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THE STEM CELL NICHE

The Role of the Donor in the Repair of the Marrow Vascular Niche Following Hematopoietic Stem Cell Transplant

^aUniversity of Florida Program in Stem Cell Biology and Regenerative Medicine,
^bDepartment of Pediatrics, and
^cBlood and Marrow Transplant Program, University of Florida Health Science Center, Gainesville, Florida, USA

Key Words. Niche • Marrow sinusoids • Hematopoietic stem cells • Repair

Correspondence: William B. Slayton, M.D., UFHSC Box 100296, Gainesville, Florida 32610, USA. Telephone: 352-392-5633; Fax: 352-392-8725; e-mail: slaytwb{at}peds.ufl.edu

Received March 9, 2007; accepted for publication July 20, 2007.
First published online in STEM CELLS EXPRESS   July 26, 2007.



Bone marrow sinusoids maintain homeostasis between developing hematopoietic cells and the circulation, and they provide niches for hematopoietic progenitors. Sinusoids are damaged by chemotherapy and radiation. Hematopoietic stem cells (HSCs) have been shown to produce endothelial progenitor cells that contribute to the repair of damaged blood vessels. Because HSCs home to the marrow during bone marrow transplant, these cells may play a role in repair of marrow sinusoids. Here, we explore the role of donor HSCs in the repair of damaged sinusoids following hematopoietic stem cell transplant. We used three methods to test this role: (a) expression of platelet endothelial cell adhesion molecule to identify endothelial progenitors and the presence of the Y chromosome to identify male donor cells in female recipients; (b) presence of the Y chromosome to identify male donor cells in female recipients, and expression of the panendothelial marker mouse endothelial cell antigen-32 to identify sinusoidal endothelium; and (c) use of Tie-2/green fluorescent protein mice as donors or recipients and presence of Dil-Ac-LDL to identify sinusoids. We found that sinusoids were predominantly host-derived posttransplant. Donor cells spread along the marrow vasculature early post-transplant in a pattern that matched stromal-derived factor-1 expression. Furthermore, these engrafting progenitors were positioned to provide physical support, as well as growth and survival signals in the form of vascular-endothelial growth factor-A. Occasionally, donor cells provide cellular "patches" in the damaged sinusoids, although this occurred at a low level compared with hematopoietic engraftment. Donor support for the repair of the marrow vascular niche may be a critical first step of hematopoietic engraftment.

Disclosure of potential conflicts of interest is found at the end of this article.