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3BP2-deficient mice are osteoporotic with impaired osteoblast and osteoclast functions
Noam Levaot, … , Ernst Reichenberger, Robert Rottapel
Noam Levaot, … , Ernst Reichenberger, Robert Rottapel
Published July 18, 2011
Citation Information: J Clin Invest. 2011;121(8):3244-3257. https://doi.org/10.1172/JCI45843.
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Research Article Bone biology

3BP2-deficient mice are osteoporotic with impaired osteoblast and osteoclast functions

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Abstract

A fine balance between bone resorption by osteoclasts and bone formation by osteoblasts maintains bone homeostasis. In patients with cherubism, gain-of-function mutations in 3BP2, which is encoded by SH3-domain binding protein 2 (SH3BP2), cause cystic lesions with activated osteoclasts that lead to craniofacial abnormalities. However, little is known about the function of wild-type 3BP2 in regulating bone homeostasis. Here we have shown that 3BP2 is required for the normal function of both osteoblasts and osteoclasts. Initial analysis showed that Sh3bp2–/–mice developed osteoporosis as a result of reduced bone formation despite the fact that bone resorption was impaired. We demonstrated using reciprocal bone marrow chimeras, a cell-intrinsic defect of the osteoblast and osteoclast compartments in vivo. Further, Sh3bp2–/– osteoblasts failed to mature and form mineralized nodules in vitro, while Sh3bp2–/– osteoclasts spread poorly and were unable to effectively degrade dentine matrix in vitro. Finally, we showed that 3BP2 was required for Abl activation in osteoblasts and Src activation in osteoclasts, and demonstrated that the in vitro defect of each cell type was restored by the respective expression of activated forms of these kinases. These findings reveal an unanticipated role for the 3BP2 adapter protein in osteoblast function and in coordinating bone homeostatic signals in both osteoclast and osteoblast lineages.

Authors

Noam Levaot, Paul D. Simoncic, Ioannis D. Dimitriou, Andrew Scotter, Jose La Rose, Adeline H.M. Ng, Thomas L. Willett, Chiachien J. Wang, Salima Janmohamed, Marc Grynpas, Ernst Reichenberger, Robert Rottapel

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Figure 2

Impaired bone resorption by Sh3bp2–/– osteoclasts.

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Impaired bone resorption by Sh3bp2–/– osteoclasts.
   
Histomorphometric...
Histomorphometric analysis of (A) OcS/BS, (B) N.Oc/BS, and (C) BV/TV in 12-week-old mice. n = 6; *P < 0.05. (D) Analysis of N.Nuclei/Oc in tibias of 12-week-old mice. Osteoclasts were sorted into groups with 1–2, 3–5, and 6+ N.Nuclei/Oc. n = 6. Quantitative PCR analysis of tnfsf11 (E) and tnfsf11b (F) transcript levels in the bones of 12-week-old wild-type and Sh3bp2–/– mice. n = 5. (G) ELISA measurement of basal serum CTX-I levels in 12-week-old wild-type and Sh3bp2–/– mice. n = 5; *P < 0.01. (H) TEM of vertebral sections from 4-week-old wild-type and Sh3bp2–/– mice showing representative osteoclasts exhibiting mature and attenuated ruffled borders from wild-type or Sh3bp2–/– mice, respectively. Scale bars: 2 μm. (I) Quantification of osteoclasts with mature ruffled borders. n = 50 osteoclasts from 3 wild-type and 3 Sh3bp2–/– mice (approximately 15 osteoclasts/mouse); P < 0.01. (J) Length measurements of 5-month-old wild-type or Sh3bp2–/– mice. The distance between the snout and anus is shown. n = 15 wild-type and 13 Sh3bp2–/– mice; P < 0.01. (K) μCT reconstruction of the femora of 16-week-old wild-type recipient mice, 8 weeks following the transfer of wild-type or Sh3bp2–/– bone marrow. Nonirradiated control is shown on the left. (L–N) μCT-derived measurements of (L) BV/TV, (M) Tb.Th, and (N) Tb.N. n = 8; *P < 0.05. (O and P) Histomorphometric analysis of (O) OcS/BS and (P) N.Oc/BS in the tibias of 16-week-old wild-type recipient mice, 8 weeks following the transfer of wild-type or Sh3bp2–/– bone marrow is shown. n = 4; *P < 0.05. Data are presented as mean ± SEM.

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