Relationships of bone characteristics in MYO9B deficient femurs

• Published in: Journal of the mechanical behavior of biomedical materials Vol. 84; pp. 99 - 107
• Main Authors: Kim, Do-Gyoon, Jeong, Yong-Hoon, McMichael, Brooke K., Bähler, Martin, Bodnyk, Kyle, Sedlar, Ryan, Lee, Beth S.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ltd 01.08.2018
• Subjects: Animals; Biomechanical Phenomena; Biomechanics; Bone Density - genetics; Femur - metabolism; Femur - physiology; Gene Knockout Techniques; Knockout; Mechanical Phenomena; Mice; Multiscale characterization; MYO9B; Myosins - deficiency; Myosins - genetics; Biomechanics; MYO9B; Multiscale characterization; Knockout
• ISSN: 1751-6161; 1878-0180; 1878-0180
• DOI: 10.1016/j.jmbbm.2018.05.003

The objective of this study was to examine relationships among a variety of bone characteristics, including volumetric, mineral density, geometric, dynamic mechanical analysis, and static fracture mechanical properties. As MYO9B is an unconventional myosin in bone cells responsible for normal skeletal growth, bone characteristics of wild-type (WT), heterozygous (HET), and MYO9B knockout (KO) mice groups were compared as an animal model to express different bone quantity and quality. Forty-five sex-matched 12-week-old mice were used in this study. After euthanization, femurs were isolated and scanned using microcomputed tomography (micro-CT) to assess bone volumetric, tissue mineral density (TMD), and geometric parameters. Then, a non-destructive dynamic mechanical analysis (DMA) was performed by applying oscillatory bending displacement on the femur. Finally, the same femur was subject to static fracture testing. KO group had significantly lower length, bone mineral density (BMD), bone mass and volume, dynamic and static stiffness, and strength than WT and HET groups (p < 0.019). On the other hand, TMD parameters of KO group were comparable with those of WT group. HET group showed volumetric, geometric, and mechanical properties similar to WT group, but had lower TMD (p < 0.014). Non-destructive micro-CT and DMA parameters had significant positive correlations with strength (p < 0.015) without combined effect of groups and sex on the correlations (p > 0.077). This comprehensive characterization provides a better understanding of interactive behavior between the tissue- and organ-level of the same femur. The current findings elucidate that MYO9B is responsible for controlling bone volume to determine the growth rate and fracture risk of bone.