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Blood, 1 April 2006, Vol. 107, No. 7, pp. 2774-2776.
Prepublished online as a Blood First Edition Paper on December 8, 2005; DOI 10.1182/blood-2005-08-3210.
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Submitted August 10, 2005
Accepted November 25, 2005
Evidence for bone marrow-derived endothelial cells incorporation into perfused blood vessels in tumors
Dan G Duda, Kenneth S Cohen, Sergey V Kozin, Jean Y Perentes, Dai Fukumura, David T Scadden, and Rakesh K Jain*
Department of Radiation Oncology, E.L. Steele Laboratory for Tumor Biology, Massachusetts General Hospital, Boston, MA, USA
Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA, USA
Department of Radiation Oncology, E.L. Steele Laboratory for Tumor Biology, Massachusetts General Hospital, Boston, MA, USA; Department of Thoracic Surgery, University Hospital of Lausanne, Lausanne, Switzerland
* Corresponding author; email: jain{at}steele.mgh.harvard.edu.
Recent studies have demonstrated that the cellular contribution of the bone marrow to tumor neovascularization is highly complex. In this context, the extent to which bone marrow-derived cells incorporate as bona fide endothelial (non-hematopoietic) cells into perfused tumor vessels, or any new vessels formed postnatally (vasculogenesis), is unclear. To this end, we developed models to characterize local vessel-derived and bone marrow-derived endothelial cells (BMD-ECs). Then, we characterized the BMD-ECs based on a set of endothelial markers and morphology. Finally, we quantified their contribution to perfused blood vessels in tumors using transplanted as well as spontaneous primary and metastatic tumor models. We demonstrate that BMD-ECs incorporate in perfused tumor vessels, and that this contribution varies with organ site and mouse strain.

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