<b>Chronological immunolocalization of sclerostin and FGF23 in the mouse metaphyseal trabecular and cortical </b><b>bone </b>

  • SAKURAI Atsunaka
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University Department of Restorative Dentistry, Graduate School of Dental Medicine, Hokkaido University
  • HASEGAWA Tomoka
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University
  • KUDO Ai
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University Department of Crown and Bridge Prosthodontics, Graduate School of Dental Medicine, Hokkaido University
  • SHEN Zhao
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University Department of Oral and Maxillofacial Surgery, Graduate School of Dental Medicine, Hokkaido University
  • NAGAI Tomoya
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University Department of Oral Functional Prosthodontics, Graduate School of Dental Medicine, Hokkaido University
  • ABE Miki
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University
  • YOSHIDA Taiji
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University
  • HONGO Hiromi
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University
  • YAMAMOTO Tomomaya
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University Self- Defense Force Hanshin Hospital
  • YAMAMOTO Tsuneyuki
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University
  • ODA Kimimitsu
    Biochemistry, Niigata University Graduate School of Medical and Dental Sciences
  • FREITAS Paulo Henrique Luiz de
    Department of Dentistry, Federal University of Sergipe at Lagarto
  • LI Minqi
    Shandong Provincial Key Laboratory of Oral Biomedicine, The School of Stomatology, Shandong University
  • SANO Hidehiko
    Department of Restorative Dentistry, Graduate School of Dental Medicine, Hokkaido University
  • AMIZUKA Norio
    Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University

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抄録

<p>To assess the chronological participation of sclerostin and FGF23 in bone metabolism, this study tracked the immunolocalization of sclerostin and FGF23 in the metaphyses of murine long bones from embryonic day 18 (E18) through 1 day after birth, 1 week, 2 weeks, 4 weeks, 8 weeks, and 20 weeks of age. We have selected two regions in the metaphyseal trabeculae for assessing sclerostin and FGF23 localization: close to the chondro-osseous junction, i.e., bone modeling site even in the adult animals, and the trabecular region distant from the growth plate, where bone remodeling takes place. As a consequence, sclerostin-immunopositive osteocytes could not be observed in both close and distant trabecular regions early at the embryonic and young adult stages. However, osteocytes gradually started to express sclerostin in the distant region earlier than in the close region of the trabeculae. Immunoreactivity for FGF23 was observed mainly in osteoblasts in the early stages, but detectable in osteocytes in the later stages of growth in trabecular and cortical bones. Fgf23 was weakly expressed in the embryonic and neonatal stages, while the receptors, Fgfr1c and αKlotho were strongly expressed in femora. At the adult stages, Fgf23 expression became more intense while Fgfr1c and aKlotho were weakly expressed. These findings suggest that sclerostin is secreted by osteocytes in mature bone undergoing remodeling while FGF23 is synthesized by osteoblasts and osteocytes depending on the developmental/growth stage. In addition, it appears that FGF23 acts in an autocrine and paracrine fashion in fetal and neonatal bones.</p>

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  • Biomedical Research

    Biomedical Research 38 (4), 257-267, 2017

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