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Blood, 15 January 2005, Vol. 105, No. 2, pp. 679-681.
Prepublished online as a Blood First Edition Paper on September 9, 2004; DOI 10.1182/blood-2004-05-1906.
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Submitted May 18, 2004
Accepted August 27, 2004
Vascular Leukocytes Contribute to Tumor Vascularization
Jose R Conejo-Garcia, Ronald J Buckanovich, Fabian Benencia, Maria C Courreges, Stephen C Rubin, Richard G Carroll, and George Coukos*
Center for Research in Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, USA
Division of Gynecologic Oncology, University of Pennsylvania, Philadelphia, PA, USA
Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA, USA
Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA, USA; Center for Research in Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, USA; Division of Gynecologic Oncology, University of Pennsylvania, Philadelphia, PA, USA
* Corresponding author; email: gcks{at}mail.med.upenn.edu.
There is no proof that hematopoetic cells contribute significantly to vasculogenesis in postnatal life. Here we report a novel leukocyte subset within ovarian carcinoma which co-expresses endothelial and dendritic cell markers. FACS analysis identified a high frequency of VE-cadherin+CD45+ leukocytes (39% of host cells) in 10 of 10 solid tumors evaluated. This population represented <1% of non-tumor cells in ascites and peripheral blood. At the protein level, more than 86% of these cells expressed the endothelial markers P1H12, CD34 and CD31, and leukocyte markers CD11c and MHC-II. At the mRNA level, we detected TEM1, TEM7, and Thy-1, specific markers of angiogenic endothelium. Finally, this population has the capacity to generate functional blood vessels in vivo. Because of their mixed phenotype, we named this population "vascular leukocytes" (VLCs). Our data provide an important link between hematopoetic endothelial precursors and vascular development in postnatal life and a possible novel therapeutic target.

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