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Ultrastructural localization and biochemical characterization of vitronectin in developing rat bone

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This study has used light and electron microscope immunohistochemical and biochemical methods to localize and characterize vitronectin in early bone formation of developing rat mandible with rabbit antimurine vitronectin IgG. Developing jaws of foetuses were collected at embryonic day 15 (day 15) to day 18 from pregnant Wistar rats. After aldehyde fixation, specimens with and without osmium post-fixation were dehydrated and embedded in paraffin, Spurr's resin or LR gold resin for morphological and immunohistochemical examinations. At the light microscope level, in day 15 samples, positive vitronectin immunostaining was observed in small elongated areas of intercellular matrix and osteoblasts. Concomitant with initiation of matrix mineralization at day 16, vitronectin staining was similarly observed in small elongated areas containing intercellular matrix and osteoblasts but not clearly detected in fully mineralized bone matrix. The same staining profile was observed at days 17 and 18. At the ultrastructural level, immunogold particles were clearly detected over unmineralized matrix and cisterns of the rough-surfaced endoplasmic reticulum and the Golgi apparatus of osteoblasts as well as over demineralized bone matrix at day 16--18. In order to assess the presence of vitronectin in the mineral phase, mineral-binding bone proteins were extracted from fresh day 18 specimens using a three-step technique: 4 m guanidine HCl (G1 extract), aqueous EDTA without guanidine HCl (E extract), followed by guanidine HCl. Subsequent Western blot analysis of sodium dodecyl sulphate (SDS)--polyacrylamide gel electrophoresis revealed that the antibodies produced only a single band at an Mr of approximately 73 000 in both G1 and E extracts, indicating the presence of vitronectin in the mineralized bone matrix. These results indicate that, at the onset of bone formation, osteoblasts synthesize and release vitronectin, which is subsequently incorporated into the bone matrix and becomes a specific component of bone tissues. The observation of vitronectin in these critical stages of bone formation suggests that it may be involved in the regulation of bone formation. © 1998 Chapman & Hall

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References

  • Bernald, G.W. & Pease, D.C. (1969) An electron microscopic study of initial intramembranous osteogenesis. Am. J. Anat. 125, 271–90.

    Google Scholar 

  • Champbell, K.P., Maclennan, D.H. & Jorgensen, A.O. (1983) Staining of the Ca2+-binding proteins, calsequestrin, calmodulin, troponin C, and S-100, with the cationic carbocyanine dye 'stains-all'. J. Biol. Chem. 258, 11267–73.

    Google Scholar 

  • Dano, K., Andreasen, P.A., Grondahl-Hansen, J., Kristensen, P., Nielsen, L.S. & Skriver, L. (1985) Plasminogen activators, tissue degradation, and cancer. Adv. Cancer Res. 44, 139–266.

    Google Scholar 

  • Declerck, P. J., De-Mol, M., Alessi, M.C., Baudner, S., PÂques, E.P., Preissner, K.T., MÜller-Berghaus, G. & Collen, D. (1988) Purification and characterization of a plasminogen activator inhibitor 1 binding protein from human plasma. Identification as a multimeric form of S protein (vitronectin). J. Biol. Chem. 263, 15454–61.

    Google Scholar 

  • Domenicucci, C., Goldberg, H.A., Hofmann, T., Isenman, D., Wasi, S. & Sodek, J. (1988) Characterization of porcine osteonectin extracted from foetal calvariae. Biochem. J. 253, 139–51.

    Google Scholar 

  • Fairbanks, G., Steck, T.L. & Wallach, D.F.H. (1971) Electrophoretic analysis of major polypeptides of the human erythrocyte membrane. Biochemistry 10, 2606–17.

    Google Scholar 

  • Goldberg, H.A., Domenicucci, C. Pringle, G.A. & Sodek, J. (1988) Mineral-binding proteoglycans of fetal porcine calvarial bone. J. Biol. Chem. 263, 12092–101.

    Google Scholar 

  • Graham, R.C. Jr., & Karnovsky, M. J. (1966) The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J. Histochem. Cytochem. 14, 291–302.

    Google Scholar 

  • Grzesik, W. J. & Robey, P.G. (1994) Bone matrix RGD glycoproteins: immunolocalization and interaction with human primary osteoblastic bone cells in vitro. J. Bone. Miner. Res. 9, 487–96.

    Google Scholar 

  • HÄckel, C., Radig, K., RÖse, I. & Roessner, A. (1995) The urokinase plasminogen activator (u-PA) and its inhibitor (PAI-1) in embryo-fetal bone formation in the human: an immunohistochemical study. Anat. Embryol. 192, 363–8.

    Google Scholar 

  • Karnovsky, M. J. (1961) A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron microscopy. J. Cell. Biol. 27, 137A.

    Google Scholar 

  • Kupchella, C.E., Matsuoka, L.Y., Bryan, B., Wortsmann, J. & Dietrich, J.G. (1984) Histochemical evaluation of glycosaminoglycan deposition in the skin. J. Histochem. Cytochem. 32, 1121–24.

    Google Scholar 

  • Laemmli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–5.

    Google Scholar 

  • Lakkakorpi, P.T., Horton, M.A., Helfrich, M.H., Karhukorpi, E.-K. & VÄÄnÄnen, H.K. (1991) Vitronectin receptor has a role in bone resorption but does not mediate tight sealing zone attachment of osteoclasts to the bone surface. J. Cell. Biol. 115, 1179–86.

    Google Scholar 

  • Li, C.Y., Ziesmer, S.C. & Lazcano-Villareal, O. (1987) Use of azide and hydrogen peroxide as an inhibitor for endogenous peroxidase in the immunoperoxidase method. J. Histochem. Cytochem. 35, 1457–60.

    Google Scholar 

  • Martin, T. J., Allan, E.H. & Fukumoto, S. (1993) The plasminogen activator and inhibitor system in bone remodelling. Growth Regul. 3, 209–14.

    Google Scholar 

  • Merril, C.R., Goldman, D. & Van keuren, M.L. (1982) Simplified silver protein detection and image enhancement methods in polyacrylamide gels. Electrophoresis 3, 17–23.

    Google Scholar 

  • Mimuro, J. & Loskutoff, D. J. (1989) Purification of a protein from bovine plasma that binds to type 1 plasminogen activator inhibitor and prevents its interaction with extracellular matrix. Evidence that the protein is vitronectin. J. Biol. Chem. 264, 936–9.

    Google Scholar 

  • Otter, M., Kuiper, J., Ri jken, D. & Van zonneveld, A. J. (1995) Hepatocellular localisation of biosynthesis of vitronectin. Characterisation of the primary structure of rat vitronectin. Biochem. Mol. Biol. Int. 37, 563–72.

    Google Scholar 

  • Preissner, K.T. (1991) Structure and biological role of vitronectin. Annu. Rev. Cell. Biol. 7, 275–310.

    Google Scholar 

  • Saksela, O. & Rifkin, D.B. (1988) Cell-associated plasminogen activation: regulation and physiological functions. Annu. Rev. Cell Biol. 4, 93–126.

    Google Scholar 

  • Sato, T. (1968) A modified method for lead staining of the sections. J. Electron Microsc. 17, 158–9.

    Google Scholar 

  • Seiffert, D. (1996) Detection of vitronectin in mineralized bone matrix. J. Histochem. Cytochem. 44, 275–80.

    Google Scholar 

  • Seiffert, D., Wagner, N.N. & Loskutoff, D. J. (1990) Serum-derived vitronectin influences the pericellular distribution of type 1 plasminogen activator inhibitor. J. Cell. Biol. 111, 1283–91.

    Google Scholar 

  • Seiffert, D., Keeton, M., Eguchi, Y., Sawdey, M. & Loskutoff, D. J. (1991) Detection of vitronectin mRNA in tissues and cells of the mouse. Proc. Natl. Acad. Sci. USA 88, 9402–6.

    Google Scholar 

  • Seiffert, D., Crain, K., Wagner, N.V. & Loskutoff, D. J. (1994) Vitronectin gene expression in vivo. Evidence for extrahepatic synthesis and acute phase regulation. J. Biol. Chem. 269, 19836–42.

    Google Scholar 

  • Spurr, A.R. (1969) A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26, 31–43.

    Google Scholar 

  • Termine, J.D., Belcourt, A.B., Christner, P. J., Conn, K.M. & Nylen, M.U. (1980) Properties of dissociatively extracted fetal tooth matrix proteins. I. Principal molecular species in developing bovine enamel. J. Biol. Chem. 255, 9760–8.

    Google Scholar 

  • Termine, J.D., Belcourt, A.B., Conn, K.M. & Kleinman, H.K. (1981) Mineral and collagen-binding proteins of fetal calf bone. J. Biol. Chem. 256, 10403–8.

    Google Scholar 

  • Tokuyasu, K.T. (1986) Application of cryoultramicrotomy to immunocytochemistry. J. Microsc. 143, 139–49.

    Google Scholar 

  • Tomasini, B.R. & Mosher, D.F. (1990) Vitronectin. In Progress in Hemostasis and Thrombosis (edited by Coller, B.), pp. 269–75. Philadelphia: W.B. Saunders.

    Google Scholar 

  • Vila-Porcile, E., Picart, R., Tixier-Vidal, A. & Tougard, C. (1987) Cellular and subcellular distribution of laminin in adult rat anterior pituitary. J. Histochem. Cytochem. 35, 287–99.

    Google Scholar 

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Kumagai, T., Lee, I., Ono, Y. et al. Ultrastructural localization and biochemical characterization of vitronectin in developing rat bone. Histochem J 30, 111–119 (1998). https://doi.org/10.1023/A:1003235100960

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