γδ T cell function varies with the expressed WC1 coreceptor

Journal of Immunology

Volumn 174, Issue 6, 2005, Pages 3386-3393

  Rogers, Aric N ^a   Vanburen, Denille G ^a   Hedblom, Emmett E ^a   Tilahun, Mulualem E ^a   Telfer, Janice C ^a   Baldwin, Cynthia L ^a  

^a UNIVERSITY OF MASSACHUSETTS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIGEN; BACTERIAL ANTIGEN; CYSTEINE; GAMMA INTERFERON; INTERLEUKIN 10; INTERLEUKIN 12; INTERLEUKIN 12 RECEPTOR BETA2; INTERLEUKIN 4; MEMBRANE PROTEIN; MESSENGER RNA; SCAVENGER RECEPTOR; T LYMPHOCYTE RECEPTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GATA 3; TRANSCRIPTION FACTOR T BET; TRANSFORMING GROWTH FACTOR BETA; UNCLASSIFIED DRUG; VC1.2 RECEPTOR; WC1 CORECEPTOR; WC1.1 RECEPTOR; DMBT1 PROTEIN, BOS TAURUS; DNA; IMMUNOGLOBULIN RECEPTOR; INTERLEUKIN 2 RECEPTOR; LYMPHOCYTE ANTIGEN RECEPTOR;

ADOLESCENT; AGING; ANIMAL CELL; ARTICLE; CATTLE; CYTOKINE PRODUCTION; EX VIVO STUDY; FEMALE; GAMMA DELTA T LYMPHOCYTE; IMMUNE RESPONSE; IMMUNOREGULATION; LYMPHOCYTE CULTURE; LYMPHOCYTE FUNCTION; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; PERIPHERAL BLOOD MONONUCLEAR CELL; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FAMILY; T LYMPHOCYTE SUBPOPULATION; TH1 CELL; AMINO ACID SEQUENCE; ANIMAL; BIOSYNTHESIS; CELL CULTURE; CELL PROLIFERATION; CHEMISTRY; CYTOLOGY; GENE EXPRESSION; GENETICS; IMMUNOLOGY; IN VITRO STUDY; METABOLISM; MOLECULAR GENETICS; SEQUENCE HOMOLOGY;

AGING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CATTLE; CELL PROLIFERATION; CELLS, CULTURED; DNA; GENE EXPRESSION; INTERFERON TYPE II; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; RECEPTORS, IMMUNOLOGIC; RECEPTORS, INTERLEUKIN-2; RNA, MESSENGER; SEQUENCE HOMOLOGY, AMINO ACID; T-LYMPHOCYTE SUBSETS;

EID: 14844339359     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.174.6.3386     Document Type: Article

References (56)

1. + γδ Tcells isolated from Babesia bovis-stimulated T cell lines. Cell. Immunol. 153:9.
2. + cells. Infect. Immun. 69:89.
3. + γδ and CD4 T cells. Infect. Immun. 70:6147.
4. Doherty, M. L., H. F. Bassett, P. J. Quinn, W. C. Davis, A. P. Kelly, and M. L. Monaghan. 1996. A sequential study of the bovine tuberculin reaction. Immunology 87:9.
5. MacHugh, N. D., J. K. Mburu, M. J. Carol, and C. R. Wyatt. 1997. Identification of two distinct subset of bovine γδ T cells with unique cell surface phenotype and tissue distribution. Immunology 92:340.
6. Hedges, J. F., D. Cockrell, L. Jackiw, N. Meissner, and M. A. Jutila. 2003. Differential mRNA expression in circulating γδ T lymphocyte subsets defines unique tissue-specific functions. J. Leukocyte Biol. 73:306.
7. Meissner, N., J. Radke, J. F. Hedges, M. White, M. Behnke, S. Bertolino, M. Abrahamsen, and M. A. Jutila. 2003. Serial analysis of gene expression in circulating γδ T cell subsets defines distinct immunoregulatory phenotypes and unexpected gene expression profiles. J. Immunol. 170:356.
8. + γδ T cells. Infect. Immun. 70:1488.
9. + γδ T cell population in cattle: a possible role in resistance to intracellular infection. Vet. Immunol. Immunopathol. 89:105.
10. Hayday, A. C. 2000. γδ cells: a right time and a right place for conserved third way of protection. Annu. Rev. Immunol. 18:975.
11. FANTOM Consortium and the RIKEN Genome Exploration Research Group Phase I & II Team. 2002. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature 420:563.
12. O'Keeffe, M. A., S. A. Metcalfe, M. D. Glew, T. Bowden, S. McInnes, W. G. Kimpton, R. N. P. Cahill, W. R. Hein, and I. D. Walker. 1994. Lymph node homing cells biologically enriched for γδ T cells express multiple genes from the T19 repertoire. Int. Immunol. 6:1687.
13. Walker, I. D., M. D. Glew, M. A. O'Keefe, S. A. Metcalfe, H. C. Clevers, P. L. J. Wijngaard, T. E. Adams, and W. R. Hein. 1994. A novel multi-gene family of sheep γδ T cells. Immunology 83:517.
14. - γδ T lymphocytes. J. Immunol. 149:3273.
15. - γδ T lymphocytes. J. Immunol. 152:3476.
16. Resnick, D., A. Pearson, and M. Krieger. 1994. The SRCR superfamily: a family reminiscent of the Ig superfamily. Trends Biochem. Sci. 19:5.
17. Baldwin, C. L., N. D. MacHugh, J. A. Ellis, J. Naessens, J. Newson, and W. I. Morrison. 1988. Monoclonal antibodies which react with bovine T-lymphocyte antigens and induce blastogenesis: tissue distribution and functional characteristics of the target antigens. Immunology 63:439.
18. Bott, C. M., J. B. Doshi, C. Morimoto, P. L. Romain, and D. A. Fox. 1993. Activation of human T cells through CD6: functional effects of a novel anti-CD6 monoclonal antibody and definition of four epitopes of the CD6 glycoprotein. Int. Immunol. 7:783.
19. Bikah, G., J. Carey, J. R. Ciallella, A. Tarakhovsky, and S. Bondada. 1996. CD5-mediated negative regulation of antigen receptor-induced growth signals in B-1 B cells. Science 274:1906.
20. Sen, G., G. Bikah, C. Venkataraman, and S. Bondada. 1999. Negative regulation of antigen receptor-mediated signaling by constitutive association of CD5 with the SHP-1 protein tyrosine phosphatase in B-1 B cells. Eur. J. Immunol. 29:3319.
21. Hanby-Flarida, M. D., O. J. Trask, T. J. Yang, and C. L. Baldwin. 1996. Modulation of WC1, a lineage-specific cell surface molecule of γδ T cells augments cellular proliferation. Immunology 88:116.
22. 1 cell cycle arrest. Eur. J. Immunol. 27:105.
23. Kanan, J. H. C., N. Nayeem, R. M. Binns, and B. M. Chain. 1997. Mechanisms for variability in a member of the scavenger-receptor cysteine-rich superfamily. Immunogenetics 46:276.
24. Goddeeris, B. M., C. L. Baldwin, O. Ole-Moiyio, and W. I. Morrision. 1986. Improved methods for purification and depletion of monocytes from bovine peripheral blood mononuclear cells: functional evaluation of monocytes in response to lectins. J. Immunol. Methods 89:165.
25. Naiman, B. M., D. Alt, C. A. Bolin, R. Zuerner, and C. L. Baldwin. 2001. Protective killed Leptospira borgpetersenii vaccine induces potent Th1 immunity comprising responses by CD4 and γδ T lymphocytes. Infect. Immun. 69:7550.
26. White, A. M., S. Blumerman, B. Naiman, and C. L. Baldwin. 2002. Expression of the bovine high affinity IL-12 receptor β2. Vet. Immunol. Immunopathol. 84:127.
27. Sathiyaseelan, T., and C. L. Baldwin. 2000. Evaluation of cell replication by bovine T cells in polyclonally-activated cultures using carboxyfluorescein succinimidyl ester (CFSE) loading and flow cytometric analysis. Res. Vet. Sci. 69:275.
28. - T cell receptor γδ T lymphocytes. Eur. J. Immunol. 20:809.
29. Taylor, B. C., J. L. Stott, R. I. Scibienski, and D. Redelman. 1992. Development and characterization of a monoclonal antibody specific for the bovine low-affinity interleukin-2 receptor, BoCD25. Immunology 77:150.
30. Weynants, V., K. C. Walravens, P. Didembourg, I. Flanagan, J. Godfroid, and J. Letesson. 1994. Quantitative assessment by flow cytometry of T-lymphocytes producing antigen-specific γ-interferon in Brucella immune cattle. Vet. Immunol. Immunopathol. 66:309.
31. Sathiyaseelan, T., A. N. Rogers, and C. L. Baldwin. 2002. Response of bovine γδ T cells to activation through CD3. Vet. Immunol. Immunopathol. 90:155.
32. Ayoub, I. A., and T. J. Yang. 1996. Age-dependent changes in peripheral blood lymphocyte subpopulations in cattle: a longitudinal study. Dev. Comp. Immunol. 20:353.
33. Baldwin, C. L., T. Sathiyaseelan, B. Naiman, A. M. White, R. Brown, S. Blumerman, A. Rogers, and S. J. Black. 2002. Activation of bovine peripheral blood γδ T cells for cell division and IFN-γ production. Vet. Immunol. Immunopathol. 87:251.
34. McDyer, J. F., Z. Li, S. John, X. Yu, C. Wu, and J. A. Ragheb. 2002. IL-2 receptor blockade inhibits late, but not early, IFN-γ and CD40 ligand expression in human T cells: disruption of both IL-12-dependent and -independent pathways of IFN-γ production. J. Immunol. 169:2736.
35. Reem, G. H., and N. H. Yeh. 1984. Interleukin 2 regulates expression of its receptor and synthesis of γ Interferon by human T lymphocytes. Science 225:429.
36. Szabo, S. J., S, T. Kim, L. Costa, X. Zhang, C. G. Fathman, and L. H. Glimcher. 2000. A novel transcription factor, T-bet, directs Th1 lineage commitment. Cell. 100:655.
37. Zheng, W., and R. A. Flavell. 1997. The transcription factor GATA-3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells. Cell 89:587.
38. Yin, Z., C. Chen, S. J. Szabo, L. H. Glimcher, A. Ray, and J. Craft. 2002. T-bet expression and failure of GATA-3 cross-regulation lead to default production of IFN-γ by γδ T cells. J. Immunol. 168:1566.
39. McGuirk, P., and K. H. G. Mills. 2002. Pathogen-specific regulatory T cells provoke a shift in the Th1/Th2 paradigm in immunity to infectious diseases. Trends Immunol. 9:450.
40. Zarrinpar, A., R. P. Bhattacharyya, and W. A. Lim. 2003. The structure and function of proline recognition domains. Science STKE 179:1-10 (Rev. RES).
41. Telfer, J. C., O. Janssen, K. V. S. Prasad, and C. E. Rudd. 1995. Src-related kinases and their receptors in T cell activation. In T Cell Receptors. J. I. Bell, M. J. Owen, and E. Simpson, eds. Oxford University Press, Oxford, pp. 164-193.
42. Mosser, D. M. 2002. The many faces of macrophage activation. J. Leukocyte Biol. 73:209.
43. Das, H., M. Sugita, and M. B. Brenner. 2004. Mechanisms of Vδ1 γδ T cell activation by microbial components. J. Immunol. 172:6578.
44. Havran, W., Y. H. Chien, J. P. Allison. 1991. Recognition of self antigens by skin-derived T cells with invariant γδ antigen receptors. Science 252:1430.
45. Szabo, S. J., A. S. Dighe, U. Gubler, and K. M. Murphy. 1997. Regulation of the interleukin (IL)-12Rβ2 subunit expression in developing T helper (Th1) and TH2 cells. J. Exp. Med. 185:817.
46. + T cells. Nat. Immunol. 3:549.
47. Hayday, A., and R. Tegelaar. 2003. Immunoregulation in the tissues by γδ T cells. Nat. Rev. Immunol. 3:233.
48. Jameson, J., D. Witherden, and W. L. Havran. 2003. T-cell effector mechanisms: γδ and CD1d-restricted subsets. Curr. Opin. Immunol. 15:349.
49. Fu, Y. X., C. E. Roark, K. Kelly, D. Drevets, P. Campbell, R. O'Brien, and W. Born. 1994. Immune protection and control of inflammatory tissue necrosis by γδ T cells. J. Immunol. 153:3101.
50. Hsieh, B., M. D. Schrenzel, T. Mulvania, H. D. Lepper, L. DiMolfetto-Landon, and D. A. Ferrick. 1996. In vivo cytokine production in murine listeriosis: evidence for immunoregulation by γδ T cells. J. Immunol. 156:232.
51. Howard, C. J., P. Sopp, K. R. Parsons, and J. Finchy. 1989. In vivo depletion of BoT4 (CD4) and of non-T4AT8 lymphocyte subsets in cattle with monoclonal antibodies. J. Immunol. 19:757.
52. Lutje, V., and S. J. Black. 1991. Cellular interactions regulating the in vitro response of bovine lymphocytes to ovalbumin. Vet. Immunol. Immunopathol. 28:275.
53. + T lymphocytes are stimulated to proliferate by autologous Theileria annulata-infected cells in the presence of interleukin-2. Scand. J. Immunol. 44:444.
54. + regulatory T cells by TGF-β induction of transcription factor Foxp3. J. Exp. Med. 198:1875.
55. Naohiro, S., Y. Tokura, M. Takigawa, and K. Egawa. 1999. Depletion of IL-10- and TGF-β-producing regulatory γδ T cells by administering a daunomycin-conjugated specific monoclonal antibody in early tumor lesions augments the activity of CTLs and NK cells. J. Immunol. 163:242.
56. Yin, Z., D. H. Zhang, T. Weite, G. Bahtiyar, S. Jung, L. Liu, X. Y. Fu, A. Ray. J. Craft. 2000. Dominance of IL-12 over IL-4 in γδ T cell differentiation leads to default production of IFN-γ: failure to down-regulate IL-12 receptor β2-chain expression. J. Immunol. 164:3056.