Areal Distribution of Preferential Alignment of Biological Apatite (BAp) Crystallite on Cross-Section of Center of Femoral Diaphysis in Osteopetrotic (op/op) Mouse

  • Lee Jee-Wook
    Divison of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University
  • Nakano Takayoshi
    Divison of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University
  • Toyosawa Satoru
    Department of Oral Pathology, Graduate School of Dentistry, Osaka University
  • Tabata Yasuhiko
    Institute for Frontier Medical Sciences, Kyoto University
  • Umakoshi Yukichi
    Divison of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University

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Osteoclasts are nearly non-existent in mutant osteopetrotic (op/op) mice due to defects in the expression of the macrophage colony-stimulating factor (M-CSF). Thus, areal distribution of the biological apatite (BAp) c-axis in a femoral cross-section of an op/op mouse was investigated using a microbeam X-ray diffraction system to understand the role of osteoclasts on formation of BAp preferential alignment.<BR>The incident X-ray beam is focused to 20 μm in diameter. The diffraction analysis is performed at 20 μm displacement intervals from the periosteal surface along the radial axis of the anterior portion at a cross-section of the femoral diaphysis. The osteopetrotic (op/op) mouse and its normal littermate used as a control were 12 weeks old.<BR>The lack of osteoclasts induces both abnormality of the skeletal system and calcification of the medullary cavity, which are typical features of osteopetrosis. Preferential alignment of the BAp c-axis in the osteopetrotic (op/op) mouse always shows a lower degree than that in the control mouse, regardless of the distance from the periosteum. Moreover, areal distributions of preferential alignment of the BAp c-axis on the femoral cross-section show quite different tendencies between the op/op and control mice. The preferential alignment of BAp gradually increases towards the periosteal surface in the op/op mouse due to the intramembranous ossification, while that in the control mouse is the lowest near the cortical envelope on the cross-section. This is because the decrease in the number of osteoclasts suppresses the normal modeling or remodeling, resulting in degradation of preferential alignment of the BAp c-axis as a bone quality parameter in the op/op mouse.

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