JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY | 卷:70 |
Fibrogenic Potential of PW1/Peg3 Expressing Cardiac Stem Cells | |
Article | |
Yaniz-Galende, Elisa1  Roux, Maguelonne1  Nadaud, Sophie1  Mougenot, Nathalie2  Bouvet, Marion1  Claude, Olivier1  Lebreton, Guillaume1  Blanc, Catherine1  Pinet, Florence3  Atassi, Fabrice1  Perret, Claire1  Dierick, France1  Dussaud, Sebastien1  Leprince, Pascal1  Tregouit, David-Alexandre1  Marazzi, Giovanna1  Sassoon, David1  Hulot, Jean-Sebastien1  | |
[1] UPMC, Sorbonne Univ, INSERM UMRS 1166, Inst Cardiometab & Nutr, Paris, France | |
[2] UPMC, Sorbonne Univ, Plate Forme Expt Coeur Muscles Vaisseaux, Paris, France | |
[3] Univ Lille, Inst Pasteur Lille, INSERM U1167, Lille, France | |
关键词: cardiac stem cells; fibrosis; ischemic cardiomyopathy; myocardial infarction; | |
DOI : 10.1016/j.jacc.2017.06.010 | |
来源: Elsevier | |
【 摘 要 】
BACKGROUND Pw1 gene expression is a marker of adult stem cells in a wide range of tissues. PW1-expressing cells are detected in the heart but are not well characterized. OBJECTIVES The authors characterized cardiac PW1-expressing cells and their cell fate potentials in normal hearts and during cardiac remodeling following myocardial infarction (MI). METHODS A human cardiac sample was obtained from a patient presenting with reduced left ventricular (LV) function following a recent MI. The authors used the PW1(nLacZ+/-) reporter mouse to identify, track, isolate, and characterize PW1-expressing cells in the LV myocardium in normal and ischemic conditions 7 days after complete ligature of the left anterior descending coronary artery. RESULTS In both human and mouse ischemic hearts, PW1 expression was found in cells that were mainly located in the infarct and border zones. Isolated cardiac resident PW1(+) cells form colonies and have the potential to differentiate into multiple cardiac and mesenchymal lineages, with preferential differentiation into fibroblast-like cells but not into cardiomyocytes. Lineage-tracing experiments revealed that PW1(+) cells differentiated into fibroblasts post-MI. Although the expression of c-Kit and PW1 showed little overlap in normal hearts, a marked increase in cells coexpressing both markers was observed in ischemic hearts (0.1 +/- 0.0% in control vs. 5.7 +/- 1.2% in MI; p < 0.001). In contrast to the small proportion of c-Kit(+)/PW1(-) cells that showed cardiogenic potential, c-Kit(+)/PW1(+) cells were fibrogenic. CONCLUSIONS This study demonstrated the existence of a novel population of resident adult cardiac stem cells expressing PW1(+) and their involvement in fibrotic remodeling after MI. (C) 2017 by the American College of Cardiology Foundation.
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