Open AccessThe Role of the Donor in the Repair of the Marrow Vascular Niche Following Hematopoietic Stem Cell Transplant
Author(s) -
Slayton William B.,
Li XiaoMiao,
Butler Jason,
Guthrie Steven M.,
Jorgensen Marda L.,
Wingard John R.,
Scott Edward W.
Publication year - 2007
Publication title -
stem cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.159
H-Index - 229
eISSN - 1549-4918
pISSN - 1066-5099
DOI - 10.1634/stemcells.2007-0158
Subject(s) - biology , stem cell , bone marrow , haematopoiesis , endothelial stem cell , progenitor cell , stromal cell , hematopoietic stem cell , immunology , microbiology and biotechnology , cd34 , cancer research , genetics , in vitro
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.