The Control of IL-4 Gene Expression in Activated Murine T Lymphocytes: A Novel Role for neu-1 Sialidase

Journal of Immunology

Volumn 158, Issue 7, 1997, Pages 3070-3080

  Chen, Xiao Ping ^a   Enioutina, Elena Yu ^a   Daynes, Raymond A ^a,b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GANGLIOSIDE GM1; GANGLIOTETRAOSYLCERAMIDE; INTERLEUKIN 4; NEU1 PROTEIN, MOUSE; SIALIDASE;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; BIOSYNTHESIS; C3H MOUSE; C57BL MOUSE; CELL CULTURE; CYTOLOGY; DRUG ANTAGONISM; DRUG EFFECT; ENZYMOLOGY; FEMALE; GENE EXPRESSION REGULATION; GENETICS; IMMUNOLOGY; LYMPHOCYTE ACTIVATION; METABOLISM; MOUSE; PHYSIOLOGY; SPLEEN; T LYMPHOCYTE;

ANIMALS; CELLS, CULTURED; FEMALE; G(M1) GANGLIOSIDE; GENE EXPRESSION REGULATION; INTERLEUKIN-4; LYMPHOCYTE ACTIVATION; MICE; MICE, INBRED BALB C; MICE, INBRED C3H; MICE, INBRED C57BL; NEURAMINIDASE; SPLEEN; T-LYMPHOCYTES;

EID: 0031110967     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (40)

1. Paul, W. E. 1991. Interleukin-4: a prototypic immunoregulatory lymphokine. Blood 77:1859.
2. + T cells. Annu. Rev. Immunol. 12:635.
3. Swain, S. L. 1995. CD4 T cell development and cytokine polarization: an overview. J. Leukocyte Biol. 57:795.
4. + T cells from T cell receptor transgenic mice. J. Exp. Med. 176:1091.
5. Trinchieri, G., and F. Gerosa. 1996. Immunoregulation by IL-12. J. Leukocyte Biol. 59:505.
6. + T cells through IL-12 produced by Listeria-induced macrophages. Science 260:547.
7. + T cells to enhance priming for interferon γ production and diminishes interleukin 4 inhibition of such priming. Proc. Natl. Acad. Sci. USA 90:10188.
8. Smith, T. J., L. A. Ducharne, and J. H. Weis. 1994. Preferential expression of interleukin-12 or interleukin-4 by murine bone marrow mast cells derived in mast cell growth factor or interleukin-3. Eur. J. Immunol. 24:822.
9. + T cells promptly produce interleukin 4 in response to in vivo challenge with anti-CD3. J Exp. Med. 179:1285.
10. + T cells that promptly produce interleukin 4. Proc. Natl. Acad. Sci. USA 92:11931.
11. + cells: new clues to their origin, specificity, and function. J. Exp. Med. 182:633.
12. Daynes, R. A., T. Dowell, and B. A. Araneo. 1991. Platelet-derived growth factor is a potent biologic response modifier of T cells. J. Exp. Med. 174:1323.
13. Tara, S., and H. Nariuchi. 1988. Possible role of neuraminidase in activated T cells in the recognition of allogeneic Ia. J. Immunol. 141:440.
14. Daynes, R. A., E. Y. Enioutina, S. Butler, H. H. Mu, Z. A. McGee, and B. A. Araneo. 1996. Induction of common mucosal immunity by hormonally immunomodulated peripheral immunization. Infect. Immun. 64:1100.
15. M1 expression with increased total cellular RNA and protein content in normal thymocyte and spleen cell populations. J. Immunol. 139:2123.
16. Schumacher, J. H., A. O'Garra, B. Schrader, A. v. Kimmenade, M. W. Bond, T. R. Mossman, and R. L. Coffman. 1988. The characterization of four monoclonal antibodies specific for mouse IL-5 and development of mouse and human IL-5 enzyme-linked immunosorbent. J. Immunol. 141:1576.
17. Spencer, N. F. L., S. D. Norton, L. L. Harrison, G. Z. Li, and R. A. Daynes. 1996. Dysregulation of IL-10 production with aging: possible linkage to the age-associated decline in DHEA and its sulfated derivative. Exp. Gerontol. 31:393-408.
18. Chomczynski, P., and N. Sacchi. 1987. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:156.
19. Potier, M., L. Mameli, M. Belisle, L. Dallaire, and S. B. Melancon. 1979. Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-α-D-N-acetylneuraminate) substrate. Anal. Biochem. 94:287.
20. Mu, H.-H., and W. A. Sewell. 1993. Enhancement of interleukin-4 production by pertussis toxin. Infect. Immun. 61:2834.
21. Forsthuber, T., H. C. Yip, and P. V. Lehmann. 1996. Induction of TH1 and TH2 immunity in neonatal mice. Science 271:1728.
22. LeGros, G. G., S. S. Ben-Sasson, R. A. Seder, F. D. Finkelman, and W. E. Paul. 1990. Generation of inlerleukin 4 (IL-4)-producing cells in vivo and in vitro: IL-2 and IL-4 are required for in vitro generation of IL-4-producing cells. J. Exp. Med. 172:921.
23. Potier, M., D. L. S. Yan, and J. E. Womack. 1979. Neuraminidase deficiency in the mouse. FEBS Lett. 108:345.
24. Landolfi, N. F., J. Leone, J. E. Womack, and R. G. Cook. 1985. Activation of T lymphocyte results in an increase in H-2 encoded neuraminidase. Immunogenetics 22:159.
25. Womack, J. E., and D. L. S. Yan. 1981. Gene for neuraminidase activity on multiple hydrolases. Science 21:63.
26. Wu, G., and R. W. Leden. 1990. Stimulation of neurite outgrowth in neuroblastoma cells by neuraminidase: putative role of GM1 ganglioside in differentiation. J. Neurobiochem. 56:95.
27. Steimer, F., and J. P. Despont. 1980. Cell surface change in human normal and abnormal lymphoid cells detected by sialic acid content and sialyltransferase activity. Leuk. Res. 4:265.
28. Naraparaju, V. R., and N. Yamamoto. 1994. Roles of β-galactosidase of B lymphocytes and sialidase of T lymphocytes in inflammation-primed activation of macrophages. Immunol. Lett. 43:143.
29. 3 binding protein (group-specific component) to a macrophage activating factor by the stepwise action of β-galactosidase and sialidase of T cells. J. Immunol. 151:2794.
30. Lewis, D. B., K. S. Prickett, A. Larsen, K. Grabstein, M. Weaver, and C. B. Wilson. 1988. Restricted production of interleukin 4 by activated human T cells. Proc. Natl. Acad. Sci. USA 85:9743.
31. Swain, S. L., D. T. Mckenzie, A. D. Weinberg, and W. Hancock. 1988. Characterization of T helper 1 and 2 cell subsets in normal mice: helper T cells responsible for IL-4 and IL-5 production are present as precursors that require priming before they develop into lymphokine-secreting cells. J. Immunol. 141:3445.
32. Swain, S. L., A. D. Weinberg, M. English, and G. Houston. 1990. IL-4 directs the development of Th2-like helper effectors. J. Immunol. 145:3796.
33. + T cells into IL-4-secreting cells. J. Immunol. 152:5180.
34. Rooney, J. W., T. Hoey, and L. H. Glimcher. 1995. Coordinate and corporate roles for NF-AT and AP-1 in the regulation of the murine IL-4 gene. Immunity 2:473.
35. Weber, M. L., A. Eder, H. K. Czepa, and P. H. Krammer. 1992. T cell-specific negative regulation of transcription of the human cytokine IL-4. J. Immunol. 148:1913.
36. Fischer, T., B. Thoma, P. Scheurich, and K. Pfizenmaier. 1990. Glycosylation of the human interferon-γ receptor: N-linked carbohydrates contribute to structural heterogeneity and required for ligand binding. J. Biol. Chem. 265:1710.
37. Nagai, Y., and M. Iwamori. 1995. Cellular biology of gangliosides. In Biology of Sialic Acids. A. Rosenberg, ed. Plenum Press, New York, p. 197.
38. Bremer, E. G., S.-I. Hakomori, D. F. B. Pope, E. Raines, and R. Ross. 1984. Ganglioside-mediated modulation of cell growth, growth factor binding, and receptor phosphorylation. J. Biol. Chem. 259:6818.
39. Bremer, E. G., J. Schlessinger, and S.-I. Hakomori. 1986. Ganglioside-mediated modulation of cell growth: specific effects of GM3 on tyrosine phosphorylation of the epidermal growth factor receptor. J. Biol. Chem. 261:2434.
40. Usuki, S., S.-C. Lyu, and C. C. Sweeley. 1988. Sialidase activation of cultured human fibroblasts and the metabolism of GM3 ganglioside. J. Biol. Chem. 263: 6847.