Abstract
Osteocalcin, also called Bone Gla Protein (BGP), is the most abundant of the non-collagenous proteins of bone produced by osteoblasts. It consists of a single chain of 46-50 amino acids, according to the species, and contains three vitamin K-dependent gamma-carboxyglutamic acid residues (GLA), involved in its binding to calcium and hydroxylapatite. Accumulating evidences suggest its involvement in bone remodeling, its physiological role, however, is still unclear. In this study the adhesion properties and the biological effects of osteocalcin on osteoclasts have been analyzed using as an experimental model, human osteoclast-like cells derived from giant cell tumors of bone (GCT). Osteocalcin promoted adhesion and spreading of these cells, triggering the release of bone sialoprotein (BSP), osteopontin (OPN) and fibronectin (FN), that in turn induced the clustering in focal adhesions of beta 1 and beta 3 integrin chains. Spreading was dependent upon the synthesis of these proteins. In fact, when the cells were incubated in the presence of monensin during the adhesion assay, they still adhered but spreading did not occur, focal adhesions disappeared and BSP, OPN, and FN were accumulated in intracellular granules. Furthermore osteocalcin induced chemotaxis in a dose-dependent manner. The action of BGP on osteoclasts was mediated by an intracellular calcium increase due to release from thapsigargin-sensitive stores. These results provide evidences that BGP exerts a role in the resorption process, inducing intracellular signaling, migration and adhesion, followed by synthesis and secretion of endogenous proteins.
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- Arnett T. R., Dempster D. W. A comparative study of disaggregated chick and rat osteoclasts in vitro: effects of calcitonin and prostaglandins. Endocrinology. 1987 Feb;120(2):602–608. doi: 10.1210/endo-120-2-602. [DOI] [PubMed] [Google Scholar]
- Bianco P., Fisher L. W., Young M. F., Termine J. D., Robey P. G. Expression of bone sialoprotein (BSP) in developing human tissues. Calcif Tissue Int. 1991 Dec;49(6):421–426. doi: 10.1007/BF02555854. [DOI] [PubMed] [Google Scholar]
- Blair H. C., Kahn A. J., Crouch E. C., Jeffrey J. J., Teitelbaum S. L. Isolated osteoclasts resorb the organic and inorganic components of bone. J Cell Biol. 1986 Apr;102(4):1164–1172. doi: 10.1083/jcb.102.4.1164. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Borsi L., Carnemolla B., Castellani P., Rosellini C., Vecchio D., Allemanni G., Chang S. E., Taylor-Papadimitriou J., Pande H., Zardi L. Monoclonal antibodies in the analysis of fibronectin isoforms generated by alternative splicing of mRNA precursors in normal and transformed human cells. J Cell Biol. 1987 Mar;104(3):595–600. doi: 10.1083/jcb.104.3.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carnemolla B., Borsi L., Zardi L., Owens R. J., Baralle F. E. Localization of the cellular-fibronectin-specific epitope recognized by the monoclonal antibody IST-9 using fusion proteins expressed in E. coli. FEBS Lett. 1987 May 11;215(2):269–273. doi: 10.1016/0014-5793(87)80160-6. [DOI] [PubMed] [Google Scholar]
- Charo I. F., Nannizzi L., Smith J. W., Cheresh D. A. The vitronectin receptor alpha v beta 3 binds fibronectin and acts in concert with alpha 5 beta 1 in promoting cellular attachment and spreading on fibronectin. J Cell Biol. 1990 Dec;111(6 Pt 1):2795–2800. doi: 10.1083/jcb.111.6.2795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chenu C., Delmas P. D. Platelets contribute to circulating levels of bone sialoprotein in human. J Bone Miner Res. 1992 Jan;7(1):47–54. doi: 10.1002/jbmr.5650070108. [DOI] [PubMed] [Google Scholar]
- Conforti G., Zanetti A., Colella S., Abbadini M., Marchisio P. C., Pytela R., Giancotti F., Tarone G., Languino L. R., Dejana E. Interaction of fibronectin with cultured human endothelial cells: characterization of the specific receptor. Blood. 1989 May 1;73(6):1576–1585. [PubMed] [Google Scholar]
- Davies J., Warwick J., Totty N., Philp R., Helfrich M., Horton M. The osteoclast functional antigen, implicated in the regulation of bone resorption, is biochemically related to the vitronectin receptor. J Cell Biol. 1989 Oct;109(4 Pt 1):1817–1826. doi: 10.1083/jcb.109.4.1817. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DeFranco D. J., Glowacki J., Cox K. A., Lian J. B. Normal bone particles are preferentially resorbed in the presence of osteocalcin-deficient bone particles in vivo. Calcif Tissue Int. 1991 Jul;49(1):43–50. doi: 10.1007/BF02555901. [DOI] [PubMed] [Google Scholar]
- Dejana E., Colella S., Conforti G., Abbadini M., Gaboli M., Marchisio P. C. Fibronectin and vitronectin regulate the organization of their respective Arg-Gly-Asp adhesion receptors in cultured human endothelial cells. J Cell Biol. 1988 Sep;107(3):1215–1223. doi: 10.1083/jcb.107.3.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dejana E., Lampugnani M. G., Giorgi M., Gaboli M., Marchisio P. C. Fibrinogen induces endothelial cell adhesion and spreading via the release of endogenous matrix proteins and the recruitment of more than one integrin receptor. Blood. 1990 Apr 1;75(7):1509–1517. [PubMed] [Google Scholar]
- Desbois C., Hogue D. A., Karsenty G. The mouse osteocalcin gene cluster contains three genes with two separate spatial and temporal patterns of expression. J Biol Chem. 1994 Jan 14;269(2):1183–1190. [PubMed] [Google Scholar]
- Glowacki J., Lian J. B. Impaired recruitment and differentiation of osteoclast progenitors by osteocalcin-deplete bone implants. Cell Differ. 1987 Sep;21(4):247–254. doi: 10.1016/0045-6039(87)90479-9. [DOI] [PubMed] [Google Scholar]
- Glowacki J., Rey C., Glimcher M. J., Cox K. A., Lian J. A role for osteocalcin in osteoclast differentiation. J Cell Biochem. 1991 Mar;45(3):292–302. doi: 10.1002/jcb.240450312. [DOI] [PubMed] [Google Scholar]
- Grano M., Colucci S., De Bellis M., Zigrino P., Argentino L., Zambonin G., Serra M., Scotlandi K., Teti A., Zambonin Zallone A. New model for bone resorption study in vitro: human osteoclast-like cells from giant cell tumors of bone. J Bone Miner Res. 1994 Jul;9(7):1013–1020. doi: 10.1002/jbmr.5650090708. [DOI] [PubMed] [Google Scholar]
- Grano M., Zigrino P., Colucci S., Zambonin G., Trusolino L., Serra M., Baldini N., Teti A., Marchisio P. C., Zallone A. Z. Adhesion properties and integrin expression of cultured human osteoclast-like cells. Exp Cell Res. 1994 Jun;212(2):209–218. doi: 10.1006/excr.1994.1136. [DOI] [PubMed] [Google Scholar]
- Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
- Hauschka P. V., Lian J. B., Cole D. E., Gundberg C. M. Osteocalcin and matrix Gla protein: vitamin K-dependent proteins in bone. Physiol Rev. 1989 Jul;69(3):990–1047. doi: 10.1152/physrev.1989.69.3.990. [DOI] [PubMed] [Google Scholar]
- Helfrich M. H., Nesbitt S. A., Dorey E. L., Horton M. A. Rat osteoclasts adhere to a wide range of RGD (Arg-Gly-Asp) peptide-containing proteins, including the bone sialoproteins and fibronectin, via a beta 3 integrin. J Bone Miner Res. 1992 Mar;7(3):335–343. doi: 10.1002/jbmr.5650070314. [DOI] [PubMed] [Google Scholar]
- Holtrop M. E., King G. J. The ultrastructure of the osteoclast and its functional implications. Clin Orthop Relat Res. 1977 Mar-Apr;(123):177–196. [PubMed] [Google Scholar]
- Jaconi M. E., Theler J. M., Schlegel W., Appel R. D., Wright S. D., Lew P. D. Multiple elevations of cytosolic-free Ca2+ in human neutrophils: initiation by adherence receptors of the integrin family. J Cell Biol. 1991 Mar;112(6):1249–1257. doi: 10.1083/jcb.112.6.1249. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Juliano R. L., Haskill S. Signal transduction from the extracellular matrix. J Cell Biol. 1993 Feb;120(3):577–585. doi: 10.1083/jcb.120.3.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Loeser R. F., Wallin R. Cell adhesion to matrix Gla protein and its inhibition by an Arg-Gly-Asp-containing peptide. J Biol Chem. 1992 May 15;267(14):9459–9462. [PubMed] [Google Scholar]
- Malone J. D., Teitelbaum S. L., Griffin G. L., Senior R. M., Kahn A. J. Recruitment of osteoclast precursors by purified bone matrix constituents. J Cell Biol. 1982 Jan;92(1):227–230. doi: 10.1083/jcb.92.1.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Merle B., Delmas P. D. Normal carboxylation of circulating osteocalcin (bone Gla-protein) in Paget's disease of bone. Bone Miner. 1990 Nov;11(2):237–245. doi: 10.1016/0169-6009(90)90062-k. [DOI] [PubMed] [Google Scholar]
- Miyauchi A., Alvarez J., Greenfield E. M., Teti A., Grano M., Colucci S., Zambonin-Zallone A., Ross F. P., Teitelbaum S. L., Cheresh D. Recognition of osteopontin and related peptides by an alpha v beta 3 integrin stimulates immediate cell signals in osteoclasts. J Biol Chem. 1991 Oct 25;266(30):20369–20374. [PubMed] [Google Scholar]
- Mundy G. R., Poser J. W. Chemotactic activity of the gamma-carboxyglutamic acid containing protein in bone. Calcif Tissue Int. 1983;35(2):164–168. doi: 10.1007/BF02405025. [DOI] [PubMed] [Google Scholar]
- Mundy G. R., Varani J., Orr W., Gondek M. D., Ward P. A. Resorbing bone is chemotactic for monocytes. Nature. 1978 Sep 14;275(5676):132–135. doi: 10.1038/275132a0. [DOI] [PubMed] [Google Scholar]
- Paniccia R., Colucci S., Grano M., Serra M., Zallone A. Z., Teti A. Immediate cell signal by bone-related peptides in human osteoclast-like cells. Am J Physiol. 1993 Nov;265(5 Pt 1):C1289–C1297. doi: 10.1152/ajpcell.1993.265.5.C1289. [DOI] [PubMed] [Google Scholar]
- Pastoureau P., Vergnaud P., Meunier P. J., Delmas P. D. Osteopenia and bone-remodeling abnormalities in warfarin-treated lambs. J Bone Miner Res. 1993 Dec;8(12):1417–1426. doi: 10.1002/jbmr.5650081202. [DOI] [PubMed] [Google Scholar]
- Price P. A., Otsuka A. A., Poser J. W., Kristaponis J., Raman N. Characterization of a gamma-carboxyglutamic acid-containing protein from bone. Proc Natl Acad Sci U S A. 1976 May;73(5):1447–1451. doi: 10.1073/pnas.73.5.1447. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rahman S., Oberdorf A., Montecino M., Tanhauser S. M., Lian J. B., Stein G. S., Laipis P. J., Stein J. L. Multiple copies of the bone-specific osteocalcin gene in mouse and rat. Endocrinology. 1993 Dec;133(6):3050–3053. doi: 10.1210/endo.133.6.8243336. [DOI] [PubMed] [Google Scholar]
- Reinholt F. P., Hultenby K., Oldberg A., Heinegård D. Osteopontin--a possible anchor of osteoclasts to bone. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4473–4475. doi: 10.1073/pnas.87.12.4473. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ross F. P., Chappel J., Alvarez J. I., Sander D., Butler W. T., Farach-Carson M. C., Mintz K. A., Robey P. G., Teitelbaum S. L., Cheresh D. A. Interactions between the bone matrix proteins osteopontin and bone sialoprotein and the osteoclast integrin alpha v beta 3 potentiate bone resorption. J Biol Chem. 1993 May 5;268(13):9901–9907. [PubMed] [Google Scholar]
- Ruoslahti E. Integrins. J Clin Invest. 1991 Jan;87(1):1–5. doi: 10.1172/JCI114957. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takemura H., Hughes A. R., Thastrup O., Putney J. W., Jr Activation of calcium entry by the tumor promoter thapsigargin in parotid acinar cells. Evidence that an intracellular calcium pool and not an inositol phosphate regulates calcium fluxes at the plasma membrane. J Biol Chem. 1989 Jul 25;264(21):12266–12271. [PubMed] [Google Scholar]
- Tezuka K., Sato T., Kamioka H., Nijweide P. J., Tanaka K., Matsuo T., Ohta M., Kurihara N., Hakeda Y., Kumegawa M. Identification of osteopontin in isolated rabbit osteoclasts. Biochem Biophys Res Commun. 1992 Jul 31;186(2):911–917. doi: 10.1016/0006-291x(92)90832-6. [DOI] [PubMed] [Google Scholar]
- Vaes G. Cellular biology and biochemical mechanism of bone resorption. A review of recent developments on the formation, activation, and mode of action of osteoclasts. Clin Orthop Relat Res. 1988 Jun;(231):239–271. [PubMed] [Google Scholar]
- Zambonin-Zallone A., Teti A., Grano M., Rubinacci A., Abbadini M., Gaboli M., Marchisio P. C. Immunocytochemical distribution of extracellular matrix receptors in human osteoclasts: a beta 3 integrin is colocalized with vinculin and talin in the podosomes of osteoclastoma giant cells. Exp Cell Res. 1989 Jun;182(2):645–652. doi: 10.1016/0014-4827(89)90266-8. [DOI] [PubMed] [Google Scholar]