Cxcr2−/− HSCs show a reduction in engraftment in primary and secondary BM transplantation assays. (A) Experimental layout for CD45.2+ HSCs from WT or Cxcr2−/− mice (n = 3 per strain) transplanted into irradiated CD45.1+ recipients (n = 6). (B) Graph showing engraftment ability of CD45.2+ WT or Cxcr2−/− HSC after 24 hours from transplant in CD45.1+ recipients. (C) Graph showing chimerism between CD45.2+ and CD45.1+ cells. (D) Engraftment was analyzed in the blood every 4 weeks posttransplant up to 16 weeks. Data are presented as the mean percentage of CD45.2+ cells within the PB. (E) After the primary recipients were sacrificed, CD45.2+ LSK cells were transplanted into irradiated recipients. Engraftment was analyzed in the blood every 4 weeks posttransplant up to 16 weeks. (F) Percentage of CD45.2+ cells was analyzed in different BM populations after 16 weeks from primary transplant, and compared between WT and Cxcr2−/− mice. Statistical analysis was performed using an unpaired two-tailed Student t test. All error bars indicate SEM of the mean (*P < .05; **P < .01; ***P < .001) (n = 6).