Caloric restriction does not alter effects of aging in cardiac side population cells

• Published in: AGE 2011-09, Vol.33 (3), p.351-361
• Main Authors: Mulligan, Jacob D., Schmuck, Eric G., Ertel, Rebecca L., Brellenthin, Angie G., Bauwens, Jake D., Saupe, Kurt W.
• Format: Article
• Language: English
• Subjects: Age; Aging; Aging - physiology; Analysis; Animals; Biomedical and Life Sciences; Caloric Restriction; Cardiomyocytes; Cell Biology; Cell cycle; Cell Proliferation; Cellular Senescence; Diet; Flow cytometry; Gene expression; Geriatrics/Gerontology; Heart; Heart - physiology; Life Sciences; Male; Mice; Mice, Inbred C57BL; Models, Animal; Molecular Medicine; Myocardium - cytology; Population; Senescence; Smooth muscle; Stains & staining; Stem cells; Stem Cells - physiology; Studies; Telomerase
• ISSN: 0161-9152; 2509-2715; 1574-4647; 2509-2723
• DOI: 10.1007/s11357-010-9188-y

The aged heart displays a loss of cardiomyocyte number and function, possibly due to the senescence and decreased regenerative potential that has been observed in some cardiac progenitor cells. An important cardiac progenitor that has not been studied in the context of aging is the cardiac side population (CSP) cell. To address this, flow cytometry-assisted cell sorting was used to isolate CSP cells from adult (6–10 months old) and aged (24–32 months old) C57Bl/6 mice that were fed either a control diet or an anti-aging diet (caloric restriction, CR). Aging caused a 2.3-fold increase in the total number of CSP cells and a 3.2-fold increase in the cardiomyogenic sca1 + /CD31 − subpopulation. Aging did not affect markers of proliferation or senescence, including telomerase activity and expression of cell cycle genes, in sca1 + /CD31 − CSP cells. In contrast, the aged cells had reduced expression of genes associated with differentiation, including smooth muscle actin and cardiac muscle actin (5.1- and 3.2-fold, respectively). None of these age effects were altered by CR diet. Therefore, it appears that the manner in which CSP cells age is distinct from the aging of post-mitotic tissue (and perhaps other progenitor cells) that can often be attenuated by CR.