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Annals of the Rheumatic Diseases logoLink to Annals of the Rheumatic Diseases
. 1993 Mar;52(3):182–184. doi: 10.1136/ard.52.3.182

Giant cells in arthritic synovium.

L S Wilkinson 1, A A Pitsillides 1, J C Edwards 1
PMCID: PMC1005014  PMID: 7683454

Abstract

OBJECTIVES: Giant cells are commonly present in inflamed synovium, often in close association with the intimal layer. The nature of these multinucleate cells has been reassessed using new cytochemical and immunochemical techniques. METHODS: Cryostat sections of non-inflamed, rheumatoid arthritic and osteoarthritic synovia were analysed for the presence of CD68 and non-specific esterase, markers associated with macrophages; activity of uridine diphosphoglucose dehydrogenase, associated with fibroblast-like synoviocytes; and tartrate resistant acid phosphatase and the vitronectin receptor subunit CD51, associated with osteoclasts. RESULTS: Giant cells were not seen in non-inflamed tissue. In diseased tissue giant cells in the intimal layer fell into two major groups: CD68 negative or dull cells with high uridine diphosphoglucose dehydrogenase (UDPGD) activity suggestive of true synoviocyte polykaryons; and CD68 positive cells with low UDPGD activity suggestive of macrophage polykaryons. The two groups were seen in samples from patients with rheumatoid arthritis (RA) and patients with osteoarthritis (OA), but the former were more prominent in OA and the latter in RA. Most CD68 positive giant cells also showed tartrate resistant acid phosphatase activity and prominent expression of CD51. As such they were histochemically indistinguishable from osteoclasts, but their bone resorbing capacity remains unknown. CONCLUSIONS: Giant cells in arthritic synovium appear to be of two types, one related to true synoviocytes and one to macrophages.

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Selected References

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  1. Athanasou N. A., Alvarez J. I., Ross F. P., Quinn J. M., Teitelbaum S. L. Species differences in the immunophenotype of osteoclasts and mononuclear phagocytes. Calcif Tissue Int. 1992 May;50(5):427–432. doi: 10.1007/BF00296773. [DOI] [PubMed] [Google Scholar]
  2. BARKA T. A simple azo-dye method for histochemical demonstration of acid phosphatase. Nature. 1960 Jul 16;187:248–249. doi: 10.1038/187248a0. [DOI] [PubMed] [Google Scholar]
  3. Chambers T. J. Multinucleate giant cells. J Pathol. 1978 Nov;126(3):125–148. doi: 10.1002/path.1711260302. [DOI] [PubMed] [Google Scholar]
  4. Enelow R. I., Sullivan G. W., Carper H. T., Mandell G. L. Induction of multinucleated giant cell formation from in vitro culture of human monocytes with interleukin-3 and interferon-gamma: comparison with other stimulating factors. Am J Respir Cell Mol Biol. 1992 Jan;6(1):57–62. doi: 10.1165/ajrcmb/6.1.57. [DOI] [PubMed] [Google Scholar]
  5. Franklin W. A., Mason D. Y., Pulford K., Falini B., Bliss E., Gatter K. C., Stein H., Clarke L. C., McGee J. O. Immunohistological analysis of human mononuclear phagocytes and dendritic cells by using monoclonal antibodies. Lab Invest. 1986 Mar;54(3):322–335. [PubMed] [Google Scholar]
  6. GOMORI G. Histochemistry of human esterases. J Histochem Cytochem. 1955 Nov;3(6):479–484. doi: 10.1177/3.6.479. [DOI] [PubMed] [Google Scholar]
  7. Grimley P. M., Sokoloff L. Synovial giant cells in rheumatoid arthritis. Am J Pathol. 1966 Nov;49(5):931–954. [PMC free article] [PubMed] [Google Scholar]
  8. Horton M. A., Lewis D., McNulty K., Pringle J. A., Chambers T. J. Monoclonal antibodies to osteoclastomas (giant cell bone tumors): definition of osteoclast-specific cellular antigens. Cancer Res. 1985 Nov;45(11 Pt 2):5663–5669. [PubMed] [Google Scholar]
  9. Marks S. C., Jr, Popoff S. N. Bone cell biology: the regulation of development, structure, and function in the skeleton. Am J Anat. 1988 Sep;183(1):1–44. doi: 10.1002/aja.1001830102. [DOI] [PubMed] [Google Scholar]
  10. Mehdizadeh S., Bitensky L., Chayen J. The assay of uridine diphosphoglucose dehydrogenase activity: discrimination from xanthine dehydrogenase activity. Cell Biochem Funct. 1991 Apr;9(2):103–110. doi: 10.1002/cbf.290090207. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. Wilkinson L. S., Pitsillides A. A., Worrall J. G., Edwards J. C. Light microscopic characterization of the fibroblast-like synovial intimal cell (synoviocyte). Arthritis Rheum. 1992 Oct;35(10):1179–1184. doi: 10.1002/art.1780351010. [DOI] [PubMed] [Google Scholar]
  13. Yam L. T., Li C. Y., Lam K. W. Tartrate-resistant acid phosphatase isoenzyme in the reticulum cells of leukemic reticuloendotheliosis. N Engl J Med. 1971 Feb 18;284(7):357–360. doi: 10.1056/NEJM197102182840704. [DOI] [PubMed] [Google Scholar]

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