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Fibrogenic Potential of PW1/Peg3 Expressing Cardiac Stem Cells.
Yaniz-Galende, Elisa; Roux, Maguelonne; Nadaud, Sophie; Mougenot, Nathalie; Bouvet, Marion; Claude, Olivier; Lebreton, Guillaume; Blanc, Catherine; Pinet, Florence; Atassi, Fabrice; Perret, Claire; Dierick, France; Dussaud, Sébastien; Leprince, Pascal; Trégouët, David-Alexandre; Marazzi, Giovanna; Sassoon, David; Hulot, Jean-Sébastien.
Afiliación
  • Yaniz-Galende E; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Roux M; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Nadaud S; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Mougenot N; Sorbonne-Universités, UPMC, Plate forme d'Expérimentation Coeur Muscles Vaisseaux, Paris, France.
  • Bouvet M; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Claude O; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Lebreton G; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Blanc C; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Pinet F; INSERM U1167, Université de Lille, Institut Pasteur de Lille, Fédération Hospitalo-Universitaire Remodeling in Valvulopathy and Heart Failure, Lille, France.
  • Atassi F; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Perret C; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Dierick F; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Dussaud S; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Leprince P; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Trégouët DA; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Marazzi G; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Sassoon D; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France.
  • Hulot JS; Sorbonne-Universités, Université Pierre-et-Marie-Curie (UPMC), INSERM UMRS_1166, Institute of Cardiometabolism and Nutrition, Paris, France. Electronic address: jean-sebastien.hulot@aphp.fr.
J Am Coll Cardiol ; 70(6): 728-741, 2017 Aug 08.
Article en En | MEDLINE | ID: mdl-28774379
ABSTRACT

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 PW1nLacZ+/- 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN / Función Ventricular Izquierda / Remodelación Ventricular / Factores de Transcripción de Tipo Kruppel / Células Madre Mesenquimatosas / Infarto del Miocardio / Miocardio Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Am Coll Cardiol Año: 2017 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN / Función Ventricular Izquierda / Remodelación Ventricular / Factores de Transcripción de Tipo Kruppel / Células Madre Mesenquimatosas / Infarto del Miocardio / Miocardio Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Am Coll Cardiol Año: 2017 Tipo del documento: Article País de afiliación: Francia
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