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Brief Reviews |
From the Departments of Pediatrics and of Molecular and Cellular Biology (K.K.H.), Center for Cell & Gene Therapy and Childrens Nutrition Research Center, Baylor College of Medicine, Houston, Tex; and the Department of Pediatrics (D.A.I., M.C.Y.), Herman B. Wells Center for Pediatric Research, Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis.
Correspondence to Karen K. Hirschi, Departments of Pediatrics and of Molecular and Cellular Biology, Center for Cell & Gene Therapy and Childrens Nutrition Research Center, Baylor College of Medicine, Houston, TX 77030. E-mail khirschi@bcm.tmc.edu
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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The endothelium has become a particularly scrutinized cell population with the recognition that these cells may play important roles in maintaining vascular homeostasis and in the pathogenesis of a variety of diseases.2 Although it has been known for several decades that some shed or extruded endothelial cells enter the circulation as apparent contaminants in the human blood stream,3 only more recent technologies have permitted the identification of not only senescent sloughed endothelial cells,4 but also endothelial progenitor cells (EPCs), which have been purported to represent a normal component of the formed elements of circulating blood5 and play roles in disease pathogenesis.6–9 Most citations refer to an article published in 1997 in which Asahara and colleagues isolated, characterized, and examined the in vivo function of putative EPCs from human peripheral blood as a major impetus for generating
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