TY - JOUR
T1 - Differentiation, Metabolism, and Cardioprotective Secretory Functions of Human Cardiac Stromal Cells from Ischemic and Endocarditis Patients
AU - Nguyen, Helen
AU - Hsu, Chuan Chih
AU - Meeson, Annette
AU - Oldershaw, Rachel
AU - Richardson, Gavin
AU - Czosseck, Andreas
AU - Lundy, David J.
N1 - Publisher Copyright:
© Mary Ann Liebert, Inc.
PY - 2024
Y1 - 2024
N2 - 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.
AB - 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.
KW - coronary artery bypass graft
KW - differentiation
KW - human cardiac cells
KW - mesenchymal stromal cell
KW - senescence
KW - Cardiovascular diseases
KW - Genetic Engineering
KW - Biotechnology
KW - Regenerative medicine
KW - Medicine
KW - Surgery & Diagnosis
KW - Mesenchymal stem cell
KW - Myocardial infarction
KW - Myocardial ischemia
KW - Stem cell engineering
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=85198929527&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85198929527&partnerID=8YFLogxK
U2 - 10.1089/scd.2024.0103
DO - 10.1089/scd.2024.0103
M3 - Article
C2 - 38940748
AN - SCOPUS:85198929527
SN - 1547-3287
VL - 33
SP - 484
EP - 495
JO - Stem Cells and Development
JF - Stem Cells and Development
IS - 17-18
ER -