Figure 2
Figure 2. Analysis of the cell-intrinsic effects of Srf deletion. (A) Experimental outline of transplantation experiments. Srfflx/flx;Mx1-Cre whole BM cells (CD45.2, 4 × 106 totals) were transplanted into 6-week-old lethally irradiated wild-type littermate recipients (CD45.1). The recipients were treated or not with pIpC 4 weeks postengraftment to induce Srf-deletion exclusively in hematopoietic cells and not in BM stromal cells. Mice were analyzed 5 weeks after Cre induction. (B) Table of the hematologic parameters, BM cellularity, and spleen weight. Values shown are mean ± SEM (n = 7 per group, ***P < .001 by Mann-Whitney test). (C) Cell autonomous expansion of the LSK and MP compartments in recipient mice treated or not with pIpC. (n = 7 per group, *P < .05). (D) BM (2 × 104), spleen (2 × 105) and PB (5 × 105) cells of recipient mice treated or not with pIpC were plated in methylcellulose medium and scored for CFU-Cs after 7 days (n = 7 per group, *P < .05 and **P < .01).

Analysis of the cell-intrinsic effects of Srf deletion. (A) Experimental outline of transplantation experiments. Srfflx/flx;Mx1-Cre whole BM cells (CD45.2, 4 × 106 totals) were transplanted into 6-week-old lethally irradiated wild-type littermate recipients (CD45.1). The recipients were treated or not with pIpC 4 weeks postengraftment to induce Srf-deletion exclusively in hematopoietic cells and not in BM stromal cells. Mice were analyzed 5 weeks after Cre induction. (B) Table of the hematologic parameters, BM cellularity, and spleen weight. Values shown are mean ± SEM (n = 7 per group, ***P < .001 by Mann-Whitney test). (C) Cell autonomous expansion of the LSK and MP compartments in recipient mice treated or not with pIpC. (n = 7 per group, *P < .05). (D) BM (2 × 104), spleen (2 × 105) and PB (5 × 105) cells of recipient mice treated or not with pIpC were plated in methylcellulose medium and scored for CFU-Cs after 7 days (n = 7 per group, *P < .05 and **P < .01).

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