Skip to main content

Expression of 3-fucosyl-N-acetyllactosamine on glia cells and its putative role in cell adhesion

Summary

Mouse monoclonal antibodies from five clones (MMA, 1G10, VIM C6, MC-1 and Tü9), elicited to human myeloid cells and reactive with the 3-fucosyl-N-acetyllactosamine sequence (also termed X-determinant), cross-react with glia cells from human and rat brain. In brain cell cultures from neonatal rats both astrocytes and oligodendrocytes express the X-determinant during the first period of the culture as shown by immunofluorescence tests. While the astrocytes, which exhibit signs of adhesion, permanently express the X-determinant, the oligoden-drocytes lose the epitope nearly completely during culture. The oligodendrocytes preferentially grow on top of the astrocytic layer. After about 8–10 days of culture, numerous X-determinant-positive astrocytic membranes show oligodendrocyte-shaped negative print images underneath the galactocerebroside-positive oligodendrocytes. At this time, the oligodendrocytes are relatively firmly attached to the astrocytic layer. Since participation of the X-determinant in the compaction of the mouse 8–32 cell stage is being discussed, we conclude from our observations that the X-determinant may also play a role in the astrocyte-astrocyte and astrocyte-oligodendrocyte adhesion. It may represent the functionally active carbohydrate moiety of a heterotypic cell adhesion molecule of glia cells.

This is a preview of subscription content, access via your institution.

References

  1. Abo T, Balch CM (1981) A differentiation antigen of human NK and K cells identified by a monoclonal antibody (HNK-1). J Immunol 127:1024–1029

    Google Scholar 

  2. Barnstable CJ, Bodmer WF, Brown, G, Galfre G, Milstein C, Williams AF, Ziegler A (1978) Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens. New tools for genetic analysis. Cell 14:9–20

    Google Scholar 

  3. Bird JM, Kimber SJ (1984) Oligosaccharides containing fucose-linked α(1–3) and α(1–4) toN-acetylglucosamine cause decompaction of mouse morulae. Dev Biol 104:449–460

    Google Scholar 

  4. Budka H, Majdic O (1985) Shared antigenic determinants between human hemopoietic cells and nervous tissues and tumors. Acta Neuropathol (Berl) 67:58–66

    Google Scholar 

  5. Crawford JM, Barton RW (1986) Thy-1 glycoprotein: structure, distribution and ontogeny. Lab Invest 54:122–135

    Google Scholar 

  6. Edelman GM (1983) Cell adhesion molecules. Science 219:450–457

    Google Scholar 

  7. Fox N, Damjanow I, Knowles BB, Solter D (1983) Immuno-histochemical localization of the mouse stage-specific embryonic antigen 1 in human tissues and tumors. Cancer Res 43:669–678

    Google Scholar 

  8. Fuchs S, Schmidt-Hopfeld I, Tridente G, Tarrab-Hazdai R (1980) Thymic lymphocytes bear a surface antigen which cross-reacts with acetylcholine receptor. Nature 287:162–164

    Google Scholar 

  9. Garson JA, Beverley PCL, Coakham HB, Harper EI (1982) Monoclonal antibodies against human T lymphocytes label Purkinje neurons of many species. Nature 298:375–377

    Google Scholar 

  10. Gooi HC, Feizi T, Kapadia A, Knowles BB, Solter D, Evans MJ (1981) Stage-specific embryonic antigen involves α1→3 fucosylated type 2 blood group chains. Nature 292:156–158

    Google Scholar 

  11. Graham RC, Karnovsky MJ (1966) The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem 14:291–298

    Google Scholar 

  12. Greaves MF, Chan LC, Furley AJW, Watt SM, Molgaard HV (1986) Lineage promiscuity in hematopoietic differentiation and leukemia. Blood 67:1–11

    Google Scholar 

  13. Hanjan SNS, Kearney JF, Cooper MD (1982) A monoclonal antibody (MMA) that identifies a differentiation antigen on human myelomonocytic cells. Clin Immunol Immunopathol 23:172–188

    Google Scholar 

  14. Hsu SM, Raine L, Fanger H (1981) Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques. A comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem 9:577–580

    Google Scholar 

  15. Hsu SM, Jaffe ES (1984) Leu M 1 and peanut agglutinin stain the neoplastic cells of Hodgkin's disease. Am J Clin Pathol 82:29–32

    Google Scholar 

  16. Kerr MA, McCarthy NC (1985) A carbohydrate differentiation antigen of granulocytes, brain and many tumors. Biochem Soc Trans 13:424–426

    Google Scholar 

  17. Kruse J, Mailhammer R, Wernecke H, Faissner A, Sommer I, Goridis C, Schachner M (1984) Neural cell adhesion molecules and myelin-associated glycoprotein share a common carbohydrate moiety recognized by monoclonal antibodies L2 and HNK-1. Nature 311:153–155

    Google Scholar 

  18. Kruse J, Keilhauer G, Faissner A, Timpl R, Schachner M (1985) The J1 glycoprotein — a novel nervous system cell adhesion molecule of the L2/HNK-1 family. Nature 316:146–148

    Google Scholar 

  19. Lagenaur C, Schachner M, Solter D, Knowles BB (1982) Monoclonal antibody to SSEA-1 is specific for a subpopulation of astrocytes in mouse cerebellum. Neurosci Lett 31:181–184

    Google Scholar 

  20. Levinthal JD, Dunnebacke TH, Williams RC (1969) Study of poliovirus infection of human and monkey cells by indirect immunoferritin technique. Virology 39:211–223

    Google Scholar 

  21. Majdic O, Bettelheim P, Stockinger H, Aberer W, Lizka K, Lutz D, Knapp W (1984) Mz, a novel myelomonocytic cell surface antigen and its distribution on leukemic cells. Int J Cancer 33:617–623

    Google Scholar 

  22. Mason DY, Woolston R-E (1982) Double immuno-enzymatic labelling. In: Bullock GR, Petrusz P (eds) Techniques in immunocytochemistry, vol 1. Academic Press. London, pp 135–153

    Google Scholar 

  23. McCarthy KD, de Vellis J (1980) Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue. J Cell Biol 85:890–902

    Google Scholar 

  24. Niedieck B (1975) On a glycolipid hapten of myelin. Prog Allergy 18:353–422

    Google Scholar 

  25. Raff MC, Fields KL, Hakomori S, Mirsky R, Pruss RM, Winter J (1979) Cell type-specific markers for distinguishing and studying neurons and the major classes of glia cells in culture. Brain Res 174:283–308

    Google Scholar 

  26. Reif AE, Allen JMV (1964) The AKR thymic antigen and its distribution in leukemias and nervous tissues. J Exp Med 120:413–435

    Google Scholar 

  27. Schuller-Petrovic S, Gebhart W, Lassmann H, Rumpold H, Kraft D (1983) A shared antigenic determinant between natural killer cells and nervous tissue. Nature 306:179–181

    Google Scholar 

  28. Schwarting GA, Jungalwala FB, Chou DKH, Boyer AM, Yamamoto M (1987) Sulfated glucoronic acid-containing glycoconjugates are temporally and spatially regulated antigens in the developing mammalian nervous system. Dev Biol 120:65–76

    Google Scholar 

  29. Solter D, Knowles BB (1978) Monoclonal antibody defining a stage-specific mouse embryonic antigen (SSEA-1). Proc Natl Acad Sci USA 75:5565–5569

    Google Scholar 

  30. Spiro RG (1966) Characterization of carbohydrate units of glycoproteins. Methods Enzymol 8:26–52

    Google Scholar 

  31. Stockinger H, Majdic O, Liszka K, Aberer W, Bettelheim P, Lutz D, Knapp W (1984) Exposure by desialylation of myeloid antigens on acute lymphoblastic leukemia cells. J Natl Cancer Inst 73:7–11

    Google Scholar 

  32. Thompson JS, Gocken NE, Brown SA, Rhoades JL (1982) Phenotypic definition of human monocyte/macrophage subpopulations by monoclonal antibodies. II. Distinction of non-T, non-B natural killer cells (NK) from antigen-presenting stimulating cells in the mixed lymphocyte response (MLR). American Association of Clinical Histocompatibility Testing, 8th Annual Meeting abstracts, p A 23

  33. Uchánska-Ziegler B, Wernet P, Ziegler A (1981) Monoclonal antibodies against human lymphoid and myeloid antigens: AMML cells as immunogen. In: Knapp W (ed) Proceedings of Leukemia Marker Conference. Academic Press, London, pp 243–246

    Google Scholar 

  34. Urdal DL, Brentnall TA, Bernstein ID, Hakomori S (1983) A granulocyte reactive monoclonal antibody, 1G10, identifies the Gal β 1–4 (Fuc α1–3) GlcNAc (X-determinant) expressed in HL-60 cells on both glycolipid and glycoprotein molecules. Blood 62:1022–1026

    Google Scholar 

  35. Yamamoto M, Boyer AM, Schwarting GA (1985) Fucose-containing glycolipids are stage-and region-specific antigens in developing embryonic brain of rodents. Proc Natl Acad Sci USA 82:3045–3049

    Google Scholar 

Download references

Author information

Affiliations

Authors

Additional information

Supported by the Gemeinnützige Hertie-Stiftung, Frankfurt/Main. The Heinrich-Pette-Institut is financially supported by Freie und Hansestadt Hamburg and Bundesministerium für Jugend, Familie, Frauen und Gesundheit

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Niedieck, B., Löhler, J. Expression of 3-fucosyl-N-acetyllactosamine on glia cells and its putative role in cell adhesion. Acta Neuropathol 75, 173–184 (1987). https://doi.org/10.1007/BF00687079

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00687079

Key words

  • Brain cell culture
  • Glia cells
  • Immunolabeling
  • X-determinant
  • Cell adhesion molecule