TY - JOUR
T1 - Gender-dependence of bone structure and properties in adult osteogenesis imperfecta murine model
AU - Yao, Xiaomei
AU - Carleton, Stephanie M.
AU - Kettle, Arin D.
AU - Melander, Jennifer
AU - Phillips, Charlotte L.
AU - Wang, Yong
N1 - Funding Information:
The authors gratefully thank Mark Dallas for assistance with µCT and three-point bending experiments. This work was supported by National Institutes of Health grant R01AR055907. This study utilized the Center for Research on Interfacial Structure and Properties (CRISP) and Center of Excellence in Mineralized Tissues (CEMT) facilities at the University of Missouri Kansas City.
PY - 2013/6
Y1 - 2013/6
N2 - Osteogenesis imperfecta (OI) is a dominant skeletal disorder characterized by bone fragility and deformities. Though the oim mouse model has been the most widely studied of the OI models, it has only recently been suggested to exhibit gender-dependent differences in bone mineralization. To characterize the impact of gender on the morphometry/ultra-structure, mechanical properties, and biochemical composition of oim bone on the congenic C57BL/J6 background, 4-month-old oim/oim, +/oim, and wild-type (wt) female and male tibiae were evaluated using micro-computed tomography, three-point bending, and Raman spectroscopy. Dramatic gender differences were evident in both cortical and trabecular bone morphological and geometric parameters. Male mice had inherently more bone and increased moment of inertia than genotype-matched female counterparts with corresponding increases in bone biomechanical strength. The primary influence of gender was structure/geometry in bone growth and mechanical properties, whereas the mineral/matrix composition and hydroxyproline content of bone were influenced primarily by the oim collagen mutation. This study provides evidence of the importance of gender in the evaluation and interpretation of potential therapeutic strategies when using mouse models of OI.
AB - Osteogenesis imperfecta (OI) is a dominant skeletal disorder characterized by bone fragility and deformities. Though the oim mouse model has been the most widely studied of the OI models, it has only recently been suggested to exhibit gender-dependent differences in bone mineralization. To characterize the impact of gender on the morphometry/ultra-structure, mechanical properties, and biochemical composition of oim bone on the congenic C57BL/J6 background, 4-month-old oim/oim, +/oim, and wild-type (wt) female and male tibiae were evaluated using micro-computed tomography, three-point bending, and Raman spectroscopy. Dramatic gender differences were evident in both cortical and trabecular bone morphological and geometric parameters. Male mice had inherently more bone and increased moment of inertia than genotype-matched female counterparts with corresponding increases in bone biomechanical strength. The primary influence of gender was structure/geometry in bone growth and mechanical properties, whereas the mineral/matrix composition and hydroxyproline content of bone were influenced primarily by the oim collagen mutation. This study provides evidence of the importance of gender in the evaluation and interpretation of potential therapeutic strategies when using mouse models of OI.
KW - Bone
KW - Gender
KW - Mouse
KW - Osteogenesis imperfecta
KW - oim/oim
UR - http://www.scopus.com/inward/record.url?scp=84886745523&partnerID=8YFLogxK
U2 - 10.1007/s10439-013-0793-7
DO - 10.1007/s10439-013-0793-7
M3 - Article
C2 - 23536112
AN - SCOPUS:84886745523
SN - 0090-6964
VL - 41
SP - 1139
EP - 1149
JO - Annals of biomedical engineering
JF - Annals of biomedical engineering
IS - 6
ER -