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. 2021 May 24;11:10736. doi: 10.1038/s41598-021-90271-x

Figure 1.

Figure 1

Loss of CD13 leads to reduced bone volume and increased number of osteoclasts in 8–10 week old CD13-deficient mice. µCT reconstruction of cortical (a) and trabecular bone (b). (cf) Bone morphometry by µCT analysis; (c) BV/TV(%); Bone volume/Tissue volume, (d) Trabecular number, (e) Trabecular Thickness, (f) Trabecular Separation. (gi) Histomorphometric analysis of femurs of WT and CD13KO. Histology of femurs with (g), BV/TV(%), (h) Oc.S/BS; % OCs per bone surface (i), histochemical detection of TRAP+ osteoclasts (purple, indicated by the arrow). (j) Mineral apposition rate (MAR), (k) Bone formation rate (BFR/BS) measured by Osteomeasure software (OsteoMetrics, Decatur, USA) (https://www.osteometrics.com). All samples were scanned, reconstructed, and analyzed in a Scanco µCT40 running Evaluation Program V6.6 (http://www.scanco.ch/en/systems-solutions/software.html). Histochemical analysis of TRAP+ osteoclasts in bone sections were imaged with Zeiss fluorescence inverted microscope and analyzed by using Zeiss Zen 2.0 Pro blue edition software (https://www.zeiss.com/content/dam/Microscopy/Downloads/Pdf/FAQs/zen2-blue-edition_installation-guide.pdf). Scale bars-×5; 200 µm, ×10; 100 µm, ×20; 50 µm. Data represents ± SD. (N = 6; WT, N = 7; CD13KO. **p < 0.01).