| First Author | Rosenblatt-Velin N | Year | 2012 |
| Journal | FASEB J | Volume | 26 |
| Issue | 1 | Pages | 229-39 |
| PubMed ID | 21957128 | Mgi Jnum | J:180000 |
| Mgi Id | MGI:5304978 | Doi | 10.1096/fj.11-189605 |
| Citation | Rosenblatt-Velin N, et al. (2012) Cardiac dysfunction and impaired compensatory response to pressure overload in mice deficient in stem cell antigen-1. FASEB J 26(1):229-39 |
| abstractText | Stem cell antigen-1 (Sca-1) has been used to identify cardiac stem cells in the mouse heart. To investigate the function of Sca-1 in aging and during the cardiac adaptation to stress, we used Sca-1-deficient mice. These mice developed dilated cardiomyopathy [end-diastolic left ventricular diameter at 18 wk of age: wild-type (WT) mice, 4.2 mm +/- 0.3; Sca-1-knockout (Sca-1-KO) mice, 4.6 mm +/- 0.1; ejection fraction: WT mice, 51.1 +/- 2.7%; Sca-1-KO mice, 42.9 +/- 2.7%]. Furthermore, the hearts of mice lacking Sca-1 demonstrated exacerbated susceptibility to pressure overload [ejection fraction after transaortic constriction (TAC): WT mice, 43.5 +/- 3.2%; Sca-1-KO mice, 30.8% +/- 4.0] and increased apoptosis, as shown by the 2.5-fold increase in TUNEL(+) cells in Sca-1-deficient hearts under stress. Sca-1 deficiency affected primarily the nonmyocyte cell fraction. Indeed, the number of Nkx2.5(+) nonmyocyte cells, which represent a population of cardiac precursor cells (CPCs), was 2-fold smaller in Sca-1 deficient neonatal hearts. In vitro, the ability of CPCs to differentiate into cardiomyocytes was not affected by Sca-1 deletion. In contrast, these cells demonstrated unrestricted differentiation into cardiomyocytes. Interestingly, proliferation of cardiac nonmyocyte cells in response to stress, as judged by BrdU incorporation, was higher in mice lacking Sca-1 (percentages of BrdU(+) cells in the heart after TAC: WT mice, 4.4 +/- 2.1%; Sca-1-KO mice, 19.3 +/- 4.2%). These data demonstrate the crucial role of Sca-1 in the maintenance of cardiac integrity and suggest that Sca-1 restrains spontaneous differentiation in the precursor population. The absence of Sca-1 results in uncontrolled precursor recruitment, exhaustion of the precursor pool, and cardiac dysfunction.-Rosenblatt-Velin, N., Ogay, S., Felley, A., Stanford, W. L., Pedrazzini, T. Cardiac dysfunction and impaired compensatory response to pressure overload in mice deficient in stem cell antigen-1. |
