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Blood, 15 March 2007, Vol. 109, No. 6, pp. 2365-2372. Prepublished online as a Blood First Edition Paper on November 9, 2006; DOI 10.1182/blood-2006-05-022640.
HEMATOPOIESIS Transplantation of vascular endothelial cells mediates the hematopoietic recovery and survival of lethally irradiated mice1 Division of Cellular Therapy, Department of Medicine, Duke University Medical Center, Durgam, NC; 2 Department of Ophthalmology, Duke University Medical Center, Durham, NC Flk-1+ endothelial progenitors contribute critically to the definitive onset of hematopoiesis during embryogenesis. Recent studies have suggested that adult sources of endothelial cells also possess hematopoietic activity. In this study, we sought to determine whether transplantation of primary vascular endothelial cells (ECs) could enhance the hematopoietic recovery and survival of irradiated mice. C57Bl6 mice were exposed to sublethal and lethal doses of irradiation and were subsequently given transplants of either primary murine brainderived ECs (MBECs) or fetal blood-derived ECs (FBECs). Mice that received a transplant with MBECs alone demonstrated accelerated BM cellular recovery, radioprotection of BM c-kit+sca-1lin progenitors and enhanced regeneration of c-kit+sca-1+lin (KSL) stem/progenitor cells following irradiation compared with controls. MBEC transplantation also facilitated the recovery of circulating white blood cell and platelet counts following radiation exposure. Remarkably, 57% of mice that received a transplant with MBECs alone survived long term following 1050 cGy exposure, which was 100% lethal in control mice. FBEC transplantation was also associated with increased survival compared with controls, although these mice did not survive in the long term. These data suggest that reestablishment of endothelial cell activity can improve the hematopoietic recovery and survival of irradiated mice.
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