TNF$\beta$ Induces Cytotoxicity of Antibody-Activated CD$4^+$T-lymphocytes Against Herpes Virus-Infected Target Cells

  • Choi, Sang Hoon (Department of Marine Biomedical Science, College of Ocean Science and Technology, Kunsan National University)
  • 발행 : 2004.06.01

초록

We have extended our previous work that cross-linking CD4 molecules using specific MAb induced antigen nonspecific, MHC unrestricted killing of virally infected target cells by CD$4^+$We have extended our previous work that cross-linking CD$4^+$ molecules using specific MAb induced antigen nonspecific, MHC unrestricted killing of virally infected target cells by CD$4^+$ T cells. The killing activity of antibody activated CD$4^+$T cells was completely blocked by herbimycin A, a protein tyrosine kinase (PTK) inhibitor, but not by bisindolylamaleimide, a protein kinase C (PKC) inhibitor. Herbimycin A treated human or bovine peripheral blood CD$4^+$T cells lacked PTK activity and failed to kill virally infected target cells even after cross-linking of CD4 molecules. The CD$4^+$cross-linking failed to induce effector cell proliferation or the transcription of TNF${\beta}$ Upregulation of TNF${\beta}$ was induced by incubating the antibody activated effector cells with BHV-1 infected D17 target cells for 10 h. Anti-TNF${\beta}$ antibody partially abolished (13-44%) the direct effector cell-mediated antiviral cytotoxicity. However, this antibody neutralized 70 to 100% of antiviral activity of effector and target cell culture supernatants against BHV-1 infected D17 cells. The inhibition level of the antiviral activity by the antibody was dependent on the effector and target cell ratio. These results support the hypothesis that increased p$56^ICK enzyme activity in effector cells transduces a signal critical for effector cell recognition of viral glycoproteins expressed on the target cells. Following target cell recognition, lytic cytokines known to participate in target cell killing were produced. A better understanding of the killing activity displayed by CD$4^+$T lymphocytes following surface receptor cross-linking will provide insight into the mechanisms of cytotoxic activity directed toward virally-infected cells.T cells. The killing activity of antibody activated CD$4^+$T cells was completely blocked by herbimycin A, a protein tyrosine kinase (PTK) inhibitor, but not by bisindolylamaleimide, a protein kinase C (PKC) inhibitor. Herbimycin A treated human or bovine peripheral blood CD4T cells lacked PTK activity and failed to kill virally infected target cells even after cross-linking of CD4molecules. The CD4 cross-linking failed to induce effector cell proliferation or the transcription of TNF$\beta$. Upregulation of TNF$\beta$ was induced by incubating the antibody activated effector cells with BHV-1 infected D17 target cells for 10 h. Anti-TNF$\beta$ antibody partially abolished (13-44%) the direct effector cell-mediated antiviral cytotoxicity. However, this antibody neutralized 70 to 100% of antiviral activity of effector and target cell culture supernatants against BHV-1 infected D17 cells. The inhibition level of the antiviral activity by the antibody was dependent on the effector and target cell ratio. These results support the hypothesis that increased $56^ICK enzyme activity in effector cells transduces a signal critical for effector cell recognition of viral glycoproteins expressed on the target cells. Following target cell recognition, lytic cytokines known to participate in target cell killing were produced. A better understanding of the killing activity displayed by CD$4^+$T lymphocytes following surface receptor cross-linking will provide insight into the mechanisms of cytotoxic activity directed toward virally-infected cells.

키워드

참고문헌

  1. Abraham N, Miceli MC, Parnes JR, and Veillette A (1991) Enhancement of T-cell responsiveness by the Iymphocyte-specific tyrosine protein kinase $p56^{lck}$/. Nature 350: 62-64 https://doi.org/10.1038/350062a0
  2. Bernard M, Spriewald J, Billing S, Ensminger SM, Morris PJ, and Wood KJ (2002) Linked unresponsiveness: early cytokine gene expression profiles in cardiac allografts following pretreatment of recipients with bone marrow cells expressing conor MHC alloantigen. Cytokine 19: 6-13 https://doi.org/10.1006/cyto.2002.1041
  3. Biddison WE, Rao PE, Talle MA, Goldstein G, and Shaw S (1982) Possible involvement of the OKT4 molecule in T cell recognition of class II HLA antigens. J Exp Med 156: 1065-1076 https://doi.org/10.1084/jem.156.4.1065
  4. Carrel S, Salvi S, Gallay P, Rapin C, and Sekaly RP (1991) Positive signal transduction via surface CD4 molecules does not need coexpression of the CD3/TcR complex. Res Immunol 142: 97-102 https://doi.org/10.1016/0923-2494(91)90017-D
  5. Choi SH and Splitter GA (1994) Induction of MHC-unrestricted cytolytic $CD4^+$ T cells against virally infected target cells by cross-linking CD4 molecules. J Immunol 153: 3874-3881
  6. Eiseman E and Bolen JB (1990) Src-related tyrosine protein kinases as signaling components in hematopoietic cells. Cancer Cells 2: 303-308
  7. Fragoso R, Ren D, Zhang X, Su MWC, Burakoff SJ, and Jin YJ (2003) Lipid raft distribution of CD4 depends on its palmitoylation and association with Lck, and evidence for CD4-induced lipid raft aggregation as an additional mechanism to enhance CD3 signaling. J Immunol 170: 913-921 https://doi.org/10.4049/jimmunol.170.2.913
  8. Glaichenhaus N, Shastri N, Littman DR, and Turner JM (1991) Requirement for association of $p56^{lck}$ CD4 in antigen specific signal transuction in T cells. Cell 64: 511-520 https://doi.org/10.1016/0092-8674(91)90235-Q
  9. Go C, Lanky DW, Fitch FW, and Miller J (1993) Anergized T cell clones retain their cytolytic ability. J Immunol 150: 367-376
  10. Golding H, Munitz TI, and Singer A (1985) Characterization of antigen-specific, la-restricted, $L3T4^+$ cytolytic T lymphocytes and assessment of thymic influence on their self specificity. J Exp Med 162: 943-961 https://doi.org/10.1084/jem.162.3.943
  11. Gratton S, Haughn L, Sekaly RP, and Julius M (2000) The extracellular domain of CD4 regulates the initiation of T cell activation. Mol Immunol 37: 213-219 https://doi.org/10.1016/S0161-5890(00)00046-8
  12. Henkart PA (1985) Mechanism of lymphocyte-mediated cytotoxicity. Annu Rev Immunol 3: 31-58 https://doi.org/10.1146/annurev.iy.03.040185.000335
  13. Hivroz C, Mazerolles F, Soula M, Fagard R, Graton S, Meloche S, Sekaly RP, and Fischer A (1993) Human immunodeficiency virus gp120 and derived peptides activate protein tyrosine kinase $p56^{lck}$ in human $CD4^+$T lymphocytes. Eur J Immunol 23: 600-605 https://doi.org/10.1002/eji.1830230303
  14. Horak ID, Popovic M, Horak EM, Lucas PJ, Gress RE, June CH, and Bolen JB (1990) No T-cell tyrosine protein kinase signalling or calcium mobilization after CD4 association with HIV-1 or HIV-1 gp120. Nature 348: 557-560 https://doi.org/10.1038/348557a0
  15. June CH, Fletcher MC, Ledbetter JA, and Samelson LE (1990) Increase in tyrosine phosphorylation are detectable before phospholipase C activation after T cell receptor stimulation. J Immunol 144: 1591-1599
  16. Ju S-T, Ruddle NH, Strack PI, Dorf ME, and Dekruyff RH (1990) Expression of two distinct cytolytic mechanisms among murine CD4 subsets. J Immunol 144: 23-31
  17. Juszczak RJ, Turchin H, Trun A, Cuhp H, and Kassis S (1991) Effect of human immunodeficiency virus gp120 glycoprotein on the association of the protein tyrosine kinase $p56^{lck}$ with CD4 in human T lymphocytes. J Biol Chem 266: 11176-11181
  18. Kamitz L, Sutor SL, Torigol T, Reed JC, Bell MP, McKean DJ, Leibson PJ, and Abraham RT (1992) Effects of $p56^{lck}$ deficiency on the growth and cytolytic effector function of an interleukin-2-dependent cytotoxic T-cell line. Mol Cell Biol 12: 4521-4530 https://doi.org/10.1128/MCB.12.10.4521
  19. Klausner RD and Samelson LE (1991) T cell antigen receptor activation pathways: the tyrosine kinase connection. Cell 64: 875-878 https://doi.org/10.1016/0092-8674(91)90310-U
  20. Leeuwenberg JFM, Spits H, Tax WJM, and Capel PJA (1985) Induction of nonspecific cytotoxicity by monoclonal anti-T3 antibodies. J Immunol 134: 3770-3775
  21. Liu C-C, Rafii S, Granelli-Piperno A, Trapani JA, and Young JDE (1989) Perforin and serine esterase gene expression in stimulated human T cells: kinetics, mitogen requirements, and effects of cyclosporin A. J Exp Med 170: 2105-2118 https://doi.org/10.1084/jem.170.6.2105
  22. Luo K and Sefton BM (1990) Cross-linking of T-cell surface molecules CD4 and CD8 stimulates phosphorylation of the lck tyrosine protein kinase at the autophosphorylation site. Mol Cell Biol 10: 5305-5309 https://doi.org/10.1128/MCB.10.10.5305
  23. Maddon PJ, Dalgleish AG, McDougal SJ, Glapham PR, Weiss RA, and Axel R (1986) The T4 gene encodes the AIDS virus receptor and is expressed in the immune system and the brain. Cell 47: 333-348 https://doi.org/10.1016/0092-8674(86)90590-8
  24. Molina TJ, Bachmann MF, Kundig TM, Zinkernagel RM, and Mak TW (1993) Peripheral T cells in mice lacking $p56^{lck}$ do not express significant antiviral effector functions. J Immunol 151: 699-706
  25. Nakamura M, Ross DT, Briner TJ, and Gefter ML (1986) Cytolytic activity of antigen-specific T cells with helper phenotype. J Immunol 136: 44-47
  26. O'Shea JJ, Weissman AM, Kennedy ICS, and Ortalo FR (1991) Engagement of the natural killer cell IgG Fc receptor results in tyrosine phosphorylation of the ${\zeta}$ chain. Proc Natl Acad Sci USA 88: 350-354 https://doi.org/10.1073/pnas.88.2.350
  27. Salcedo TW, Kurosaki T, Kanakaraj P, Ravetch JV, and Perussia B (1993) Physical and functional association of $p56^{lck}$ with $Fc{\gamma}Rllla$ (CD16) in NK cells. J Exp Med 177: 1475-1480 https://doi.org/10.1084/jem.177.5.1475
  28. Samelson LE, Phillips AF, Luong ET, and Klausner RD (1990) Association of the fyn protein-tyrosine kinase with the T cell antigen receptor. Proc Natl Acad Sci USA 87: 4358-4362 https://doi.org/10.1073/pnas.87.11.4358
  29. Schwab R, Crow MK, Russo C, and Weksler ME (1985) Requirements of T cell activation by OKT3 monoclonal antibody: role of modulation of T3 molecules and interleukin 1. J Immunol 135: 1714-1718
  30. Strack P, Martin C, Satio S, Dekruyff RH, and Ju S-T (1990) Metabolic inhibitors distinguish cytolytic activity of CD4 and CD8 clones. Eur J Immunol 20: 179-184 https://doi.org/10.1002/eji.1830200126
  31. Sugie K, Kawakami T, Maeda Y, Kawabe T, Uchida A, and Yodoi J (1991) Fyn tyrosine kinase associated with $Fc{\varepsilon}RII/CD23.$ Possible multiple roles in lymphocyte activation. Proc Natl Acad Sci USA 88: 9132-9135 https://doi.org/10.1073/pnas.88.20.9132
  32. Ting AT, Einspahr KJ, Abraham RT, and Leibson PJ (1991) $Fc{\gamma}$ receptor signal transduction in natural killer cells: coupling to phospholipase C via a G protein-independent, but tyrosine kinase dependent pathway. J Immunol 147: 3122-3127
  33. Ting CC and Hargrove ME (1991) Anti-CD3 antibody-induced activated killer cells: cytokines as the additional signals for activation of killer cells in effector phase to mediated slow lysis. Cell Immunol 135: 273-284 https://doi.org/10.1016/0008-8749(91)90273-E
  34. Tite JP (1990) Differential requirement for protein synthesis and cytolysis mediated by class I and class II MHC-restricted cytotoxic T cells. Immunology 70: 440-445
  35. Tite JP and Janeway CA (1984) Cloned helper T cells can kill B lymphoma cells in the presence of specific antigen: la restriction and cognate vs no cognate interaction in cytolysis. Eur J Immunol 14: 878-886 https://doi.org/10.1002/eji.1830141004
  36. Tite JP, Powell MB, and Ruddle NH (1985) Protein-antigen specific la-restricted cytolytic T cell: analysis of frequency, target cell susceptibility, and mechanism of cytolysis. J Immunol 135: 25-33
  37. Uehara Y, Fukazawa H, Murakami Y, and Mizuno S (1989) Irreversible inhibition of v-src tyrosine kinase activity by herbimycin A and its abrogation by sulfhydryl compounds. Biochem Biophys Res Commun 163: 803-808 https://doi.org/10.1016/0006-291X(89)92293-6
  38. Veillette A, Bookman MA, Horak EM, Samelson LE, and Bolen JB (1989) Signal transduction through the CD4 receptor involves the activation of the internal membrane tyrosine-protein kinase $p56^{lck}$. Nature 338: 257-259 https://doi.org/10.1038/338257a0
  39. Veillette A, Bookman MA, Horak EM, and Bolen JB (1988) The CD4 and CD8 T cell surface antigens are associated with the internal membrane tyrosine-protein kinase $p56^{lck}.$ Cell 55: 301-308 https://doi.org/10.1016/0092-8674(88)90053-0
  40. Vivier E, Morin P, O'Brien C, Druker B, Schlossman SF, and Anderson P (1991) Tyrosine phosphorylation of the $Fc{\gamma}Rlll$ (CD16): ${\zeta}$ complex in human natural killer cells. Induction by antibody-dependent cytotoxicity bur not by natural killing. J Immunol 146: 206-210
  41. Weiss A, Imboden J, Hardy K, Manger B, Terhorst C, and Stobo T (1986) The role of the T3/antigen receptor complex in T-cell activation. Annu Rev Immunol 4: 593-619 https://doi.org/10.1146/annurev.iy.04.040186.003113
  42. Wong GHW and Goeddel (1986) Tumor necrosis factor ${\alpha}\;and\;{\beta}$ inhibit virus replication and synergize with interferons. Nature 323: 819-822 https://doi.org/10.1038/323819a0
  43. Wong GHW, Krowka JF, Stites DP, and Goeddel DV (1988) In vitro anti-human immunodeficiency virus activities of tumor necrosis factor ${\alpha}$ and $interferon-{\gamma}$. J Immunol 140: 120-124
  44. Young JD and Cohn ZA (1986) Role of granule proteins in lymphocyte-mediated killing. J Cell Biochem 32: 1510-1156 https://doi.org/10.1002/jcb.240320207