Cardiac Progenitor Cells and Adipocyte Stem Cells from Same Patients Exhibit In Vitro Functional Differences.
Anthony Soonseng Yee-GohAtsushi YamauchiIsabelle van HoutJayanthi Bellae PapannaraoRamanen SugunesegranDominic ParryPhilip DavisRajesh G KatarePublished in: International journal of molecular sciences (2022)
Cardiac progenitor cells (CPCs) and adipocyte stem cells (ASCs) are widely tested for their efficacy in repairing the diseased heart with varying results. However, no study has directly compared the functional efficacy of CPCs and ASCs collected from the same patient. CPCs and ASCs were isolated from the right atrial appendage and epicardial adipose tissue of the same patients, using explant culture. The flow cytometry analysis confirmed that both the cell types express common mesenchymal stem cells markers CD90 and CD105. ASCs, in addition, expressed CD29 and CD73. The wound-healing assay demonstrated that CPCs migrate faster to cover the wound area. Both cell types were resistant to hypoxia-induced cell death when exposed to hypoxia and serum deprivation; however, the ASCs showed increased proliferation. Conditioned medium (CM) collected after culturing serum-deprived CPCs and ASCs showed differential secretion patterns, with ASC CM showing an increased IGF-1 level, while CPC CM showed an increased FGF level. Only CPC CM reduced hypoxia-induced apoptosis in AC-16 human ventricular cardiomyocytes, while vascular network formation by endothelial cells was comparable between CPC and ASC CM. In conclusion, ASCs and CPCs exhibit differential characteristics within the same patient, and in vitro studies showed that CPCs have marginally superior functional efficacy.
Keyphrases
- endothelial cells
- stem cells
- adipose tissue
- end stage renal disease
- induced apoptosis
- mesenchymal stem cells
- cell death
- cell therapy
- newly diagnosed
- ejection fraction
- flow cytometry
- chronic kidney disease
- left ventricular
- heart failure
- signaling pathway
- prognostic factors
- single cell
- oxidative stress
- atrial fibrillation
- type diabetes
- endoplasmic reticulum stress
- nk cells
- metabolic syndrome
- left atrial
- vascular endothelial growth factor
- pi k akt
- umbilical cord
- induced pluripotent stem cells