Osteoprotegerin Reduces the Serum Level of Receptor Activator of NF-κB Ligand Derived from Osteoblasts

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  • Yuko Nakamichi
    *Institute for Oral Science, Matsumoto Dental University, Nagano, Japan;
  • Nobuyuki Udagawa
    †Department of Biochemistry, Matsumoto Dental University, Nagano, Japan;
  • Yasuhiro Kobayashi
    *Institute for Oral Science, Matsumoto Dental University, Nagano, Japan;
  • Midrori Nakamura
    †Department of Biochemistry, Matsumoto Dental University, Nagano, Japan;
  • Yohei Yamamoto
    †Department of Biochemistry, Matsumoto Dental University, Nagano, Japan;
  • Teruhito Yamashita
    *Institute for Oral Science, Matsumoto Dental University, Nagano, Japan;
  • Toshihide Mizoguchi
    *Institute for Oral Science, Matsumoto Dental University, Nagano, Japan;
  • Masahiro Sato
    †Department of Biochemistry, Matsumoto Dental University, Nagano, Japan;
  • Makio Mogi
    ‡Department of Pharmacology, School of Dentistry, Aichi Gakuin University, Aichi, Japan; and
  • Josef M. Penninger
    §Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Vienna, Austria
  • Naoyuki Takahashi
    *Institute for Oral Science, Matsumoto Dental University, Nagano, Japan;

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<jats:title>Abstract</jats:title> <jats:p>Osteoprotegerin (OPG) is a decoy receptor for receptor activator of NF-κB ligand (RANKL). We previously reported that OPG deficiency elevated the circulating level of RANKL in mice. Using OPG−/− mice, we investigated whether OPG is involved in the shedding of RANKL by cells expressing RANKL. Osteoblasts and activated T cells in culture released a large amount of RANKL in the absence of OPG. OPG or a soluble form of receptor activator of NF-κB (the receptor of RANKL) suppressed the release of RANKL from those cells. OPG- and T cell-double-deficient mice showed an elevated serum RANKL level equivalent to that of OPG−/− mice, indicating that circulating RANKL is mainly derived from bone. The serum level of RANKL in OPG−/− mice was increased by ovariectomy or administration of 1α,25-dihydroxyvitamin D3. Expression of RANKL mRNA in bone, but not thymus or spleen, was increased in wild-type and OPG−/− mice by 1α,25-dihydroxyvitamin D3. These results suggest that OPG suppresses the shedding of RANKL from osteoblasts and that the serum RANKL in OPG−/− mice exactly reflects the state of bone resorption.</jats:p>

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