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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: Ann N Y Acad Sci. 2014 Aug 12;1335(1):100–109. doi: 10.1111/nyas.12502

Figure 1. FSH-R–mediated effects on bone formation and bone degradation.

Figure 1

(A). Whole vertebral cross section of the Fshr−/− mouse calcein labeled 5 and 1 d before sacrifice. In these 3 mm fields, the wild-type mouse (left) has typical short regions of labeling, while the knockout (right) shows a unique pattern with long regions of active bone formation. (B). Hematoxylin-stained cross sections at 20× (fields are 600 µm across) show typical variability in the wild-type (left), but uniform and smooth swiss cheese–like trabecular bone in the Fshr−/−. (C). A much greater proportion of bone was double labeled in the FSH-R−/− animal (p < 0.01). (D). Total calcein label was unchanged. (E). Linear cross-sectional length of calcein labeling was increased in the FSH-R−/− animal (p < 0.01), reflecting the size of bone forming units. (F). Trabecular thickness was increased in the Fshr−/− consistent with previous work,2 but had marginal statistical difference (p = 0.06) in this case.