Differentiation, Metabolism, and Cardioprotective Secretory Functions of Human Cardiac Stromal Cells from Ischemic and Endocarditis Patients.
Helen NguyenChuan-Chih HsuAnnette MeesonRachel OldershawGavin RichardsonAndreas CzosseckDavid J LundyPublished in: Stem cells and development (2024)
This study investigates the characteristics of cardiac mesenchymal stem cell-like cells (CMSCLCs) isolated from the right atrial appendage of human donors with ischemia and a young patient with endocarditis (NE-CMSCLCs). Typical CMSCLCs from ischemic heart patients were derived from coronary artery bypass grafting procedures and compared against bone marrow mesenchymal stromal cells (BM-MSCs). NE-CMSCLCs had a normal immunophenotype, but exhibited enhanced osteogenic differentiation potential, rapid proliferation, reduced senescence, reduced glycolysis, and lower reactive oxygen species generation after oxidative stress compared with typical ischemic CMSCLCs. These differences suggest a unique functional status of NE-CMSCLCs, influenced by the donor health condition. Despite large variances in their paracrine secretome, NE-CMSCLCs retained therapeutic potential, as indicated by their ability to protect hypoxia/reoxygenation-injured human cardiomyocytes, albeit less effectively than typical CMSCLCs. This research describes a unique cell phenotype and underscores the importance of donor health status in the therapeutic efficacy of autologous cardiac cell therapy.
Keyphrases
- bone marrow
- cell therapy
- mesenchymal stem cells
- endothelial cells
- end stage renal disease
- coronary artery bypass grafting
- oxidative stress
- chronic kidney disease
- ejection fraction
- reactive oxygen species
- stem cells
- heart failure
- healthcare
- ischemia reperfusion injury
- coronary artery disease
- prognostic factors
- mental health
- dna damage
- patient reported outcomes
- pluripotent stem cells
- brain injury
- middle aged
- heat stress