Skip to main content
Log in

Comparative studies of adherent rheumatoid synovial cells in primary culture: characterisation of the dendritic (Stellate) cell

  • Originals
  • Published:
Rheumatology International Aims and scope Submit manuscript

Summary

Primary cultures of adherent rheumatoid synovial cells contain variable proportions of fibroblasts, macrophages, and dendritic cells, as judged by morphological appearance. Comparative studies using various enzymic and histochemical staining procedures showed the dendritic cells to lack many of the characteristic features of macrophages, e.g. the failure to express HLA-DR (Ia) antigen. The dendritic cells and fibroblasts had several similarities, but differed to some extent in their nonspecific esterase activity, phagocytic and proliferative potential. As the proportions of dendritic cells and fibroblasts varied in relation to specific culture conditions, we examined the possibility that these morphologies might represent different functional states rather than distinct cellular origins. Using subcultured synovial fibroblasts with a uniform bipolar appearance, we have shown that exposure to interleukin-1 or mast cell products resulted in a transformation to dendritic morphology. This change in cell shape was prevented by the presence of indomethacin, but was subsequently achieved by the addition of exogenous PGE2. Thus it appears that the latter is the factor that modulates the morphological change of fibroblastic to dendritic cells. This study has also demonstrated the complete and reversible interchange of fibroblast/dendritic morphology, thereby confirming that these different shapes are manifest by the same cell. The changes in phenotypic expression associated with the dendritic appearance include increased production of collagenase, prostaglandin E, and nonspecific esterase, as well as an apparent inability to exhibit phagocytosis and to proliferate in culture. We conclude from our in vitro studies that the phenotypic behaviour of the synovial fibroblast (or synoviocyte) is very variable and dependent to a large extent upon local stimuli, but the identity and hierarchy of such stimulating and suppressive factors in relation to cellular interactions requires further study.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Dayer JM, Krane SM, Russell RGG, Robinson DR (1976) Production of collagenase and prostaglandins by isolated adherent synovial cells. Proc Natl Acad Sci USA 73:945–949

    Google Scholar 

  2. Woolley DE, Harris ED Jr, Mainardi CL, Brinckerhoff CE (1978) Collagenase immunolocalisation in cultures of rheumatoid synovial cells. Science 200:773–775

    Google Scholar 

  3. Woolley DE, Brinckerhoff CE, Mainardi CF, Vater CA, Evanson JM, Harris ED Jr (1979) Collagenase production by rheumatoid synovial cells: morphological and immunohistochemical studies of the dendritic cell. Ann Rheum Dis 38:262

    Google Scholar 

  4. Dayer JM, Goldring SR, Robinson DR, Krane SM (1980) Cell-cell interactions and collagenase production. In: Woolley DE, Evanson JM (eds) Collagenase in normal and pathological connective tissues. Wiley, New York, pp 83–104

    Google Scholar 

  5. Winchester RJ, Burmester GR (1981) Demonstration of Ia antigens on certain dendritic cells and on a novel elongate cell found in human synovial tissue. Scand J Immunol 14:439–444

    Google Scholar 

  6. Burmester GR, Dimitriu-Bona A, Waters SJ, Winchester RJ (1983) Identification of three major synovial lining cell populations by monoclonal antibodies directed to Ia antigens and antigens associated with monocytes/macrophages and fibroblasts. Scand J Immunol 17:69–82

    Google Scholar 

  7. Baker DG, Dayer JM, Roelke M, Schumacher HR, Krane SM (1983) Rheumatoid synovial cell morphologic changes induced by a mononuclear cell factor in culture. Arthritis Rheum 26:8–14

    Google Scholar 

  8. Bromley M, Woolley DE (1984) Histopathology of the rheumatoid lesion. Identification of cell types at sites of cartilage erosion. Arthritis Rheum 27:857–863

    Google Scholar 

  9. Woolley DE, Tetlow LC, Evanson JM (1980) Collagenase immunolocalisation studies of rheumatoid and malignant tissues. In: Woolley DE, Evanson JM (eds) Collagenase in normal and pathological connective tissues. Wiley, Chichester, pp 105–125

    Google Scholar 

  10. Steinman RM, Cohn ZA (1973) Identification of a novel cell type in peripheral lymphoid organs of mice. J Exp Med 139:380–397

    Google Scholar 

  11. Olah I, Rohlich P, Toro I (1968) A special type of cell in the medulla of the rat thymus. Acta Biol Acad Sci Hung 19:97–113

    Google Scholar 

  12. Veerman A (1974) On the interdigitating cells in the thymusdependent area of the rat spleen — a relation between the mononuclear phagocyte system and T-lymphocytes. Cell Tissue Res 148:247–257

    Google Scholar 

  13. Chen L, Adams J, Steinman RM (1978) Anatomy of germinal centers in mouse spleen with special reference to follicular dendritic cells. J Cell Biol 77:148–164

    Google Scholar 

  14. Thorbeck GJ, Silbergery-Sinakin I, Flotte TJ (1980) Langerhans cells as macrophages in skin and lymphoid organs. J Invest Dermatol 75:32–43

    Google Scholar 

  15. Van Voorhis WC, Hair LS, Steinman RM, Kaplan G (1982) Human dendritic cells. Enrichment and characterization from peripheral blood. J Exp Med 155:1172–1187

    Google Scholar 

  16. Van Voorhis WC, Witmer MD, Steinman RM (1983) The phenotype of dendritic cells and macrophages. Minisymposium presented by the American Association of Immunologists Federation proceedings, vol 42, no 14. Rockefeller University, New York, pp 3114–3118

    Google Scholar 

  17. Dayer JM, Russell RGG, Krane SM (1977) Collagenase production by rheumatoid synovial cells: stimulation by a human lymphocyte factor. Science 195:181–183

    Google Scholar 

  18. Dayer JM, Goldring SR, Robinson DR, Krane SM (1979) Effects of human mononuclear cell factor on cultured rheumatoid synovial cells. Interactions of prostaglandin E2 and cyclic adenosine 3',5'-monophosphate. Biochim Biophys Acta 586:87–105

    Google Scholar 

  19. Weissenfels M (1967) Method for acid phosphatase. In: Pearse AGE (ed) Histochemistry, 3rd edn. Little, Brown and Co, Boston, p 729

    Google Scholar 

  20. Gomori AL (1968) Method for alkaline phosphatase. In: Pearse AGE (ed) Histochemistry, 3rd edn. Little, Brown and Co, Boston, p 710

    Google Scholar 

  21. Yam LT, Li CY, Crosby WH (1971) Cytochemical identification of monocytes and granulocytes. Am J Clin Pathol 55:283–290

    Google Scholar 

  22. Li CY, Lam KW, Yam LT (1973) Method for α-napthyl-ASD chloracetate esterase. J Histochem Cytochem 21:1–12

    Google Scholar 

  23. Washstein D, Meisel J (1968) Lead method for adenosine triphosphate. In: Pearse AGE (ed) Histochemistry, 3rd edn. Little, Brown and Co, Boston, p 721

    Google Scholar 

  24. Graham RC, Karnovsky MJ (1966) Method for peroxidase staining. J Histochem Cytochem 14:291–302

    Google Scholar 

  25. Li CY, Lam KW, Yam LT (1973) Esterase in human leucocytes. Methods for aminocaproate esterase. J Histochem Cytochem 21:1–12

    Google Scholar 

  26. Lillie HG (1944) Oil red ‘O’ method for lipids. In: Pearse AGE (ed) Histochemistry, 3rd edn. Little, Brown and Co, Boston, p 697

    Google Scholar 

  27. Dingle JT, Fell HB (1975) Acridine orange method. ‘Lysosomes’, biology and pathology 2. North Holland/American Elsevier, New York, pp 609–612

    Google Scholar 

  28. Marshall AHE (1948) A method for the demonstration of reticuloendothelial cells in paraffin sections. J Pathol 60:515–517

    Google Scholar 

  29. Pearse AGE (1959) The periodic acid schiff's reaction. Carleton's histological technique, 4th edn. Drury and Wallington, Oxford, UK, pp 204–206

    Google Scholar 

  30. Oppenheimer-Marks N, Grinnell F (1981) Effects of plant lectins on the adhesive properties of baby hamster kidney cells. Eur J Cell Biol 23:286–294

    Google Scholar 

  31. Yoffe JR, Taylor DJ, Woolley DE (1984) Mast cell products stimulate collagenase and prostaglandin E production by cultures of adherent rheumatoid synovial cells. Biochem Biophys Res Commun 122:270–276

    Google Scholar 

  32. Hendler PL, Lavoic PE, Werb Z, Chan J, Seaman WE (1985) Human synovial dendritic cells. Direct observation of transition to fibroblasts. J Rheumatol 12:660–664

    Google Scholar 

  33. Amento EP, Bhan AK, McCullagh KG, Krane SM (1985) Influences of gamma interferon on synovial fibroblast like cells. Ia induction and inhibition of collagen synthesis. J Clin Invest 76:837–848

    Google Scholar 

  34. Dayer JM, Bread J, Chess L, Krane SM (1979) Participation of monocyte-macrophages and lymphocytes in the production of a factor that stimulates collagenase and prostaglandin release by rheumatoid synovial cells. J Clin Invest 64:1386–1392

    Google Scholar 

  35. Dayer JM, Russell RGG, Krane SM (1977) Collagenase production by rheumatoid synovial cells: stimulation by human lymphocyte factor. Science 195:181–183

    Google Scholar 

  36. Hammerman D, Stephens M, Barland P (1961) Comparative histology and metabolism of synovial tissue in normal and arthritic joints. In: Mills LC, Moyer JH (eds) Inflammation and diseases of connective tissue. Philadelphia, pp 158–168

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gadher, S.J., Woolley, D.E. Comparative studies of adherent rheumatoid synovial cells in primary culture: characterisation of the dendritic (Stellate) cell. Rheumatol Int 7, 13–22 (1987). https://doi.org/10.1007/BF00267337

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00267337

Key words

Navigation