Key result
Elderly CAD-derived mesenchymal stromal cells show preserved proliferative and endothelial differentiation capacity vs young donors.
Observational (n=31)
BACKGROUND: It has been questioned whether bone marrow-derived mesenchymal stromal cells (MSCs) from patients with ischemic heart disease are suitable for use in regenerative stem cell therapy. We compared MSCs from patients with chronic coronary artery disease (CAD) and MSCs from young healthy donors with respect to phenotype, proliferation and endothelial differentiation capacity. METHODS: MSCs from 16 young healthy donors and 15 elderly CAD patients were isolated, expanded by ex-vivo cultivation for two cell passages and characterized by flow cytometry, real time PCR and angiogenesis assay. RESULTS: MSCs from healthy donors and CAD patients expressed the same surface markers and had similar proliferation capacity. In both groups VEGF-stimulation significantly increased the expression of the endothelial genes thrombospondin 1, Tie-2 and von Willebrand Factor and induced the capacity to form ring structures on extracellular matrix. DISCUSSION: MSCs from young healthy donors and CAD patients proliferate equally well, express the same surface markers and increase in endothelial gene expression and ring structure formation capacity in the angiogenesis assay upon VEGF-stimulation. MSCs from CAD patients do not seem to be inferior to MSCs from young healthy donors thus indicating that autologous MSCs may be suitable for cell therapy in CAD patients.
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Friis et al. (2011) conducted an observational in Severe chronic coronary artery disease (n=31). Mesenchymal stromal cells (MSCs) from elderly CAD patients vs. MSCs from young healthy donors was evaluated on Phenotype, proliferation, and endothelial differentiation capacity. Mesenchymal stromal cells from elderly CAD patients demonstrated similar proliferation, surface marker expression, and endothelial differentiation capacity compared to MSCs from young healthy donors.
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