Abstract
Although clinical benefit can be achieved after cardiac transplantation of adult c-kit+ or cardiosphere-derived cells for myocardial repair, these stem cells lack the regenerative capacity unique to neonatal cardiovascular stem cells. Unraveling the molecular basis for this age-related discrepancy in function could potentially transform cardiovascular stem cell transplantation. In this report, clonal populations of human neonatal and adult cardiovascular progenitor cells were isolated and characterized, revealing the existence of a novel subpopulation of endogenous cardiovascular stem cells that persist throughout life and co-express both c-kit and isl1. Epigenetic profiling identified 41 microRNAs whose expression was significantly altered with age in phenotypically-matched clones. These differences were correlated with reduced proliferation and a limited capacity to invade in response to growth factor stimulation, despite high levels of growth factor receptor on progenitors isolated from adults. Further understanding of these differences may provide novel therapeutic targets to enhance cardiovascular regenerative capacity. © 2013 Fuentes et al.
| Original language | English |
|---|---|
| Article number | e77464 |
| Journal | PLOS One |
| Volume | 8 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 28 2013 |
ASJC Scopus Subject Areas
- General Biochemistry,Genetics and Molecular Biology
- General Agricultural and Biological Sciences
- General
Keywords
- MicroRNAs/genetics
- Age Factors
- Signal Transduction
- Epigenesis, Genetic
- Humans
- Cells, Cultured
- Proto-Oncogene Proteins c-kit/genetics
- Gene Expression Profiling
- Transcription Factors/genetics
- Receptors, Growth Factor/genetics
- Stem Cell Transplantation
- Adult Stem Cells/cytology
- Intercellular Signaling Peptides and Proteins/pharmacology
- Gene Expression Regulation, Developmental
- Myocardium/metabolism
- LIM-Homeodomain Proteins/genetics
- Regeneration/genetics
- Adult
- Cell Differentiation
- Cell Proliferation/drug effects
- Infant, Newborn
- Myocytes, Cardiac/cytology
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