Skip to main content
Log in

Ultrastructural features of the lymphocyte-stimulated halos produced by human glioma-derived cells in vitro

  • Published:
Journal of Neuro-Oncology Aims and scope Submit manuscript

Summary

Many glioma-derived cell lines have the capability of escaping cell-mediated immune attack. One mechanism of escape is the secretion of a hyaluronidase-sensitive mucopolysaccharide coat by these cells. This coat prevents contact and tumor cell killing by specific cytolytic allogeneic lymphocytes. The production of the coat by the tumor cells is stimulated by a macromolecular factor released by peripheral blood mononuclear (PBMC) cells in culture. We have examined the morphologic and ultrastructural features of this extracellular matrix. Three coat-producing lines were studied. Under phase contrast light microscopy, the coat is a clear pericellular ‘halo’. To stain this zone, ruthenium red and Alcian Blue 8 G stains, which bind to acid mucopolysaccharides (to a large extent, hyaluronic acid), were used. The two stains produced similar results. With light microscopy, a weblike pattern of stain was evident throughout the halo region. With transmission electron microscopy, staining was found along the plasma membrane of the glioma cells and their microvilli, stretching in long, branching filaments from these surfaces and, in some instances, from one microvillus to the next. Since mucopolysaccharide matrices have a large aqueous component, it was necessary to determine whether dehydration alters the stain pattern. Therefore, undehydrated ruthenium red stained specimens from each culture were embedded in Quetal 651 (Ted Pella, Inc., Tustin, CA), a water soluble plastic. No morphologic differences were noted between the hydrated and dehydrated specimens. This study indicates that numerous long microvilli and a secreted mucopolysaccharide matrix are important structural elements of the lymphocyte-stimulated tumor cell halo in vitro.

The mechanism by which the PBMC factor stimulates coat formation and the importance of the coat in in vivo tumor defenses remain to be elucidated.

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.

Similar content being viewed by others

References

  1. Dick SJ, Macchi B, Papazoglou S, Oldfield EH, Kornblith PL, Smith BH, Gately MK: Lymphoid cell-glioma cell interaction enhances cell coat production by human gliomas: Novel suppressor mechanism. Science 220:739–742, 1983.

    Google Scholar 

  2. Gately MK, Dick SJ, Dick MD, Macchi B, Oldfield EH, Papazoglou S, Kornblith PL: Independent requirements for helper factor and enzymatic removal of cell coats in the generation of lymphocytes cytotoxic for allogeneic human glioma cells. (Abs 260) Fed Proc 41:312, 1982.

    Google Scholar 

  3. Gately MK, Glaser M, Dick SJ, Mettetal RW Jr, Kornblith PL: In vitro studies on the cell-mediated immune response to human brain tumors. I. Requirement for third-party stimulator lymphocytes in the induction of cell-mediated cytotoxic responses to allogeneic cultured gliomas. JNCI 69:1245–1254, 1982.

    Google Scholar 

  4. Gately MK, Glaser M, McCarron RM, Dick SJ, Dick MD, Mettetal RW Jr, Kornblith PL: Mechanisms by which human gliomas may escape cellular immune attack. Acta Neurochir 64:175–197, 1982.

    Google Scholar 

  5. Gately CL, Muul LM, Greenwood MA, Papazoglou S, Dick SJ, Kornblith PL, Smith BH, Gately MK: In vitro studies on the cell-mediated immune response to human brain tumors. II. Leukocyte-induced coats of glycosaminoglycan increase the resistance of glioma cells to cellular immune attack. J Immunol 133:3387–3395, 1984.

    Google Scholar 

  6. Clarris BJ, Fraser JRE: On the pericellular zone of some mammalian cell in vitro. Expt Cell Res 49:181–193, 1968.

    Google Scholar 

  7. McBride WH, Bard JB: Hyaluronidase-sensitive halos around adherent cells. Their role in blocking lymphocyte-mediated cytolysis. J Exp Med 149:507–515, 1979.

    Google Scholar 

  8. Mikuni-Takagaki Y, Toole BP: Shedding of hyaluronate from the cell surface of Rous sarcoma virus transformed chondrocytes. J Biol Chem 254:8409–8415, 1979.

    Google Scholar 

  9. Hopwood JJ, Dorfman A: Glycosaminoglycans synthesis by cultured human skin fibroblasts after transformation with simian virus 40. J Biol Chem 252:4777–4785, 1977.

    Google Scholar 

  10. Makita A, Shimojo H: Polysaccharides of SV40-transformed green monkey kidney cells. Biochim Biophys Acta 304:571–574, 1973.

    Google Scholar 

  11. Satch C, Duff R, Rapp R, Davidson EA: Production of mucopolysaccharides by normal transformed cells. Proc Natl Acad Sci USA 70:54–56, 1973.

    Google Scholar 

  12. Bader JP: Temperature-dependent transformation of cells infected with a mutant of Bryan Rous sarcoma virus. J Virol 10:267–270, 1972.

    Google Scholar 

  13. Grossfeld H: Production of hyaluronic acid in tissue culture of Rous sarcoma. Nature 196:782–783, 1962.

    Google Scholar 

  14. Glimelius B, Norling B, Westermark B, Wasteson A: Composition and distribution of glycosaminoglycans in cultures of human normal and malignant glial cells. Biochem J 172:443–456, 1977.

    Google Scholar 

  15. Luft JH: Ruthenium red and violet. I. Chemistry, purification, methods of use for electron microscopy and mechanism of action. Anat Rec 171:347–368, 1971.

    Google Scholar 

  16. Behnke O, Zelander T: Preservation of intercellular substances by the cationic dye Alcian blue in preparative procedures for electron microscopy. J Ultrastructure Res 31:424–438, 1970.

    Google Scholar 

  17. Del Guidice RA, Hopps HE: Microbiological methods and fluorescent microscopy for the direct demonstration of mycoplasma infection of cell cultures. In: McGarrity GI, Murphy DG, Nicols WW (eds) Mycoplasma infection of cell cultures. Plenum Press, New York, 1976, pp 57–69.

    Google Scholar 

  18. Winter WT, Smith PJC, Arnott S: Hyaluronic acid. Structure of a fully extended 3-fold helical sodium salt and comparison with the less extended 4-fold helical form. J Mol Biol 99:219–235, 1975.

    Google Scholar 

  19. Guss JM, Huken PWL, Smith PJC, Winter WT, Pirnott S, Moorhouse R, Rees DA: Hyaluronic acid molecular conformations and interactions in 2 sodium salts. J Mol Biol 95:359–384, 1975.

    Google Scholar 

  20. Ogston AG, Phelps CF: The partition of solutes between buffer solutions and solutions containing hyaluronic acid. Biochem J 78:827–833, 1960.

    Google Scholar 

  21. Yamada J, Kennedy DW, Kimata J, Pratt RM: Characterization of fibronectin interactions with glycosaminoglycans and identification of active proteolytic fragments. J Biol Chem 255:6055–6063, 1980.

    Google Scholar 

  22. Hiramota R, Bernecky J, Jurandowski J, Pressman D: Fibrin in human tumors. Cancer Res 20:592–593, 1960.

    Google Scholar 

  23. Dvorak HF, Dvorak AM, Manseau EJ, Wiberg L, Churchill WH: Fibrin gel investment associated with line 1 and line 10 solid tumor growth, angiogenesis, and fibroplasia in guinea pigs. Role of cellular immunity, myobibroblasts, microvascular damage and infarction in line 1 tumor regression. JNCI 62:1459–1472, 1979.

    Google Scholar 

  24. Dorfman A, Ho PL: Synthesis of mucopolysaccharides by glial tumor cells in tissue culture. Proc Natl Acad Sci USA 66:495–499, 1970.

    Google Scholar 

  25. Culp LA, Ansbacher R, Domen C: Adhesion sites of neural tumor cells biochemical composition. Biochemistry 19:5899–5907, 1980.

    Google Scholar 

  26. Earle KM: Histochemistry of brain tumors. A study of the PAS positive substances in 486 intracranial neoplasms and 30 intraspinal neoplasms. Lab Invest 8:665–679, 1959.

    Google Scholar 

  27. Bock P, Jellinger K: Detection of glycosaminoglycans in human gliomas by histochemical methods. Acta Neuropathol (Berl.) Suppl VII:181, 1981.

    Google Scholar 

  28. Engelhardt A: Detection of acid mucopolysaccharides in brain tumors by histochemical methods. Acta Neuropathol (Berl.) 49:199–203, 1980.

    Google Scholar 

  29. Anderson DR, Spencer WH: Ultrastructural and histochemical observations of optic nerve gliomas. Arch Ophthal 83:324–335, 1970.

    Google Scholar 

  30. Arseni C, Carp N, Mestes E, Adel M: Histochemistry of mucopolysaccharides in brain tumors. Acta Neuropathol (Berl.) Suppl VII:275–284, 1981.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Oberc-Greenwood, M.A., Muul, L.M., Gately, M.K. et al. Ultrastructural features of the lymphocyte-stimulated halos produced by human glioma-derived cells in vitro . J Neuro-Oncol 3, 387–396 (1986). https://doi.org/10.1007/BF00165589

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00165589

Keywords

Navigation