4.7 Article

Mobilization of Bone Marrow-Derived Oct-4+ SSEA-4+ Very Small Embryonic-Like Stem Cells in Patients With Acute Myocardial Infarction

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Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2008.09.029

Keywords

very small embryonic-like stem cells; pluripotent stem cells; acute myocardial infarction; mobilization

Funding

  1. National Institutes of Health [R01 CA10628101]
  2. Polish Ministry of Science and Higher Education [PBZ-KBN-099/P05/2003, 0651/P01/2007/32, 2422/P01/2007/32]
  3. European Vascular Genomics Network

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Objectives This study sought to assess of the mobilization of nonhematopoietic very small embryonic-like stem cells (VSELs) in acute myocardial infarction (MI). Background Acute MI induces mobilization of bone marrow stem cells. Recently, a rare population of VSELs, expressing markers of embryonic pluripotent stem cells (PSCs), was identified in adult murine bone marrow and human umbilical cord blood. Methods Thirty-one patients with acute MI and 30 healthy subjects were enrolled. Blood was sampled on admission, after 24 h, and 5 days later. Erythrocytes were lysed and lin(-)CD45(-) VSELs were isolated using a live cell sorting system (FACSAria, Beckton Dickinson, San Jose, California). Results In healthy subjects the median number of circulating VSELs was very low (median 0.8 [ range 0 to 1.3]) cells/mu l. In acute MI, VSELs were mobilized early (median 2.7 [range 0.2 to 3.9] cells/mu l; p < 0.001) and remained elevated after 24 h and 5 days (median 4.7 [range 0.2 to 6.4] cells/mu l; p < 0.003, and median 2.6 [ range 0.3 to 3.6] cells/mu l; p < 0.03, respectively). The mobilization of VSEL was significantly reduced in patients older than 50 years and with diabetes in comparison with younger and nondiabetic patients. Circulating VSELs were small (7 to 8 mu m) and enriched in the messenger ribonucleic acid of PSC markers (Oct-4, Nanog), cardiac lineage (GATA-4, Nkx2.5/Csx, MEF2C), and endothelial (VE-cadherin) markers. The presence of PSC markers (Oct-4, SSEA-4) and the chemokine receptor CXCR4 in circulating VSELs was confirmed at the protein level by immunofluorescent staining and ImageStream system (Amnis Corporation, Seattle, Washington) analysis. Conclusions Acute MI induced mobilization of VSELs expressing pluripotent markers, early cardiac and endothelial markers, and chemokine receptor CXCR4. (J Am Coll Cardiol 2009; 53:1-9) (c) 2009 by the American College of Cardiology Foundation

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