Figure 3.
Lepr-cre+cells divide BM MSCs into 2 functionally distinct subpopulations. (A) Lepr-cre+;iDTRki/wt mice were injected with DT for 3 consecutive days and the effect on niche cells was analyzed on day 4. Control (Ctrl), n = 10; Cre+ iDTR+, n = 10; pool of 3 experiments. (B) In vitro differentiation of sorter-purified indicated cells using adipogenic or osteogenic culture conditions. Scale bars, 100 μm. Lepr+/−, n = 2; OP, n = 4; Endo, n = 5. ns, not significant.

Lepr-cre+cells divide BM MSCs into 2 functionally distinct subpopulations. (A) Lepr-cre+;iDTRki/wt mice were injected with DT for 3 consecutive days and the effect on niche cells was analyzed on day 4. Control (Ctrl), n = 10; Cre+ iDTR+, n = 10; pool of 3 experiments. (B) In vitro differentiation of sorter-purified indicated cells using adipogenic or osteogenic culture conditions. Scale bars, 100 μm. Lepr+/−, n = 2; OP, n = 4; Endo, n = 5. ns, not significant.

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