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Title: Characterization of two types of osteoclasts from human peripheral blood monocytes

Journal Article · · Biochemical and Biophysical Research Communications
 [1];  [2];  [3];  [2];  [2];  [4]
  1. Department of Microbiology, Mie University Graduate School of Medicine (Japan) and Department of Orthopaedic Surgery, Mie University Graduate School of Medicine (Japan)
  2. Department of Orthopaedic Surgery, Mie University Graduate School of Medicine (Japan)
  3. Department of Public Health, Yamagata University Graduate School of Medicine (Japan)
  4. Department of Microbiology, Mie University Graduate School of Medicine (Japan)

The two osteoclastogenesis pathways, receptor activator nuclear factor (NF)-{kappa}B ligand (RANKL)-mediated and fusion regulatory protein-1 (FRP-1)-mediated osteoclastogenesis, have recently been reported. There were significant differences in differentiation and activation mechanisms between the two pathways. When monocytes were cultured with FRP-1 without adding M-CSF, essential for the RANKL system, TRAP-positive polykaryocyte formation occurred. FRP-1-mediated osteoclasts formed larger pits on mineralized calcium phosphate plates than RANKL+M-CSF-mediated osteoclasts did. Lacunae on dentin surfaces induced by FRP-1-mediated osteoclasts were inclined to be single and isolated. However, osteoclasts induced by RANKL+M-CSF made many connected pits on dentin surfaces as if they crawled on there. Interestingly, FRP-1 osteoclastogenesis was enhanced by M-CSF/IL-1{alpha}, while chemotactic behavior to the dentin slices was not effected. There were differences in pH and concentration of HCO3- at culture endpoint and in adherent feature to dentin surfaces. Our findings indicate there are two types of osteoclasts with distinct properties.

OSTI ID:
20991321
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 356, Issue 2; Other Information: DOI: 10.1016/j.bbrc.2007.02.118; PII: S0006-291X(07)00384-1; Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

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