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

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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CD13 deficiency leads to marked reduction in trabecular bone volume and structure in 18–25 week old aged mice. (a–d) Bone morphometry by µCT analysis; (a), BV/TV(%); Bone volume/Tissue volume (b), Trabecular number, (c) Trabecular Thickness (d) Trabecular Separation. (e–h) Histomorphometric analysis (e), BV/TV(%), (f) Oc.S/BS; % OCs per bone surface, (g) Mineral apposition rate (MAR), (h) 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). Data represents ± SD. (N = 6; WT and N = 7; CD13^KO. ***p < 0.001, **p < 0.01, *p < 0.05).