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Distribution of anti-Leu-7, anti-Leu-11a and anti-Leu-M1 immunoreactivity in the brain of the adult rat

Summary

This study reports a specific cross-reactivity of the three anti-human-hematopoetic-cell monoclonal antibodies, anti-Leu-7 (HNK-1), anti-Leu-11a (NKP-15), and anti-Leu-M1 (MMA), with different epitopes in the brain of the adult rat. The distribution of these epitopes in rat brain is determined by means of immunohistochemistry in paraffin-embedded frontal serial sections.

The reaction pattern of anti-Leu-11a monoclonal antibody is very similar to that of polyclonal antibodies against the myelin basic protein. Both antisera give a specific reaction with myelinated fibers. Immunoreaction products with the anti-Leu-7 monoclonal antibody are found as diffuse, mostly punctiform material in the neuropil and even more evident as small granules coating the cell surface of many neurons. In the white matter anti-Leu-7 reveals a moderate reactivity, which occurs predominantly as spots and fine-stranded material within the myelinated fiber tracts.

Anti-Leu-M1 immunoreactivity is present between myelinated fiber bundles of the white matter, where it has a reticulate appearance, and as fine-granulated material within the grey matter of the cortex and the nuclei. The characteristic feature in the grey matter is that of irregularly shaped immunopositive plaques, which are often located around small blood vessels. The cytoplasm of glial and neuronal cells appeared negative with this MAB.

The exact topographical distribution of the Leu-7 and Leu-M1 epitopes throughout the rat brain is described. The present hypotheses concerning the nature of this shared antigenicity between hematopoetic cells and nervous tissue are discussed.

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References

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

    Google Scholar 

  • Barclay AN (1978) Localization of the Thy-1 antigen in the cerebellar cortex of the rat brain by immunofluorescence during postnatal development. J Neurochem 32:1249–1257

    Google Scholar 

  • Barclay AN, Hyden H (1978) Localization of the Thy-1 antigen in the rat brain and spinal cord by immunofluorescence. J Neurochem 31:1375–1391

    Google Scholar 

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

    Google Scholar 

  • Carrel S, de Tribolet N, Groos N (1982) Expression of HLA-DR and common acute lymphoblastic leukemia antigens on glioma cells. Eur J Immunol 12:354–357

    Google Scholar 

  • Crawford JM, Barton RW (1986) Biology of disease — Thy-1 glycoprotein: Structure, distribution, and ontogeny. Lab Invest 54:122–135

    Google Scholar 

  • Dales S, Fujinami RS, Oldstone MBA (1983) Serologic relatedness between Thy-1,2 and actin revealed by monoclonal antibody. J Immunol 131:1332–1338

    Google Scholar 

  • Dulbecco R, Unger M, Bologna M, Battifora H, Syka P, Okada S (1981) Cross-reactivity between Thy-1 and a component of intermediate filaments demonstrated using a monoclonal antibody. Nature 292:772–774

    Google Scholar 

  • Fallon JH (1983) The island of Calleja complex of the rat basal forebrain connections of medium and large sized cells. Brain Res Bull 10:775–793

    Google Scholar 

  • ffrench-Constant C, Miller RH, Kruse J, Schachner M, Raff MC (1986) Molecular specialization of astrocyte processes at nodes of Ranvier in rat optic nerve. J Cell Biol 102:844–852

    Google Scholar 

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

    Google Scholar 

  • 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 

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

    Google Scholar 

  • Hauser SL, Bhan AK, Gilles FH, Hoban CJ, Reinherz EL, Schlossman SF, Weiner HL (1983) Immunohistochemical staining of human brain with monoclonal antibodies that identify lymphocytes, monocytes, and the Ia antigen. J Neuroimmunol 5:197–205

    Google Scholar 

  • Hawkes R, Colonier M, Lecler N (1985) Monoclonal antibodies reveal sagittal banding in the rodent cerebellar cortex. Brain Res 333:359–365

    Google Scholar 

  • Kemshead JT, Bicknell D, Greaves MF (1981) A monoclonal antibody detecting an antigen shared by neural and granulocytic cells. Pediatr Res 15:1282–1286

    Google Scholar 

  • Krusc 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 

  • Kruse J, Keilhauer G, 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 

  • Kubagawa H, Abo T, Balch CM, Cooper MD (1983) Biochemical analysis of antigenic determinants recognized on human natural killer cells by HNK-1 (Leu-7) antibody. Fed Proc Abstr 42:1219

    Google Scholar 

  • McGarry RC, Helfand SL, Quarles RH, Roder JC (1983) Recognition of myelin-associated glycoprotein by the monoclonal antibody HNK-1. Nature 306:376–378

    Google Scholar 

  • Murray N, Steck AJ (1984) Indication of a possible role in a demyelinating neuropathy for an antigen shared between myelin and NK cells. Lancet, March 31 (1984):711–712

    Google Scholar 

  • Natali PG, de Martino C, Quaranta V, Nicotra MR, Frezza F, Pelegrino MA, Ferrone S (1981) Expression of Ia-like antigen in normal human nonlymphoid tissues. Transplantation 31:75–78

    Google Scholar 

  • Niedick B, Löhler J (1986) Comparative studies on the cross-reaction of anti-human leucocyte monoclonal antibodies MMA and HNK-1 with oligodendrocytes in vitro. Clin Neuropathol Abstr 5(3):125

    Google Scholar 

  • Perussia B, Trinchieri G, Jackson A, Warner NL, Faust J, Rumpold H, Kraft D, Lanier LL (1984) The Fc receptor for IgG on human natural killer cells: Phenotypic, functional, and comparative studies with monoclonal antibodies. J Immunol 133:180–189

    Google Scholar 

  • Phillips JH, Babcock GF (1983) NKP-15: A monoclonal antibody reactive against purified human natural killer cells and granulocytes. Immunol Lett 6:143

    Google Scholar 

  • Plioplys AV, Thibault J, Hawkes R (1985) Selective staining of a subset of Purkinje cells in the human cerebellum with monoclonal antibody mabQ113. J Neurol Sci 70:245–256

    Google Scholar 

  • Poppema S, Bhan AK, Reinherz EL, McCluskay R, Schlossmann SF (1981) Distribution of T-cell subsets in human lymph nodes. J Exp Med 153:30–41

    Google Scholar 

  • Reif AE, Allen JMV (1964) The AKR thymic antigen and its distribution in leukemias and nervous tissues. J Exp Med 120:413–433

    Google Scholar 

  • Rotter A (1984) Cholinergic receptors. In: Björklund A, Hökfelt T (eds) Handbook of Chemical Neuroanatomy. Elsevier Amsterdam, Vol 3, pp 273–303

    Google Scholar 

  • Schuller-Petrovic S, Gebhardt 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 

  • Sternberger LA (1979) Immunocytochemistry. 2nd edition, John Wiley and Sons, New York

    Google Scholar 

  • Stoll G, Schwendemann G, Heininger K, Steck AJ, Toyka KV (1985) Human monoclonal anti-MAG antibody and anti-Leu-7 recognize shared antigenic determinants in peripheral nerve and spinal cord. J Neurol Neurosurg Psychiatry 48:635–638

    Google Scholar 

  • Wernecke H, Lindner J, Schachner M (1985) Cell type specificity and developmental expression of the L2/HNK-1 epitopes in mouse cerebellum. J Neuroimmunol 9:115–130

    Google Scholar 

  • Zilles K (1985) The cortex of the rat — A stereotactic atlas. Springer, Berlin Heidelberg New York Tokyo

    Google Scholar 

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Supported by the Deutsche Forschungsgemeinschaft, SFB 200

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Reifenberger, G., Mai, J.K., Krajewski, S. et al. Distribution of anti-Leu-7, anti-Leu-11a and anti-Leu-M1 immunoreactivity in the brain of the adult rat. Cell Tissue Res. 248, 305–313 (1987). https://doi.org/10.1007/BF00218197

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  • DOI: https://doi.org/10.1007/BF00218197

Key words

  • Brain
  • Immunohistochemistry
  • Natural killer cells
  • Monocytes
  • Granulocytes
  • Rat