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Abcg2-Labeled Cells Contribute to Different Cell Populations in the Embryonic and Adult Heart.
Doyle, Michelle J; Maher, Travis J; Li, Qinglu; Garry, Mary G; Sorrentino, Brian P; Martin, Cindy M.
Afiliación
  • Doyle MJ; 1 Department of Medicine, Lillehei Heart Institute, University of Minnesota , Minneapolis, Minnesota.
  • Maher TJ; 1 Department of Medicine, Lillehei Heart Institute, University of Minnesota , Minneapolis, Minnesota.
  • Li Q; 1 Department of Medicine, Lillehei Heart Institute, University of Minnesota , Minneapolis, Minnesota.
  • Garry MG; 1 Department of Medicine, Lillehei Heart Institute, University of Minnesota , Minneapolis, Minnesota.
  • Sorrentino BP; 2 Department of Experimental Hematology, St. Jude Children's Research Hospital , Memphis, Tennessee.
  • Martin CM; 1 Department of Medicine, Lillehei Heart Institute, University of Minnesota , Minneapolis, Minnesota.
Stem Cells Dev ; 25(3): 277-84, 2016 Feb 01.
Article en En | MEDLINE | ID: mdl-26573225
ATP-binding cassette transporter subfamily G member 2 (Abcg2)-expressing cardiac-side population cells have been identified in the developing and adult heart, although the role they play in mammalian heart growth and regeneration remains unclear. In this study, we use genetic lineage tracing to follow the cell fate of Abcg2-expressing cells in the embryonic and adult heart. During cardiac embryogenesis, the Abcg2 lineage gives rise to multiple cardiovascular cell types, including cardiomyocytes, endothelial cells, and vascular smooth muscle cells. This capacity for Abcg2-expressing cells to contribute to cardiomyocytes decreases rapidly during the postnatal period. We further tested the role of the Abcg2 lineage following myocardial injury. One month following ischemia reperfusion injury, Abcg2-expressing cells contributed significantly to the endothelial cell lineage, however, there was no contribution to regenerated cardiomyocytes. Furthermore, consistent with previous results showing that Abcg2 plays an important cytoprotective role during oxidative stress, we show an increase in Abcg2 labeling of the vasculature, a decrease in the scar area, and a moderate improvement in cardiac function following myocardial injury. We have uncovered a difference in the capacity of Abcg2-expressing cells to generate the cardiovascular lineages during embryogenesis, postnatal growth, and cardiac regeneration.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Daño por Reperfusión Miocárdica / Transportadoras de Casetes de Unión a ATP / Linaje de la Célula / Miocitos Cardíacos / Corazón Fetal Límite: Animals Idioma: En Revista: Stem Cells Dev Asunto de la revista: HEMATOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Daño por Reperfusión Miocárdica / Transportadoras de Casetes de Unión a ATP / Linaje de la Célula / Miocitos Cardíacos / Corazón Fetal Límite: Animals Idioma: En Revista: Stem Cells Dev Asunto de la revista: HEMATOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos