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Natural cytotoxicity of rat hepatic natural killer cells and macrophages against a syngeneic colon adenocarcinoma

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Summary

The in vitro cytotoxic activity of two types of hepatic sinusoidal cells, i.e., natural killer (NK) cells and macrophages (Kupffer cells), was tested against a syngeneic rat colon adenocarcinoma cell line (DHD-K12). Purified hepatic NK cells (85% cells with large granular lymphocyte morphology) were spontaneously cytolytic, whereas Kupffer cells (90% pure) were not able to kill the DHD-K12 cells. This carcinoma cell line was found to be resistant to the action of mouse recombinant tumor necrosis factor which is considered as the major cytolytic molecule secreted by macrophages. However, colon carcinoma cells were readily lysed by soluble factors present in the culture supernatant of NK cells. It is postulated that hepatic NK cells, which are strategically located within the lumen of the sinusoids, may form a first line of defense to metastasizing colon carcinoma cells.

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References

  1. Bouwens L, Wisse E (1987) Immuno-electron microscopic characterization of large granular lymphocytes (natural killer cells) from rat liver. Eur J Immunol 17:1423

    Google Scholar 

  2. Bouwens L, Remels L, Baekeland M, Van Bossuyt H, Wisse E (1987) Large granular lymphocytes or pit cells from rat liver: isolation, ultrastructural characterization and natural killer activity. Eur J Immunol 17:37

    Google Scholar 

  3. Daemen T, Veninga A, Roerdink FH, Scherphof GL (1986) In vitro activation of rat liver macrophages to tumoricidal activity by free or liposome-encapsulated muramyl dipeptide. Cancer Res 46:4330

    Google Scholar 

  4. Decker T, Lohmann-Matthes ML, Gifford GE (1987) Cell-associated tumor necrosis factor (TNF) as a killing mechanism of activated cytotoxic macrophage. J Immunol 138:957

    Google Scholar 

  5. Fransen L, Van Der Heyden J, Ruysschaert R, Fiers W (1986) Recombinant tumor necrosis factor: its effect and its synergism with interferon-gamma on a variety of normal and transformed human cell lines. Eur J Cancer Clin Oncol 22:419

    Google Scholar 

  6. Introna M, Allavena P, Spreafico F, Mantovani A (1987) Inhibition of human natural killer activity by cyclosporin A. Transplantation 31:113

    Google Scholar 

  7. Jones EA, Summerfield JA (1982) Kupffer cells. In: The liver: biology and pathobiology. Raven Press, New York, p 507

    Google Scholar 

  8. Knook D, Blansjaar N, Sleyster E (1977) Isolation and characterization of Kupffer and endothelial cells from the rat liver. Exp Cell Res 109:317

    CAS  PubMed  Google Scholar 

  9. Lattime EC (1986) Natural cytotoxic activity: an introduction. Immunol Res 5:1

    Google Scholar 

  10. Lukomska B, Olszewski WL, Ziolkowska A, Engeset A (1984) Immunological characteristics of cells entering the liver with portal blood. Scand J Gastroenterol 8:1069

    Google Scholar 

  11. Malter M, Friedrich E, Suss R (1986) Liver as a tumor cell killing organ: Kupffer cells and natural killers. Cancer Res 46:3055

    Google Scholar 

  12. Martin MS, Martin F, Michiels R, Bastien H, Justrabo E, Bordes M, Viry B (1973) An experimental model for cancer of the colon and rectum: intestinal carcinoma induced in the rat by 1,2-dimethylhydrazine. Digestion 8:22

    Google Scholar 

  13. Ortaldo JR, Ransom JR, Sayers TJ, Herberman RB (1986) Analysis of cytostatic/cytotoxic lymphokines: relationship of natural killer cytotoxic factor to recombinant lymphotoxin, recombinant tumor necrosis factor, and leukoregulin. J Immunol 137:2857

    Google Scholar 

  14. Paige CJ, Figarella EF, Cuttito MJ, Stutman O (1978) Natural cytotoxic cells against solid tumors in mice. II. Some characteristics of the effector cells. J Immunol 137:2857

    Google Scholar 

  15. Pelletier H, Olsson NO, Shimizu T, Lagadec P, Fady C, Reisser D, Jeanin JF (1987) In vitro natural killer activity against progressive and regressive variants of a rat colon adenocarcinoma. Effect of treatments with anti-asialo GM1 plus complement. Immunobiology 175:202

    Google Scholar 

  16. Sherwood ER, Williams DL, McNamee RB, Jones EL, Browder IW, Diluzio NR (1987) In vitro tumoricidal activity of resting and glucan-activated Kupffer cells. J Leukocyte Biol 42:69

    Google Scholar 

  17. Van Bossuyt H, Wisse E (1988) Structural changes produced in Kupffer cells in the rat liver by injection of lipopolysaccharide. Cell Tissue Res 251:205

    Google Scholar 

  18. Van Der Elst J, De Greve J, Geerts F, De Neve W, Storme G, Willems G (1986) Quantitative study of liver metastases from colon cancer in rats after treatment with cyclosporin A. J Natl Cancer Inst 77:227

    Google Scholar 

  19. Wisse E (1974) Observations on the fine structure and peroxidase cytochemistry of normal rat liver Kupffer cells. J Ultrastruct Res 46:393

    Google Scholar 

  20. Wisse E, De Zanger R, Jacobs R (1983) Scanning EM observations on rat liver sinusoids relevant to microcirculation and transport processes. J Clin Electron Microscopy 16:427

    Google Scholar 

  21. Xu ZL, Bucana CD, Fidler IJ (1984) In vitro activation of murine Kupffer cells by lymphokines or endotoxins to lyse syngeneic tumor cells. Am J Pathol 117:372

    Google Scholar 

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Senior research assistant of the “National Fund for Scientific Research” (N.F.W.O., Belgium)

Supported by an A.S.L.K. cancer grant

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Bouwens, L., Jacobs, R., Remels, L. et al. Natural cytotoxicity of rat hepatic natural killer cells and macrophages against a syngeneic colon adenocarcinoma. Cancer Immunol Immunother 27, 137–141 (1988). https://doi.org/10.1007/BF00200018

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  • DOI: https://doi.org/10.1007/BF00200018

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