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British Journal of Cancer logoLink to British Journal of Cancer
. 1980 Nov;42(5):722–729. doi: 10.1038/bjc.1980.307

Factors inducing a loss of net negative surface charge on spleen cells of mice grafted with a slow-growing tumour.

D Vaillier, J Vaillier
PMCID: PMC2010537  PMID: 7459209

Abstract

The mean electrophoretic mobility (EPM) of splenic cells was determined in 4 different host-tumour systems. In splenic cells harvested from mice bearing slow-growing tumours, a significant EPM decrease was observed (12%) and in increase in the proportion of cells with slow mobility. Moreover, after 1 h incubation in RPMI medium at 37 degrees C and 2 washings, spleen cells showed a marked increase in their EPM (average 30%). Finally, the supernatant from incubation medium after contact with normal spleen cells (1 h at 37 degrees C) produced a significant decrease in their EPM (approximately 12%). On the other hand, no significant EPM variations were found between control spleen cells and cells from fast-growing tumours, before or after 1h incubation. The existence of factors which induce a loss of negative surface charge on spleen cells of some tumour-grafted mice is discussed.

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Selected References

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

  1. Arnaiz-Villena A., Jones B., Roitt I. M. Allograft cytotoxicity. Role of T lymphocytes bearing a receptor for complement. Immunology. 1975 Nov;29(5):903–908. [PMC free article] [PubMed] [Google Scholar]
  2. BANGHAM A. D., HEARD D. H., FLEMANS R., SEAMAN G. V. An apparatus for microelectrophoresis of small particles. Nature. 1958 Sep 6;182(4636):642–644. doi: 10.1038/182642a0. [DOI] [PubMed] [Google Scholar]
  3. Dorizzi M., Ortiz-Muniz G., Lopez D. M., Sigel M. M., Epstein R. S. Increase in the proportion of cells with the C'3 receptor in BALB/c mice bearing mammary tumors. Int J Cancer. 1975 Dec 15;16(6):1015–1021. doi: 10.1002/ijc.2910160615. [DOI] [PubMed] [Google Scholar]
  4. Dular U., Chow D. A., Paraskevas F. Surface membrane changes of T cells induced by syngeneic tumour cells. I. Formation and uptake of complexes of Ig and tumour antigens by T cells. Int J Cancer. 1978 Nov 15;22(5):611–620. doi: 10.1002/ijc.2910220517. [DOI] [PubMed] [Google Scholar]
  5. Epstein R. S., Lopez D. M., Ortiz-Muniz G., Sigel M. M. Emergence of a subpopulation of lymphocytes bearing theta antigen and complement receptor during tumor growth. Int J Cancer. 1976 Oct 15;18(4):458–461. doi: 10.1002/ijc.2910180410. [DOI] [PubMed] [Google Scholar]
  6. Galili U., Häyry P., Klein E. Loss of net negative surface charge during MLC stimulation of human T lymphocytes: correlation to "stable" E-rosette formation and natural attachment to normal and malignant target cells. Cell Immunol. 1979 Nov;48(1):91–99. doi: 10.1016/0008-8749(79)90102-3. [DOI] [PubMed] [Google Scholar]
  7. Jenkins R. Distribution of electrophoretic mobilities of mouse thymocyte subpopulations in the presence of tumour cells. Immunology. 1975 Nov;29(5):893–902. [PMC free article] [PubMed] [Google Scholar]
  8. Kontiainen S., Mitchison N. A. Blocking antigen-antibody complexes on the T-lymphocyte activation during in vitro incubation before adoptive transfer. Immunology. 1975 Mar;28(3):523–533. [PMC free article] [PubMed] [Google Scholar]
  9. Mitchell D. M., Cater D. B. The electrophoretic mobility of BP8 ascites tumour cells and allergized lymph-node cells after treatment with inflammatory mediators, ptomaines, polyamines, antisera and neuraminidase or heparin. Br J Exp Pathol. 1971 Apr;52(2):152–171. [PMC free article] [PubMed] [Google Scholar]
  10. Ross G. D., Rabellino E. M., Polley M. J., Grey H. M. Combined studies of complement receptor and surface immunoglobulin-bearing cells and sheep erythrocyte rosette-forming cells in normal and leukemic human lymphocytes. J Clin Invest. 1973 Feb;52(2):377–385. doi: 10.1172/JCI107194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ruhenstroth-Bauer G., Lücke-Huhle C. Two populations of small lymphocytes. J Cell Biol. 1968 Apr;37(1):196–199. doi: 10.1083/jcb.37.1.196. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Suemura M., Kishimoto T., Hirai Y., Yamamura Y. Regulation of antibody response in different immunoglobulin classes. III. In vitro demonstration of "IgE class-specific" suppressor functions of DNP-mycobacterium-primed T cells and the soluble factor released from these cells. J Immunol. 1977 Jul;119(1):149–155. [PubMed] [Google Scholar]
  13. Treves A. J., Cohen I. R., Feldman M. Suppressor factor secreted by T-lymphocytes from tumor-bearing mice. J Natl Cancer Inst. 1976 Aug;57(2):409–414. doi: 10.1093/jnci/57.2.409. [DOI] [PubMed] [Google Scholar]
  14. Vaillier D., Vaillier J., Bischoff P. Relationship between tumour growth rate and proteic variations in interstitial subcutaneous fluid and serum: possible thymic control. Eur J Cancer. 1977 Sep;13(9):1025–1032. doi: 10.1016/0014-2964(77)90182-7. [DOI] [PubMed] [Google Scholar]
  15. Wioland M., Sabolovic D., Burg C. Electrophoretic mobilities of T and B cells. Nat New Biol. 1972 Jun 28;237(78):274–276. doi: 10.1038/newbio237274a0. [DOI] [PubMed] [Google Scholar]
  16. Zeiller K., Pascher G. Detection of T and B cell-specific heteroantigens on electrophoretically separated lymphocytes of the mouse. Eur J Immunol. 1973 Oct;3(10):614–618. doi: 10.1002/eji.1830031004. [DOI] [PubMed] [Google Scholar]

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