Modulation of the effects of osteoprotegerin (OPG) ligand in a human leukemic cell line by OPG and calcitonin

Citation
L. Mancini et al., Modulation of the effects of osteoprotegerin (OPG) ligand in a human leukemic cell line by OPG and calcitonin, BIOC BIOP R, 279(2), 2000, pp. 391-397
Citations number
30
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
279
Issue
2
Year of publication
2000
Pages
391 - 397
Database
ISI
SICI code
0006-291X(200012)279:2<391:MOTEOO>2.0.ZU;2-2
Abstract
The discovery of osteoprotegerin (OPG), osteoprotegerin ligand (OPGL), and RANK has elucidated the mechanism by which osteoblasts and stromal cells re gulate osteoclastic differentiation and function and mediate the effects ex erted by other hormones and cytokines. We have investigated the effects of these novel cytokines on the preosteoclastic cell line FLG 29.1. We show th at OPGL alone and in combination with macrophage colony-stimulating factor (CSF-1) dramatically reduced replication and increased tartrate-resistant a cid phosphatase activity. However, although FLG29.1 cells appear to adhere to the bone surface, they are not able to form resorption lacunae. OPG and calcitonin completely abolished the differentiation induced by OPGL. RANK w as detectable in FLG 29.1 and the number of positive cells was increased by OPGL/CSF-1 treatment while reduced by calcitonin. We propose that calciton in could interact with the OPG/OPGL, and its effects on RANK may explain in part the action of this hormone in suppressing bone resorption. (C) 2000 A cademic Press.