Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9104796 | Bone | 2005 | 7 Pages |
Abstract
LTBPs are extracellular matrix proteins resembling fibrillins. LTBP-1, 3, and 4 covalently bind latent TGF-β and modulate tissue levels of this potent cytokine through regulation of its secretion, localization, and/or activation. To address LTBP function in vivo, we generated Ltbp-3 null mice. Ltbp-3â/â animals developed craniofacial abnormalities due to early ossification of the skull base synchondroses and displayed reduced body size. In addition, histological examination of Ltbp-3â/â skeletons revealed an increase in bone mass. The osteoblast numbers and mineral apposition rates were decreased in Ltbp-3â/â mice, whereas the osteoclast numbers were similar in null and wild type mice. Histological examination revealed persistence of cartilage remnants in Ltbp-3â/â trabecular bone. Taken together, these results indicate that the Ltbp-3â/â high bone mass phenotype was due to a defect in bone resorption. We hypothesize that lack of Ltbp-3 results in decreased levels of TGF-β in bone and cartilage, which leads to compromised osteoclast function and decreased bone turnover.
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Authors
B. Dabovic, R. Levasseur, L. Zambuto, Y. Chen, G. Karsenty, D.B. Rifkin,