Novel evidence of the increase in angiogenic factor plasma levels after lineage-negative stem/progenitor cell intracoronary infusion in patients with acute myocardial infarction

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Abstract

Cell therapy raises hope to reduce the harmful effects of acute myocardial ischemia. Stem and progenitor cells (SPCs) may be a valuable source of trophic factors. In this study, we assessed the plasma levels of selected trophic factors in patients undergoing application of autologous bone marrow (BM)-derived, lineage-negative (Lin− ) stem/progenitor cells into the coronary artery in the acute phase of myocardial infarction. The study group consisted of 15 patients with acute myocardial infarction (AMI) who underwent percutaneous revascularization and, afterwards, Lin− stem/progenitor cell administration into the infarct-related artery. The control group consisted of 19 patients. BM Lin− cells were isolated using immunomagnetic methods. Peripheral blood was collected on day 0, 2, 4, and 7 and after the first and third month to assess the concentration of selected trophic factors using multiplex fluorescent bead-based immunoassays. We found in the Lin− group that several angiogenic trophic factors (vascular endothelial growth factor, Angiopoietin-1, basic fibroblast growth factor, platelet-derived growth factor-aa) plasma level significantly increased to the 4th day after myocardial infarction. In parallel, we noticed a tendency where the plasma levels of the brain-derived neurotrophic factor were increased in the Lin– group. The obtained results suggest that the administered SPCs may be a valuable source of angiogenic trophic factors for damaged myocardium, although this observation requires further in-depth studies.

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Baumert, B., Przybycień, K., Paczkowska, E., Kotowski, M., Pius-Sadowska, E., Safranow, K., … Machaliński, B. (2019). Novel evidence of the increase in angiogenic factor plasma levels after lineage-negative stem/progenitor cell intracoronary infusion in patients with acute myocardial infarction. International Journal of Molecular Sciences, 20(13). https://doi.org/10.3390/ijms20133330

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