Zeta-chain-associated protein-70 molecule is essential for the proliferation and the final maturation of dendritic epidermal T cells

Experimental Dermatology

Volumn 14, Issue 3, 2005, Pages 188-193

  Endo, Yukie ^a   Ishikawa, Osamu ^a   Negishi, Izumi ^a  

^a GUNMA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

T cell receptor; Dendritic epidermal T cells; Syk; Zeta chain associated protein 70

Indexed keywords

CD69 ANTIGEN; CONCANAVALIN A; INTERLEUKIN 2; PROTEIN KINASE ZAP 70; T LYMPHOCYTE RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL MATURATION; CELL PROLIFERATION; CONTROLLED STUDY; DENDRITE; DENDRITIC CELL; EPIDERMIS CELL; FLOW CYTOMETRY; IMMUNOHISTOCHEMISTRY; MOUSE; NONHUMAN; PROTEIN DEFICIENCY; PROTEIN EXPRESSION; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; T LYMPHOCYTE;

ANIMALS; ANTIBODIES, MONOCLONAL; ANTIGENS, CD; ANTIGENS, CD3; ANTIGENS, DIFFERENTIATION, T-LYMPHOCYTE; CELL AGING; CELL COUNT; CELL PROLIFERATION; CELLS, CULTURED; CONCANAVALIN A; DENDRITIC CELLS; EPIDERMIS; GENE EXPRESSION; INTERLEUKIN-2; MICE; MICE, KNOCKOUT; NUCLEAR PROTEINS; PHENOTYPE; PROTEIN-TYROSINE KINASES; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; T-LYMPHOCYTES; ZAP-70 PROTEIN-TYROSINE KINASE;

EID: 15444379577     PISSN: 09066705     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0906-6705.2005.00264.x     Document Type: Article

References (31)

1. Amsen D, Kruisbeek A M. Thymocyte selection: not by TCR alone. Immunol Rev 1998: 165: 209-229.
2. Cantrell Doreen A. Transgenic analysis of thymocyte signal transduction. Nat Rev Immunol 2002: 2: 20-27.
3. Allison J P, Havran W L. The immunobiology of T cells with invariant γδ antigen receptors. Annu Rev Immunol 1991: 9: 679-705.
4. Haas W. Gamma/delta cells. Annu Rev Immunol 1993: 11: 637-685.
5. Tschachler E, Schuler G, Hutterer J, Leibl H, Wolff K, Stingl G. Expression of Thy-1 antigen by murine epidermal cells. J Invest Dermatol 1983: 81: 282-285.
6. Bergstresser P R, Tigelaar R E, Dees J H, Streilein J W. Thy-1 antigen-bearing dendritic cells populate murine epidermis. J Invest Dermatol 1983: 81: 286-288.
7. Chan A C, Iwashima M, Turck C W, Weiss A. ZAP-70: a 70 kd protein-tyrosine kinase that associates with the TCR ζ chain. Cell 1992: 71: 649-662.
8. Iwashima M, Irving B A, van-Oers N S, Chan A C, Weiss A. Sequential interactions of the TCR with two distinct cytoplasmic tyrosine kinases. Science 1994: 263: 1136-1139.
9. + thymic selection in humans lacking zap-70 kinase. Cell 1994: 76: 947-958.
10. Elder M E, Lin D, Clever J et al. Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase. Science 1994: 264: 1596-1599.
11. Chan A C, Kadlecek T A, Elder M E et al. ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency. Science 1994: 264: 1599-1601.
12. Negishi I, Motoyama N, Nakayama K et al. Essential role for ZAP-70 in both positive and negative selection of thymocytes. Nature 1995: 376: 435-438.
13. Kadlecek T A, van Oers N S C, Lefrancois L et al. Differential requirements for ZAP-70 in TCR signaling and T cell development. J Immunol 1998: 161: 4688-4694.
14. -/- mice by the Syk protein tyrosine kinase. Immunity 1997: 7: 369-377.
15. Elbe A, Foster C A, Stingl G. Isolation of T cells from mouse and human skin. In: Lefkovits I, ed. Immunology Methods Manual. San Diego: Academic Press, 1997: 1490-1501.
16. Turner M, Mee P J, Costello P S et al. Perinatal lethality and blocked B-cell development in mice lacking the tyrosine kinase Syk. Nature 1995: 378: 298-302.
17. Cheng A M, Rowley B, Pao W, Hayday A, Bolen J B, Pawson T. Syk tyrosine kinase required for mouse viability and B-cell development. Nature 1995: 378: 303-306.
18. Mallick-Wood C A, Pao W, Cheng A M et al. Disruption of epithelial γδ T cell repertoires by mutation of the Syk tyrosine kinase. Proc Natl Acad Sci USA 1996: 93: 9704-9709.
19. Leclercq G, Plum J. Stimulation of TCR Vγ3 cells by gram-negative bacteria. J Immunol 1995: 154 (10): 5313-5319.
20. Sciammas R, Kodukula P, Tang Q, Hendricks R L, Bluestone J A. T cell receptor-γ/δ cells protect mice from herpes simplex virus type 1-induced lethal encephalitis. J Exp Med 1997: 185: 1969-1975.
21. Kaminski M J, Mroczkowski T F, Krotoski W A. Dendritic epidermal γ/δ T cells (DETC) activated in vivo proliferate in vitro in response to Mycobacterium leprae antigens. Int J Dermatol 2000: 39: 603-608.
22. Kaminski M J, Cruz P D, Bergstresser P R, Takashima A. Killing of skin-derived tumor cells by mouse dendritic epidermal T-cells. Cancer Res 1993: 53: 4014-4019.
23. Schuhmachers G, Ariizumi K, Mathew P A, Bennett M, Kumar V, Takashima A. 2B4, a new member of the immunoglobulin gene superfamily, is expressed on murine dendritic epidermal T cells and plays a functional role in their killing of skin tumors. J Invest Dermatol 1995: 105: 592-596.
24. Jameson J, Ugarte K, Chen N et al. A role for skin γδ T cells in wound repair. Science 2002: 296: 747-749.
25. Jameson J M, Cauvi G, Witherden D A, Havran W L. A keratinocyte-responsive γδ TCR is necessary for dendritic epidermal T cell activation by damaged keratinocytes and maintenance in the epidermis. J Immunol 2004: 172: 3573-3579.
26. Havran W L, Chien Y H, Allison J P. Recognition of self antigens by skin-derived T cells with invariant γδ antigen receptors. Science 1991: 252: 1430-1432.
27. Boismenu R, Havran W L. Modulation of epithelial cell growth by intraepithelial γδ T cells. Science 1994: 266: 1253-1255.
28. Mallick-Wood C A, Lewis J M, Richie L I, Owen M J, Tigelaar R E, Hayday A C. Conservation of T cell receptor conformation in epidermal γδ cells with disrupted primary Vγ gene usage. Science 1998: 279: 1729-1733.
29. Hara H, Kishihara K, Matsuzaki G et al. Development of dendritic epidermal T cells with a skewed diversity of γδ TCRs in Vδ1-deficient mice. J Immunol 2000: 165: 3695-3705.
30. Itohara S, Mombaerts P, Lafaille J et al. T cell receptor δ gene mutant mice: independent generation of αβ T cells and programmed rearrangements of γδ TCR genes. Cell 1993: 72: 337-348.
31. + dendritic epidermal cells in the perinatal period. J Immunol 1989: 143: 2431-2438.