Summary
Human osteoclasts, in contrast to mononuclear phagocytes, are known to express a well-defined restricted range of myeloid antigens. To determine whether these antigenic differences are present in other species, we examined the immunophenotype of chicken and rabbit ostoeclasts, macrophages, macrophage polykaryons, and monocytes and compared them with similarly derived and cultured human cells. Human, rabbit, and avian osteoclasts reacted with monoclonal antibodies against human β1 integrins (CD29, CD49b, CD49d), β3 integrins (CD51, CD61), as well as human macrophage-associated antigen CD68. Avian osteoclasts also reacted for CD11a/18 and CD14 which are not present on human osteoclasts. Avian and mammalian monocytes, macrophages, and macrophage polykaryons expressed all the above antigens. Both avian and human macrophage polykaryons produced by culture of peritoneal macrophages reacted with anti-CD51 antibodies indicating that expression of the vitronectin receptor alone does not distinguish between these cells in vitro.
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References
Vaes G (1988) Cellular biology and biochemical mechanism of bone resorption. Clin Orthop 231:239–271
Marks SC, Popoff SN (1988) Bone cell biology: the regulation of development, structure and function in the skeleton. Am J Anat 183:1–44
van Furth R (1980) Cells of the mononuclear phagocyte system-nomenclature in terms of sites and conditions. In: van Furth R (ed) Mononuclear phagocytes. Martinus Nijhoff, The Hague, pp 1–30
Athanasou NA, Wells CA, Quinn J, Ferguson DJP, Heryet A, McGee JO'D (1989) The origin and nature of stromal osteoclastlike multinucleated giant cells in breast cancer: implications for tumour osteolysis and macrophage biology. Br J Cancer 59:491–498
Udagawa N, Takahashi N, Akatsu T, Tanaka H, Sasaki T, Nishihara T, Koga T, Martin TJ, Suda T (1990) Origin of osteoclasts: mature monocytes and macrophages are capable of differentiating into osteoclasts under a suitable microenvironment prepared by bone marrow-derived stromal cells. Proc Natl Acad Sci USA 87:7260–7264
Athanasou NA, Quinn J (1990) Immunophenotypic differences between osteoclasts and macrophage polykaryons: immunohistological distinction and implications for osteoclast ontogeny and function. J Clin Pathol 43:997–1003
Horton MA, Chambers TJ (1986) Human osteoclast-specific antigens are expressed by osteoclasts in a wide range of nonhuman species. Br J Exp Pathol 67:95–104
Athanasou NA, Heryet A, Quinn J, Gatter KC, Mason DY, McGee JO'D (1986) Osteoclasts contain macrophage and megakaryocyte antigens. J Pathol 150:239–246
van Furth R, Cohn ZA (1968) The origin and kinetics of mononuclear phagocytes. J Exp Med 128:415–435
Minkin C (1982) Bone acid phosphatase: tartrate-resistant acid phosphatase as a marker of osteoclast function. Calcif Tissue Int 34:285–290
Chambers TJ, Magnus CJ (1982) Calcitonin alters behaviour of isolated osteoclasts. J Pathol 136:27–39
Hogg N, Horton MA (1987) Myeloid antigens: new and previously defined clusters. In: McMichael A (ed) Leucocyte typing III. Oxford University Press, Oxford.
Knapp W (1989) Leucocyte typing IV. Oxford University Press, Oxford
Gatter KC, Falini B, Mason DY (1984) The use of monoclonal antibodies in histopathological diagnosis. In: Anthony PP, Mac-Sween RNA (eds) Recent advances in histopathology, no. 12. Churchill Livingstone, Edinburgh, pp 35–67
Cheresh DA, Spiro RC (1987) Biosynthetic and functional properties of an Arg-Gly-Asp-directed receptor involved in human melanoma cell attachment to vitronectin, fibrinogen and von Willebrands factor. J Biol Chem 262:17703–17711
Oursler MJ, Bell LV, Clevinger B, Osdoby PJ (1985) Identification of osteoclast-specific monoclonal antibodies. J Cell Biol 100:1592–1600
Zambonin-Zallone A, Teti A, Primavera MV (1984) Monocytes from circulating blood fuse in vitro with purified osteoclasts in primary culture. J Cell Sci 66:335–342
Alvarez JI, Teiutelbaum SL, Blair HC, Grenfield DM, Athanasou NA, Ross FP (in press) Generation of avian osteoclast-like cells from mononuclear phagocytes. Endocrinology
Ferrero EM, Goyert SM (1989) Isolation and characterisation of a murine macrophage-specific gene. In: Knapp W, et al. (eds) Leucocyte typing IV. Oxford University Press, Oxford, pp 797–799
Kaplan G, Gaudernack G (1982) In vitro differentiation of human monocytes: differences in monocyte phenotypes induced by cultivation on glass or collagen. J Exp Med 156:1101–1114
Andreesen R, Brugger W, Scheiberbogen C, Kreutz M, Leser H-G, Rehm A, Lehr GW (1990) Surface phenotype analysis of human monocyte to macrophage maturation. J Leukocyte Biol 47:490–497
Uciechowski P, Schmidt RL (1989) Cluster Report: CD11. In: Knapp W, et al. (eds) Leucocyte typing IV. Oxford University Press, Oxford, pp 543–551
Horton MA, Rimmer EF, Lewis D, Pringle JAS, Fuller K, Chambers TJ (1984) Cell surface characterisation of the human osteoclast: phenotype relationship to other bone marrowderived cell types. J Pathol 144:281–294
Zambonin Zallone A, Teti A, Grano M, Rubinacci A, Abbadini M, Gaboli M, Marchisio PC (1989) Immunocytochemical distribution of extracellular matrix receptors in human osteoclasts: a beta 3 integrin is co-localised with vinculin and talin in the podosomes of osteoclastoma giant cells. Exp Cell Res 182:645–652
Horton MA, Davies J (1989) Adhesion receptors in bone. J Bone Miner Res 4:803–808
Athanasou NA, Quinn J, McGee JO'D (1989) Reactivity of Workshop MAb of the myeloid platelet and non-lineage (CD45, CD45R, CD11a,b,c) series with cells in bone and synovium. In: Knapp W (ed) Leucocyte typing IV. Oxford University Press, Oxford, pp 921–923
Springer TA (1990) Adhesion receptors of the immune system. Nature 346:425–434
Horton MA, Lewis D, McNulty K, Pringle JAS, Chambers TJ (1985) Monoclonal antibodies to osteoclastomas (giant cell bone tumours): definition of osteoclast-specific antigens. Cancer Res 45:5663–5669
Athanasou NA, Quinn J, Horton Ma, McGee JO'D (1990) New sites of cellular vitronectin receptor immunoreactivity detected with osteoclast-reacting monoclonal antibodies 13C2 and 23C6. Bone Miner 8:7–22
Hattersley G, Chambers TJ (1989) Generation of osteoclastic function in mouse bone marrow cultures: multinuclearity and tartrate-resistant acid phosphatase are unreliable markers for osteoclastic differentiation. Endocrinology 124:1689–1696
Kukita T, McManus LM, Miller M, Civin C, Roodman GD (1989) Osteoclast-like cells formed in long-term human bone marrow express a similar surface phenotype as authentic osteoclasts. Lab Invest 60:532–538
Takahashi N, Kukita T, MacDonald BC, Bird A, Mundy GR, McManus LM, Miller M, Boyde A, Jones SJ, Roodman GD (1989) Osteoclast-like cells form in long-term human bone marrow but not in peripheral blood cultures. J Clin Invest 83:543–550
Hayman EG, Pierschbucher MD, Ohgren Y, Ruoslahti E (1983) Serum spereading factor (vitronectin) is present at the cell surface. Proc Natl Acad Sci 80:4003–4007
Ferrero EM, Goyert SM (1989) Isolation and characterisation of a murine macrophage-specific gene. In: Knapp W (ed) Leucocyte typing IV, Oxford University Press, Oxford, pp 797–798
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Athanasou, N.A., Alvarez, J.I., Ross, F.P. et al. Species differences in the immunophenotype of osteoclasts and mononuclear phagocytes. Calcif Tissue Int 50, 427–432 (1992). https://doi.org/10.1007/BF00296773
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DOI: https://doi.org/10.1007/BF00296773