Figure 7
Figure 7. Analysis of the effects (mean ± SEM) of iPTH treatment in WT and Wnt10b−/− mice. (A) Effects of iPTH on the relative frequency of BM LSK cells. (B-C) Effect of iPTH on the relative frequency of ST-HSPCs/MPP and LT-HSPCs. (D-F) Effect of iPTH on peripheral blood cell expansion after primary competitive repopulation. The percentages of CD11b+, GR-1+, and B220+ cells in the peripheral blood of untreated WT recipient mice are shown. Recipient mice received CD45.2+ BM donor cells from vehicle- and iPTH-treated WT and Wnt10−/− mice mixed in a 1:2 ratio with CD45.1+ competitor BM cells from untreated WT mice. (G-J) Kaplan-Meier survival analysis of WT mice transplanted with limiting number of BM cells derived from WT and Wnt10b−/− mice. (G-H) Donor mice were untreated. Recipient mice were treated with vehicle or iPTH for 4 weeks. (I-J) Donor mice were treated with vehicle or iPTH for 4 weeks. Recipient mice were untreated. n = 10 in each group. *P < .05 versus the corresponding vehicle-treated group.

Analysis of the effects (mean ± SEM) of iPTH treatment in WT and Wnt10b−/− mice. (A) Effects of iPTH on the relative frequency of BM LSK cells. (B-C) Effect of iPTH on the relative frequency of ST-HSPCs/MPP and LT-HSPCs. (D-F) Effect of iPTH on peripheral blood cell expansion after primary competitive repopulation. The percentages of CD11b+, GR-1+, and B220+ cells in the peripheral blood of untreated WT recipient mice are shown. Recipient mice received CD45.2+ BM donor cells from vehicle- and iPTH-treated WT and Wnt10−/− mice mixed in a 1:2 ratio with CD45.1+ competitor BM cells from untreated WT mice. (G-J) Kaplan-Meier survival analysis of WT mice transplanted with limiting number of BM cells derived from WT and Wnt10b−/− mice. (G-H) Donor mice were untreated. Recipient mice were treated with vehicle or iPTH for 4 weeks. (I-J) Donor mice were treated with vehicle or iPTH for 4 weeks. Recipient mice were untreated. n = 10 in each group. *P < .05 versus the corresponding vehicle-treated group.

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