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. Author manuscript; available in PMC: 2019 Jul 1.
Published in final edited form as: J Bone Miner Res. 2018 Apr 25;33(7):1362–1375. doi: 10.1002/jbmr.3422

Figure 6. Osteoclast activity is increased in Hdac4ob−/− mice.

Figure 6.

(A) TRAP staining of tibiae of female 10-week-old Hdac4fl/fl and Hdac4ob−/− mice treated with PTH or vehicle is shown. 20X. (B) Quantification of osteoclast number and (C) osteoclast surface % in the animals in (A). Data shown as means ± SE. Different letters indicate p<0.05 vs. one another. (Hdac4 fl/fl; n=4, Hdac4 fl/fl with PTH; n=5, Hdac4ob−/−; n=−5, Hdac4ob−/−; with PTH; n=4). (D) Serum CTX levels (Hdac4 fl/fl; n=9, Hdac4 fl/fl with PTH; n=10, Hdac4ob−/−; n=10, Hdac4ob−/− with PTH; n=10), data shown as means ± SE and different letters indicate p<0.05 vs. one another. (E) The relative levels of Mmp13 mRNA normalized to β-actin (Hdac4 fl/fl; n=7, Hdac4 fl/fl with PTH; n=7, Hdac4ob−/−; n=6, Hdac4ob−/− with PTH; n=8). Total RNA was extracted from distal femurs of 10-week-old females and measured using real time RT-PCR. Data are shown as fold change to vehicle-treated Hdac4fl/fl and as means ± SE. Different letters indicate p<0.05 vs. one another.