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. 2017 Dec 5;1(26):2520–2528. doi: 10.1182/bloodadvances.2017011304

Figure 1.

Figure 1.

Phenotypic analysis of fresh and cultured OMs. (A) Representative data from the flow cytometric analysis of freshly isolated NCCs, NCCs cultured alone for 7 days (Cultured NCC), or cultured for 7 days with megakaryocytes (Cultured NCC+MK). In the example shown in the figure, cultures were initiated with 2 × 104 NCCs. On day 7, cultures contained 7 × 104 cells without and 1.8 × 105 cells with megakaryocytes, indicating that the number of CD45+F4/80+ cells in these cultures was ∼900 and 32 500 on day 7, respectively. Staining included CD41 to ensure that only CD41 cells were analyzed. (B) CD45+F/48+ OMs from NCCs or BM cells from long bones were cultured with RANKL and M-CSF to induce osteoclast formation. TRAP+ osteoclasts with ≥3 nuclei were quantified. *P < .05. (C) Osteoclasts formed from the calvariae-derived (left panel) OMs were replated on dentin, and resorption pits were stained after 3 days (right panel). Representative images of TRAP+ osteoclasts and resorption pits formed by these cells are shown. Slides were stained as described in “Materials and methods.” Scale bar indicates 50 μm.