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3H-fucose incorporation into bone following exposure to parathyroid hormone, dibutyryl cyclic-AMP and colchicine

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Summary

Radioautographic and scintillation counting procedures were used to examine the effect of parathyroid hormone (PTH), dibutyryl cyclic-AMP (DB-cAMP), and colchicine on the incorporation of 3H-fucose into macromolecular material in organ cultures of bone. Radioautography demonstrated 3H-fucose incorporation into bone cells, with the heaviest uptake occurring in osteoclasts. A minimal incorporation occurred in pre-osteoblasts and osteoblasts of the osteogenic periosteum, and in fibroblasts of the fibrous periosteum. PTH appeared to produce a heavier label in association with osteoclasts while decreasing the limited labeling associated with cells of the osteogenic and fibrous periosteum. DB-cAMP and colchicine both markedly reduced the labeling associated with osteoclasts, while the minimal labeling of other bone cells remained. By contrast, scintillation counting results indicated that PTH had little or no effect on 3H-fucose incorporation, while DB-cAMP and colchicine considerably reduced the amount of labeled macromolecular material. The incorporation of 3H-fucose into glycoproteins and the role of glycoproteins are discussed.

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References

  • Bennett G (1978) Synthesis and migration of glycoproteins in cells of rat thymus, as shown by radioautography after 3H-fucose injection. Am J Anat 152:223–256

    Google Scholar 

  • Bennett G, Leblond CP (1977) Biosynthesis of the glycoproteins present in plasma membrane, lysosomes and secretory materials, as visualized by radioautography. Histochem J 9:393–417

    Google Scholar 

  • Bennett G, Leblond CP, Haddad A (1974) Migration of glycoprotein from the Golgi apparatus to the surface of various cell types as shown by radioautography after labeled fucose injection into rats. J Cell Biol 60:258–284

    Google Scholar 

  • Bingham PJ, Brazell IA, Owen M (1969) The effect of parathyroid extract on cellular activity and plasma calcium levels in vivo. J Endocrinol 45:387–400

    Google Scholar 

  • Bosmann HB, Hagopian A, Eylar EH (1969) Cellular membranes: The biosynthesis of glycoprotein and glycolipid in HeLa cell membranes. Arch Biochem Biophys 130:573–583

    Google Scholar 

  • Cameron DA (1972) The ultrastructure of bone. In: Bourne GH (ed) The biochemistry and physiology of bone. Academic Press, New York, ed 2, Vol 1, pp 191–236

    Google Scholar 

  • Della Corte E, Parkhouse RME (1973) Biosynthesis of immunoglobulin A (IgA). Secretion and addition of carbohydrate to monomer and polymer forms of mouse myeloma protein. Biochem J 136:589–596

    Google Scholar 

  • Dische Z (1963) Reciprocal relation between fucose and sialic acid in mammalian glycoproteins. Ann NY Acad Sci 106:259–260

    Google Scholar 

  • Doty SB, Schofield BH (1972) Electron microscopic localization of hydrolytic enzymes in osteoblasts. Histochem J 4:245–258

    Google Scholar 

  • Ehrlich HP, Ross R, Bornstein P (1974) Effect of anti-microtubular agents on the secretion of collagen. J Cell Biol 62:390–405

    Google Scholar 

  • Fleischer B (1978) The role of the Golgi apparatus in the synthesis of glycoproteins and glycolipids. In: Harmon RE (ed) Cell surface carbohydrate chemistry. Acad Press Inc, New York, pp 27–47

    Google Scholar 

  • Garland DL (1979) cAMP inhibits the in vitro assembly of microtubules. Arch Biochem Biophys 198:335–337

    Google Scholar 

  • Goldstone A, Koenig H (1970) Lysosomal hydrolases as glycoproteins. Life Sci 9:1341–1350

    Google Scholar 

  • Haddad A, Brasileiro ILG, Pelletier G (1979) Incorporation of L-(3H)-fucose into glycoproteins of the adrenal gland of mice. Light microscope radioautographic study on semi-thin sections. Cell Tissue Res 202:325–335

    Google Scholar 

  • Heersche JNM, Fedak SA, Aurbach GD (1971) The mode of action of dibutyryl adenosine 3′,5′monophosphate on bone tissue in vitro. J Biol Chem 246:6770–6775

    Google Scholar 

  • Holtrop ME, Raisz LG, Simmons HA (1974) The effects of parathyroid hormone, colchicine, and calcitonin on the ultrastructure and the activity of osteoclasts in organ culture. J Cell Biol 60:346–355

    Google Scholar 

  • Holtrop ME, King GJ (1977) The ultrastructure of the osteoclast and its functional implications. Clin Orthop 123:177–196

    Google Scholar 

  • Jansen HW, Bornstein P (1974) Effects of anti-microtubular agents on glycosaminoglycan synthesis and secretion by embryonic chick cartilage and chondrocytes. Biochim Biophys Acta 362:150–159

    Google Scholar 

  • Johnston CC Jr, Deiss WP, Miner EG (1962) Bone matrix biosynthesis in vitro. II. Effects of parathyroid hormone. J Biol Chem 237:3560–3565

    Google Scholar 

  • Johnston CCJr, Smith DM, Severson AR (1972) Bone resorption and matrix hexosamine labeling. In: Munson PL, Talmage RV (eds) Calcium, parathyroid hormone and the calcitonins. Excerpta Medica, Amsterdam, pp 327–337

    Google Scholar 

  • Luben RA, Cohen DV (1976) Effects of parathormone and calcitonin on citrate and hyaluronate metabolism in cultured bone. Endocrinology 98:413–419

    Google Scholar 

  • Luben RA, Goggins JF, Raisz LG (1974) Stimulation by parathyroid hormone of bone hyaluronate synthesis in organ culture. Endocrinology 94:737–745

    Google Scholar 

  • Moskalewski S, Thyberg J, Lohmander S, Friberg U (1975) Influence of colchicine and vinblastine on the Golgi complex and matrix deposition in chondrocyte aggregates. Exp Cell Res 95:440–454

    Google Scholar 

  • Munroe JR, Narasimhan S, Riordan J, Schachter H (1975) Intracellular localization of GDP-L-fucose: Glycoprotein and CMP-sialic acid: Apolipoprotein glycosyltransferases in rat and pork livers. Arch Biochem Biophys 169:269–277

    Google Scholar 

  • Owen M, Shetlar MR (1968) Uptake of 3H-glucosamine by osteoclasts. Nature 220:1335–1336

    Google Scholar 

  • Peck WA (1979) Cyclic AMP as a second messenger in the skeletal actions of parathyroid hormone: A decade-old hypothesis. Calcif Tissue Int 29:1–4

    Google Scholar 

  • Raisz LD, Holtrop ME, Simmons HA (1973) Inhibition of bone resorption by colchicine in organ culture. Endocrinology 92:556–562

    Google Scholar 

  • Schachter H, Jabbal I, Hudgin RL, Pinteric L, McGuire EJ, Roseman S (1970) Intracellular localization of liver sugar nucleotide glycoprotein glycosyltransferases in a Golgi-rich fraction. J Biol Chem 245:1090–1100

    Google Scholar 

  • Sear CHJ, Grant ME, Jackson DS (1977) Biosynthesis and release of glycoproteins by human skin fibroblasts in culture. Biochem J 168:91–103

    Google Scholar 

  • Severson AR, Rothberg PF, Pratt RM, Goggins JF (1973) Effects of parathyroid hormone on the incorporation of 3H-glucosamine into hyaluronic acid in bone organ culture. Endocrinology 92:1282–1285

    Google Scholar 

  • Shetlar MR, Shurley H, Hern D (1972) The effects of parathyroid extract upon incorporation of l-14C glucosamine into bone. Proc Soc Exp Biol Med 139:340–344

    Google Scholar 

  • Spiro RG (1969) Glycoproteins: Their biochemistry, biology and role in human disease. N Engl J Med 281:991–1001; 1043–1056

    Google Scholar 

  • Spiro RG (1973) Glycoproteins. Adv Protein Chem 27:349–467

    Google Scholar 

  • Vaes G (1968) Parathyroid hormone-like action of N6-2–0-dibutyryladenosine-3′,5′ (cyclic)monophosphate on bone explants in tissue culture. Nature 219:939–940

    Google Scholar 

  • Weinstock M (1979) Radioautographic visualization of 3H-fucose incorporation into glycoprotein by osteoblasts and its deposition into bone matrix. Calcif Tissue Int 27:177–185

    Google Scholar 

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This investigation was aided by grants from the Orthopaedic Research and Education Foundation and the Minnesota Medical Foundation. The author gratefully acknowledges the excellent technical assistance of Karen Brintzenhofe and Cynthia Park

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Severson, A.R. 3H-fucose incorporation into bone following exposure to parathyroid hormone, dibutyryl cyclic-AMP and colchicine. Cell Tissue Res. 214, 583–591 (1981). https://doi.org/10.1007/BF00233498

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