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. 2018 Dec 7;9:340. doi: 10.1186/s13287-018-1074-z

Fig. 3.

Fig. 3

MEIS2 deletion impairs early hematopoiesis of hESCs. a Representative morphology of “cobblestone-like” cells generated from WT, MEIS2+/−, and MEIS2−/− hESCs at day 7 of hematopoietic differentiation. The “cobblestone-like” cells were indicated by orange arrows. Scale bar, 50 μm. b Immunofluorescence of WT, MEIS2+/−, and MEIS2−/− hESCs with antibody against CD43 (red) at day 7 of hematopoietic differentiation. Nuclei were stained with DAPI (blue). Scale bars, 50 μm. c Flow cytometry analysis of CD43+ hematopoietic precursors generated from WT, MEIS2+/−, and MEIS2−/− hESCs at day 7 of differentiation. d Flow cytometry analysis of CD45+ hematopoietic cells generated from WT, MEIS2+/−, and MEIS2−/− hESCs at day 11 of differentiation. e The total number of colonies derived from WT, MEIS2+/−, and MEIS2−/− hESCs (left). The proportion of BFU-E, CFU-E, CFU-GM, and CFU-GEMM in total colonies. Results are shown as means ± SEM (n = 3). NS not significant; *P < 0.05, **P < 0.01, and ***P < 0.001