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Inbred Strain‐Specific Response to Biglycan Deficiency in the Cortical Bone of C57BL6/129 and C3H/He Mice
Author(s) -
Wallace Joseph M,
Golcuk Kurtulus,
Morris Michael D,
Kohn David H
Publication year - 2009
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1359/jbmr.081259
Subject(s) - biglycan , inbred strain , strain (injury) , extracellular matrix , endocrinology , bone mineral , medicine , ratón , type i collagen , wild type , cortical bone , chemistry , biology , anatomy , mutant , gene , genetics , proteoglycan , osteoporosis , decorin
Inbred strain‐specific differences in mice exist in bone cross‐sectional geometry, mechanical properties, and indices of bone formation. Inbred strain‐specific responses to external stimuli also exist, but the role of background strain in response to genetic deletion is not fully understood. Biglycan (bgn) deficiency impacts bone through negative regulation of osteoblasts, resulting in extracellular matrix alterations and decreased mechanical properties. Because osteoblasts from C3H/He (C3H) mice are inherently more active versus osteoblasts from other inbred strains, and the bones of C3H mice are less responsive to other insults, it was hypothesized that C3H mice would be relatively more resistant to changes associated with bgn deficiency compared with C57BL6/129 (B6;129) mice. Changes in mRNA expression, tissue composition, mineral density, bone formation rate, cross‐sectional geometry, and mechanical properties were studied at 8 and 11 wk of age in the tibias of male wildtype and bgn‐deficient mice bred on B6;129 and C3H background strains. Bgn deficiency altered collagen cross‐linking and gene expression and the amount and composition of mineral in vivo. In bgn's absence, changes in collagen were independent of mouse strain. Bgn‐deficiency increased the amount of mineral in both strains, but changes in mineral composition, cross‐sectional geometry, and mechanical properties were dependent on genetic background. Bgn deficiency influenced the amount and composition of bone in mice from both strains at 8 wk, but C3H mice were better able to maintain properties close to wildtype (WT) levels. By 11 wk, most properties from C3H knockout (KO) bones were equal to or greater than WT levels, whereas phenotypic differences persisted in B6;129 KO mice. This is the first study into mouse strain‐specific changes in a small leucine‐rich proteoglycan gene disruption model in properties across the bone hierarchy and is also one of the first to relate these changes to mechanical competence. This study supports the importance of genetic factors in determining the response to a gene deletion and defines biglycan's importance to collagen and mineral composition in vivo.