressing MSCs. We investigate the effect of stromal derived factor 1 on MSC survival in order to use these cells in a future rat myocardial infarction model
Methods: MSCs were purified from young male rats by aspirating the cavity of femurs and tibias. After characterization, MSCs were transduced with VEGF using lipofectamine. Expression and function of VEGF was confirmed. Next, we treated MSCs with SDF1alpha at various time points. The effect of this chemokine was investigated using the LDH assay and by viable cell counts
Results: The experiments confirmed the production and function of VEGF by MSCs. The LDH levels decreased significantly in SDF1alpha treated MSCs. Cell viability increased significantly in the presence of this chemokine
Conclusion: Treatment of MSCs with the SDF1alpha chemokine has increased the survival of these cells. These MSCs are proper candidates for increasing angiogenesis and for further analysis in a rat model of myocardial infarction