Enhancement of Lymphocyte Proliferation and Il-2 Receptor Expression by A Processed Form (Gm-1/P) of Monosialoganglioside GM-1

References

• Fishman P. H. Role of membrane gangliosides in the binding and action of bacteriol toxins. J. Membr. Biol. 1982; 69: 85
   PubMed Web of Science ®Google Scholar
• Markwell M. A.K., Svennerholm L., Paulson J. C. Specific gangliosides function as host cell receptors for Sendai virus. Proc. Natl. Acad. Sci. USA, 78: 5406, 981
   PubMedGoogle Scholar
• Bergelson L. D., Rukrinskaya A. G, Prokazova N. V., et al. Role of gangliosides in reception of influenza virus. Eur. J. Biochem. 1982; 128: 467
   PubMedGoogle Scholar
• Suzuki Y., Matsunaga M., Matsumoto M. N-Acetylneureminyl-lectosylceramide, GM3–NeuAc., a new influenza A virus receptor which mediates the adsorption-fusion process of viral infection. Binding specificity of influenza virus A/Aichi/2/68 (h3/N2) to membrane-associated GM3 with different molecule species of sialic acid. J. Biol. Chem., 260: 1362, 1985
   PubMedGoogle Scholar
• Real F. X., Houghton A. N., Albino A. P., Cordon -Cardo C., Melamed M. R., Oettgen H. F., Old C. J. Surface antigens of melanomas and melanocytes defined by mouse monoclonal antibodies: antigen expression in culture cells and tissues. Cancer Res., 45: 4401, 1985
   PubMedGoogle Scholar
• Cahan D. L., Lrie R., Singh R., Cassidenti A., Paulson J. C. Identification of a human neuroectodermal tumor antigen OFA-1–2 as ganglioside GD. Proc. Natl. Acad. Sci. USA 1982; 79: 7629
   PubMed Web of Science ®Google Scholar
• Pukel C., Lloyd K. O., Travassos L. R., Dippold W. G., Oettgen H. F., Old L. J. GD3 a prominent ganglioside of human melanoma. Detection and characterization by mouse monoclonal antibody. J. Exp. Med. 1982; 155: 31133
   Google Scholar
• Papsidero L. D., Nemoto T., Croghan G. A., Chu T. M. Expression of ductal carcinoma antigen in breast cancer sera as defined using monoclonal antibodies F36122. Cancer Res. 1984; 44: 4653
   PubMed Web of Science ®Google Scholar
• Cordon -Cardo C., Lloyd K. D., Sakamoto J., McGroarty M. E., Old L. J., Melamed M. R. Immunohistologic expression of blood group antigens in normal human gastrointestinal tract and colonic carcinoma. J. Cancer 1986; 37: 667
   Google Scholar
• Ferrari G., Fabris M., Gorio A. Gangliosides enhance neurite outgrowth in PC12 cells. Brain Res. 1983; 284: 215
   PubMedGoogle Scholar
• Tsuji S., Arita M., Nagai Y. G81b, a bioactive ganglioside that exhibits novel nerve growth factor (NGF)-like dctivitiee in two neuroblastoma cell lines. J. Biochem. 1983; 94: 303
   PubMedGoogle Scholar
• Bremer E. G., Hakomori S. GM3 ganglioside induces hamster fibroblast growth inhibition in chemically-defined medium: ganglioside may regulate growth factor receptor function. Biochem. Biophys. Res. Commun. 1982; 106: 711
   PubMedGoogle Scholar
• Hakornori S. Glycosphingolipids in cellular interaction, differentiation, and oncogenesis. Ann. Rev. Biochem. 1981; 50: 733
   PubMedGoogle Scholar
• Marcrw D. M. A review of the immunogenic and immunomodulatory properties of glycosphingolipids. Mol. Immunol. 1984; 21: 1083
   PubMedGoogle Scholar
• Krishnaraj R., Lin J., Kemp R. G. Lectin-and ionophore-stimulated Ca2+ influx in murine lymphocytes: inhibition by disialoganglioside. Cell Immunol. 1983; 78: 152
   PubMedGoogle Scholar
• Lengle E. E., Krishnaraj R., Kemp R. G. Inhibition of the lectin induced mitogenic response of thymocytes by glycolipids. Cancer Res. 1979; 39: 817
   PubMedGoogle Scholar
• Whisler R. L., Yates A. J. Regulation of lymphocyte responses by human gangliosides. J. Immnunol., 125: 2106, 1980
   PubMedGoogle Scholar
• Ladish S., Gillard B., Wong C., Ulsh L. Shedding and immunoregulatory activity of YAC-1 lymphoma cell gangliosides. Cancer Res., 43: 3808, 1983
   PubMedGoogle Scholar
• Marcus D. M., Dustira A., Diego I., Osovitz S, Lewis D E. Studies of the mechanisms by which gangliosides inhibit the proliferative response of murine splenocytes to Concanavalin A. Cell. Imunol. 1987; 104: 71
   PubMedGoogle Scholar
• Merrit W. D., Bailey J. M., Pluznik D. H. Inhibition of interleukin 2–dependent cytotoxic T-lymphocyte growth by gangliosides. Cell. Immunol. 1984; 89: 1
   PubMed Web of Science ®Google Scholar
• Parker J., Caldini G., Krishnamurti C., Ahrens P. B., Ankel H. Binding of interleukin-2 to gangliosides. FEBS 1984; 170: 391
   PubMedGoogle Scholar
• Robb R. J. The suppressive effect of gangliosides upon IL-2–dependent proliferation as a function of inhibition of IL-2 receptor association. J. Immunol. 1986; 136: 971
   PubMed Web of Science ®Google Scholar
• Jackson K. M., Yates A. J., Orosz C. G., Whitacre C. C. Gangliosides suppress the proliferation of autoreactive cells in experimental allergic encephalomyelitis: ganglioside effect on IL-2 activity. Cell. Immunol. 1987; 104: 169
   PubMedGoogle Scholar
• Spiegel S., Wilchek M. Membrane sialoglycolipids emerging ae possible signal transducers for lymphocyte etimulation. J. Immunol. 1981; 127: 572
   PubMedGoogle Scholar
• Welte K., Miller G., Chapman P. B., et al. Stimulation of T lymphocyte proliferation by monoclonal antibodies against GD3 ganglioside. J. Immunol. 1987; 139: 1763
   PubMed Web of Science ®Google Scholar
• Hersey P., Schibeci S. D., Townsend P., Burns C., Cheresh D. A. Potentiation of lymphocytes responses by monoclonal antibodies to the ganglioside GD. Cancer Res. 1984; 46: 6083
   Google Scholar
• Spiegel S., Fishman P. H., Weber R. J. Direct evidence that endogenous ganglioside can mediate thymocyte proliferation. Science 1985; 230: 1285
   PubMed Web of Science ®Google Scholar
• Santoni A., Piccoli M., Ortaldo J. R., Mason L., Wiltrout R. H., Herberman R. B. Changes in number and density of large granular lymphocytes on in vivo augmentation of mouse natural killer activity. J. Inununol. 1985; 134: 2799
   Google Scholar
• Julius M. H., Simpson E., Herzenberg L. A. A rapid method for the isolation of functional thymus derived murine lymphocytes. Eur. J. Immunol. 1973; 3: 645
   PubMed Web of Science ®Google Scholar
• Ceredig R., Lowenthal J. N., Nabholz M., McDonald R. Expression of interleukin-2 receptors as a differentiation marker of intrathymic stem cells. Nature 1985; 314: 98
   PubMed Web of Science ®Google Scholar
• Giuffrida A., Galli M. C., Gismondi A., et al. Augmentation of mouse natural killer (NK) activity by GM-l/P, a processed form of monosialogangliosf. de GM-1, Submitted for publication
   Google Scholar