CXCR4‐Transgene Expression Significantly Improves Marrow Engraftment of Cultured Hematopoietic Stem Cells

Sebastian Brenner(National Institutes of Health), Narda Whiting‐Theobald(National Institutes of Health), Toshinao Kawai(Jikei University School of Medicine), Gilda F. Linton(National Institute of Allergy and Infectious Diseases), Andrew G. Rudikoff(National Institute of Allergy and Infectious Diseases), Uimook Choi(National Institutes of Health), Martin Ryser(University Hospital Carl Gustav Carus), Philip M. Murphy(National Institutes of Health), Joan M. G. Sechler(National Institute of Allergy and Infectious Diseases), Harry L. Malech(National Institute of Allergy and Infectious Diseases)
Stem Cells
December 1, 2004
Cited by 118Open Access
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Abstract

Hematopoietic stem cells (HSCs) lose marrow reconstitution potential during ex vivo culture. HSC migration to stromal cell-derived factor (SDF)-1 (CXCL12) correlates with CXC chemokine receptor 4 (CXCR4) expression and marrow engraftment. We demonstrate that mobilized human CD34+ peripheral blood stem cells (CD34+ PBSCs) lose CXCR4 expression during prolonged culture. We transduced CD34+ PBSCs with retrovirus vector encoding human CXCR4 and achieved 18-fold more CXCR4 expression in over 87% of CD34+ cells. CXCR4-transduced cells yielded increased calcium flux and up to a 10-fold increase in migration to SDF-1. Six-day cultured CXCR4-transduced cells demonstrated significant engraftment in nonobese diabetic/severe combined immunodeficient mice under conditions in which control transduced cells resulted in low or no engraftment. We conclude that transduction-mediated overexpression of CXCR4 significantly improves marrow engraftment of cultured PBSCs.


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