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. 1980 May;77(5):2895–2898. doi: 10.1073/pnas.77.5.2895

Natural cytotoxic cells against solid tumors in mice: blocking of cytotoxicity by D-mannose.

O Stutman, P Dien, R E Wisun, E C Lattime
PMCID: PMC349512  PMID: 6930673

Abstract

Natural cytotoxic (NC) and natural killer (NK) cells have been defined by their ability to lyse certain solid or lymphoid tumor targets in vitro, without prior sensitization. Our present studies describe an attempt to characterize the structures involved in the effector-target recognition leading to tumor cell lysis. Addition of the monosaccharide D-mannose to the NC cell assay significantly blocked cytotoxicity of the fibrosarcoma Meth A target by the effector cells at 50 mM and lower concentrations. D-Galactose showed blocking activity in one of five experiments, only at 50 mM. L-Fucose, D-glucose, and N-acetyl-D-glucosamine did not affect NC cell cytotoxicity at similar concentrations. All of the sugars tested inhibited NK cell lysis of the lymphoma YAC-I target. None of the sugars affected killing of the appropriate target by allosensitized cytotoxic T lymphocytes. The blocking of NC-mediated cytotoxicity was not due to a direct toxic action of the sugars on the effector cells. These findings suggest that, in the NC system, recognition involves lectin-like structures with a specificity for D-mannose (or D-galactose, or both), whereas, in the NK system, such lectin-like structures are less restricted. Such structures appear not to be involved in the specific cytotoxicity mediated by T cells.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Balsamo J., Lilien J. The binding of tissue-specific adhesive molecules to the cell surface. A molecular basis for specificity. Biochemistry. 1975 Jan 14;14(1):167–171. doi: 10.1021/bi00672a028. [DOI] [PubMed] [Google Scholar]
  2. Bar-Shavit Z., Ofek I., Goldman R., Mirelman D., Sharon N. Mannose residues on phagocytes as receptors for the attachment of Escherichia coli and Salmonella typhi. Biochem Biophys Res Commun. 1977 Sep 9;78(1):455–460. doi: 10.1016/0006-291x(77)91276-1. [DOI] [PubMed] [Google Scholar]
  3. Besancon F., Ankel H., Basu S. Specificity and reversibility of interferon ganglioside interaction. Nature. 1976 Feb 19;259(5544):576–578. doi: 10.1038/259576a0. [DOI] [PubMed] [Google Scholar]
  4. Brown R. C., Bass H., Coombs J. P. Carbohydrate binding proteins involved in phagocytosis by Acanthamoeba. Nature. 1975 Apr 3;254(5499):434–435. doi: 10.1038/254434a0. [DOI] [PubMed] [Google Scholar]
  5. GELB L. D., LERNER A. M. REOVIRUS HEMAGGLUTINATION: INHIBITION BY N-ACETYL-D-GLUCOSAMINE. Science. 1965 Jan 22;147(3656):404–405. doi: 10.1126/science.147.3656.404. [DOI] [PubMed] [Google Scholar]
  6. Gartner T. K., Williams D. C., Minion F. C., Phillips D. R. Thrombin-induced platelet aggregation is mediated by a platelet plasma membrane-bound lectin. Science. 1978 Jun 16;200(4347):1281–1283. doi: 10.1126/science.663608. [DOI] [PubMed] [Google Scholar]
  7. Gesner B., Thomas L. Sialic acid binding sites: role in hemagglutination by Mycoplasma gallisepticum. Science. 1966 Feb 4;151(3710):590–591. doi: 10.1126/science.151.3710.590. [DOI] [PubMed] [Google Scholar]
  8. Grabel L. B., Rosen S. D., Martin G. R. Teratocarcinoma stem cells have a cell surface carbohydrate-binding component implicated in cell-cell adhesion. Cell. 1979 Jul;17(3):477–484. doi: 10.1016/0092-8674(79)90255-1. [DOI] [PubMed] [Google Scholar]
  9. Hatanaka M. Sugar effects on murine sarcoma virus transformation. Proc Natl Acad Sci U S A. 1973 May;70(5):1364–1367. doi: 10.1073/pnas.70.5.1364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hatanaka M. Transport of sugars in tumor cell membranes. Biochim Biophys Acta. 1974 Apr 29;355(1):77–104. doi: 10.1016/0304-419x(74)90008-0. [DOI] [PubMed] [Google Scholar]
  11. Hausman R. E., Moscona A. A. Purification and characterization of the retina-specific cell-aggregating factor. Proc Natl Acad Sci U S A. 1975 Mar;72(3):916–920. doi: 10.1073/pnas.72.3.916. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Herberman R. B., Djeu J., Kay H. D., Ortaldo J. R., Riccardi C., Bonnard G. D., Holden H. T., Fagnani R., Santoni A., Puccetti P. Natural killer cells: characteristics and regulation of activity. Immunol Rev. 1979;44:43–70. doi: 10.1111/j.1600-065x.1979.tb00267.x. [DOI] [PubMed] [Google Scholar]
  13. Herberman R. B., Holden H. T. Natural cell-mediated immunity. Adv Cancer Res. 1978;27:305–377. doi: 10.1016/s0065-230x(08)60936-7. [DOI] [PubMed] [Google Scholar]
  14. Kalckar H. M. Galactose metabolism and cell "sociology". Science. 1965 Oct 15;150(3694):305–313. doi: 10.1126/science.150.3694.305. [DOI] [PubMed] [Google Scholar]
  15. Kemp A. S., Berke G., Dawson J. R., Amos D. B. The influence of normal serum components on lymphocyte-mediated cytolysis in vitro. Transplantation. 1974 May;17(5):447–452. doi: 10.1097/00007890-197405000-00002. [DOI] [PubMed] [Google Scholar]
  16. Kiessling R., Wigzell H. An analysis of the murine NK cell as to structure, function and biological relevance. Immunol Rev. 1979;44:165–208. doi: 10.1111/j.1600-065x.1979.tb00270.x. [DOI] [PubMed] [Google Scholar]
  17. Lattime E. C., Gershon H. E., Stutman O. Allogeneic radiation chimeras respond to TNP-modified donor and host targets. J Immunol. 1980 Jan;124(1):274–278. [PubMed] [Google Scholar]
  18. Linna T. J., Engers H. D., Cerottini J. C., Brunner K. T. Inhibition of cytolytic T lymphocyte activity with subcellular alloantigen preparations and with unlabeled allogeneic target cells. J Immunol. 1978 May;120(5):1544–1549. [PubMed] [Google Scholar]
  19. Lis H., Sharon N. The biochemistry of plant lectins (phytohemagglutinins). Annu Rev Biochem. 1973;42(0):541–574. doi: 10.1146/annurev.bi.42.070173.002545. [DOI] [PubMed] [Google Scholar]
  20. Martz E. Mechanism of specific tumor-cell lysis by alloimmune T lymphocytes: resolution and characterization of discrete steps in the cellular interaction. Contemp Top Immunobiol. 1977;7:301–361. doi: 10.1007/978-1-4684-3054-7_9. [DOI] [PubMed] [Google Scholar]
  21. Muramatsu T., Gachelin G., Damonneville M., Delarbre C., Jacob F. Cell surface carbohydrates of embryonal carcinoma cells: polysaccharidic side chains of F9 antigens and of receptors to two lectins, FBP and PNA. Cell. 1979 Sep;18(1):183–191. doi: 10.1016/0092-8674(79)90367-2. [DOI] [PubMed] [Google Scholar]
  22. Nicolson G. L. Trans-membrane control of the receptors on normal and tumor cells. II. Surface changes associated with transformation and malignancy. Biochim Biophys Acta. 1976 Apr 30;458(1):1–72. doi: 10.1016/0304-419x(76)90014-7. [DOI] [PubMed] [Google Scholar]
  23. Ofek I., Mirelman D., Sharon N. Adherence of Escherichia coli to human mucosal cells mediated by mannose receptors. Nature. 1977 Feb 17;265(5595):623–625. doi: 10.1038/265623a0. [DOI] [PubMed] [Google Scholar]
  24. Paige C. J., Figarella E. F., Cuttito M. J., Cahan A., Stutman O. Natural cytotoxic cells against solid tumors in mice. II. Some characteristics of the effector cells. J Immunol. 1978 Nov;121(5):1827–1835. [PubMed] [Google Scholar]
  25. Roder J. C., Kiessling R., Biberfeld P., Andersson B. Target-effector interaction in the natural killer (NK) cell system. II. The isolation of NK cells and studies on the mechanism of killing. J Immunol. 1978 Dec;121(6):2509–2517. [PubMed] [Google Scholar]
  26. Roder J. C., Kiessling R. Target--effector interaction in the natural killer cell system. I. Covariance and genetic control of cytolytic and target-cell-binding subpopulations in the mouse. Scand J Immunol. 1978;8(2):135–144. doi: 10.1111/j.1365-3083.1978.tb00505.x. [DOI] [PubMed] [Google Scholar]
  27. Roder J. C., Rosén A., Fenyö E. M., Troy F. A. Target-effector interaction in the natural killer cell system: isolation of target structures. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1405–1409. doi: 10.1073/pnas.76.3.1405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Stutman O., Paige C. J., Figarella E. F. Natural cytotoxic cells against solid tumors in mice. I. Strain and age distribution and target cell susceptibility. J Immunol. 1978 Nov;121(5):1819–1826. [PubMed] [Google Scholar]
  29. Vacquier V. D., Moy G. W. Isolation of bindin: the protein responsible for adhesion of sperm to sea urchin eggs. Proc Natl Acad Sci U S A. 1977 Jun;74(6):2456–2460. doi: 10.1073/pnas.74.6.2456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Vicker M. G. BHK21 fibroblast aggregation inhibited by glycopeptides from the cell surface. J Cell Sci. 1976 Jun;21(1):161–173. doi: 10.1242/jcs.21.1.161. [DOI] [PubMed] [Google Scholar]

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