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Transgenic mice overexpressing soluble osteoclast differentiation factor (sODF) exhibit severe osteoporosis.

Abstract
Osteoclast differentiation factor, ODF, also called RANKL, TRANCE, or OPGL, is a key molecule for osteoclast differentiation and activation, and is thought to act as a membrane-associated molecule in bone remodeling. Recent study suggested that soluble ODF (sODF) released from T cells also has some roles in bone resorption. To investigate the physiological and pathological function of sODF, we generated two types of transgenic mice overexpressing sODF. Mice overexpressing sODF ubiquitously from the early developmental stage died at the late fetal stage. The other type of mice, expressing sODF only in the liver after birth, grew to maturity with normal body size and weight. However, they exhibited a marked decrease in bone mineral density with aging compared with their non-transgenic littermates, and in addition, the strength of their femurs was extremely reduced. Histological analysis showed that the trabecular bone mass was decreased at 6 weeks of age and was sparse at age 3-4 months. The number of osteoclasts was significantly increased, while the number of osteoblasts was not altered on the surface of young trabecular bone. These results indicate that excessive production of sODF causes osteoporosis by accelerated osteoclastogenesis. The transgenic mouse overexpressing sODF in the liver could serve as a useful animal model for studying bone remodeling and evaluating therapeutic agents for osteoporosis.
AuthorsAtsuko Mizuno, Takeshi Kanno, Masaki Hoshi, Osamu Shibata, Kazuki Yano, Nobuaki Fujise, Masahiko Kinosaki, Kyoji Yamaguchi, Eisuke Tsuda, Akihiko Murakami, Hisataka Yasuda, Kanji Higashio
JournalJournal of bone and mineral metabolism (J Bone Miner Metab) Vol. 20 Issue 6 Pg. 337-44 ( 2002) ISSN: 0914-8779 [Print] Japan
PMID12434161 (Publication Type: Journal Article)
Chemical References
  • Carrier Proteins
  • Membrane Glycoproteins
  • RANK Ligand
  • Receptor Activator of Nuclear Factor-kappa B
  • Tnfrsf11a protein, mouse
  • Tnfsf11 protein, mouse
Topics
  • Acute Disease
  • Animals
  • Body Weight
  • Bone Density
  • Carrier Proteins (genetics, metabolism)
  • Disease Models, Animal
  • Fetal Death
  • Liver (metabolism)
  • Membrane Glycoproteins (genetics, metabolism)
  • Mice
  • Mice, Transgenic
  • Osteoclasts (metabolism)
  • Osteoporosis (genetics, metabolism, pathology, physiopathology)
  • RANK Ligand
  • Receptor Activator of Nuclear Factor-kappa B
  • Solubility

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