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. 2018 Jan 23;4:4. doi: 10.1038/s41421-017-0004-z

Fig. 3. Loss of Asxl1 in the BM niche alters HSC/HPC pool.

Fig. 3

a Frequencies of LT-HSC, ST-HSC, and MPP cell populations in BM reconstituted CD45.1+/LSK cells of OsxCre;Asxl1fl/fl recipients are shown (n = 3 mice per genotype). b Absolute numbers of LT-HSCs, ST-HSCs, and MPP cells from Asxl1fl/fl and OsxCre;Asxl1fl/fl recipients are shown (n = 3 mice per genotype). c Flow cytometric analyses of CMP, GMP, and MEP populations in the reconstituted CD45.1+/LKS cells from BM of representative Asxl1fl/fl and OsxCre;Asxl1fl/fl recipients. d Quantification of the percent CMP, GMP, and MEP populations in BM reconstituted CD45.1+/LKS cells of OsxCre;Asxl1fl/fl recipients are shown (n = 3 mice per genotype). e Flow cytometric analysis of Gr1+/Mac1+ cell populations in PB of representative Asxl1fl/fl and OsxCre;Asxl1fl/fl recipients. f, g Quantification of Gr1+/Mac1+ cell populations in PB (f) and spleen (g) shows increased myeloid cells in OsxCre;Asxl1fl/fl recipients (n = 4 mice per genotype). Data represent mean ± s.e.m., ns, not significant, *P < 0.05, **P < 0.01