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. Author manuscript; available in PMC: 2018 Feb 1.
Published in final edited form as: Nature. 2017 May 17;545(7655):439–445. doi: 10.1038/nature22326

Figure 2. Conditional Fgrs expression supports long-term primary and secondary HSPC engraftment.

Figure 2

a, Transplantation schema. b, Lineage contribution to Gr1+CD11b+ and Gr1CD11b+ myeloid cells, B220+ B cells, CD3+CD4+ T cells, and CD3+CD8+ T cells at week 20 after primary transplant in the peripheral blood of WBM control transplant recipients (blue circles) or rEC-HSPC recipients (green circles), Boxplot and whiskers represent median, 25th and 75th percentile, mean is represented by + sign (n = 4 independent conversion experiments run in technical triplicates for each condition); two-tailed unpaired t-test. c, Lineage contribution to Gr1+CD11b+ and Gr1CD11b+ myeloid cells, B220+ B cells, CD3+CD4+ T cells, and CD3+CD8+ T cells at week 20 after secondary transplant in the peripheral blood of WBM control transplant (blue circles) or rEC-HSPC (green circles), Boxplot and whiskers represent median, 25th and 75th percentile, mean is represented by + sign (n = 4 independent conversion experiment run in technical triplicates for each conditions); two-tailed unpaired t-test. d, Relative representation of LKS and LKS-SLAM cells at week 20 after primary transplant for WBM transplant recipients (blue circles) or rEC-HSPC recipients (green circles). e, Relative representation of LKS and LKS-SLAM cells at week 20 after secondary transplant for WBM transplant recipients (blue circles) or rEC-HSPC recipients (green circles). Boxplot and whiskers represent median, 25th and 75th percentile, mean is represented by + sign (n = 4 independent conversion experiment run in technical triplicates for each conditions); two-tailed unpaired t-test