Genetic regulation of cortical and trabecular bone strength and microstructure in inbred strains of mice

Charles H. Turner, Yeou Fang Hsieh, Ralph Müller, Mary L. Bouxsein, David J. Baylink, Clifford J. Rosen, Marc D. Grynpas, Leah Rae Donahue, Wesley G. Beamer

Research output: Contribution to journalArticlepeer-review

Abstract

The inbred strains of mice C57BL/6J (B6) and C3H/HeJ (C3H) have very different femoral peak bone densities and may serve as models for studying the genetic regulation of bone mass. Our objective was to further define the bone biomechanics and microstructure of these two inbred strains. Microarchitecture of the proximal femur, femoral midshaft, and lumbar vertebrae were evaluated in three dimensions using micro-computed tomography (υCT) with an isotropic voxel size of 17 υm. Mineralization of the distal femur was determined using quantitative back-scatter electron (BSE) imaging. υCT images suggested that C3H mice had thicker femoral and vertebral cortices compared with B6. The C3H bone tissue also was more highly mineralized. However, C3H mice had few trabeculate in the vertebral bodies, femoral neck, and greater trochanter. The trabecular number (Tb.N) in the C3H vertebral bodies was about half of that in B6 vertebrae (2.8-1 ± 0.1 mm- 1 vs 5.1-1 ± 0.2 mm-1; p < 0.0001). The thick, more highly mineralized femoral cortex of C3H mice resulted in greater bending strength of the femoral diaphysis (62.1 ± 1.2N vs. 27.4 ± 0.5N, p < 0.0001). In contrast, strengths of the lumbar vertebra were not significantly different between inbred strains (p = 0.5), presumably because the thicker cortices were combined with inferior trabecular structure in the vertebrae of C3H mice. These results indicate that C3H mice benefit from alleles that enhance femoral strength but paradoxically are deficient in trabecular bone structure in the lumbar vertebrae.

Original languageEnglish
Pages (from-to)1126-1131
Number of pages6
JournalJournal of Bone and Mineral Research
Volume15
Issue number6
DOIs
StatePublished - 2000

ASJC Scopus Subject Areas

  • Endocrinology, Diabetes and Metabolism
  • Orthopedics and Sports Medicine

Keywords

  • Biomechanics
  • Bone density
  • Genetics
  • Osteoporosis

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