Interaction with human stromal cells enhances CXCR4 expression and engraftment of cord blood Lin− CD34− cells

Objective Transplantation of hematopoietic stem cells (HSCs) is usually accomplished through intravenous injection, a complex process that requires recognition of bone marrow vasculature and migration to a supportive microenvironment. Hence, some populations of HSCs, including cord blood (CB) Lin− C...

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Veröffentlicht in:Experimental hematology 2008-09, Vol.36 (9), p.1121-1131
Hauptverfasser: Kobune, Masayoshi, Kawano, Yutaka, Takahashi, Sho, Takada, Kohichi, Murase, Kazuyuki, Iyama, Satosi, Sato, Tsutomu, Takimoto, Rishu, Niitsu, Yoshiro, Kato, Junji
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Sprache:eng
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Zusammenfassung:Objective Transplantation of hematopoietic stem cells (HSCs) is usually accomplished through intravenous injection, a complex process that requires recognition of bone marrow vasculature and migration to a supportive microenvironment. Hence, some populations of HSCs, including cord blood (CB) Lin− CD34− stem cells, do not engraft well in bone marrow (BM) of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. In this study, we examined the effect of human stromal interactions on the properties of CB Lin− CD34− cells. Materials and Methods CD34 and CXCR4 expression on fresh CB Lin− CD34− cells and CB Lin− CD34− cells cocultured with human stromal cells were analyzed. Homing activity and engraftment of these cells were assessed using NOD/SCID mice. In an attempt to identify the stromal CXCR4-inducing factor, CB Lin− CD34− cells were cocultured with a noncontact culture system in the presence of several inhibitors. Result Coculture with human stromal cells induced expression of CD34 and CXCR4 on CB Lin− CD34− cells. CXCR4 expression on CB Lin− CD34− cells was induced even in the noncontact culture condition, suggesting that this CXCR4-inducing factor is soluble. Moreover, CXCR4 induction was inhibited by the soluble Wnt inhibitor DKK1. Furthermore, these cells acquired homing activity and engrafted in the BM of NOD/SCID mice after intravenous injection. Conclusion These findings may be useful for understanding the role of stromal cells in homing and engraftment of HSCs.
ISSN:0301-472X
1873-2399
DOI:10.1016/j.exphem.2008.04.007