Langerhans cells are not required for epidermal Vγ3 T cell homeostasis and function

被引:6
作者
Taveirne, Sylvie [1 ]
De Colvenaer, Veerle [1 ]
Van Den Broeck, Tina [1 ]
Van Ammel, Els [1 ]
Bennett, Clare L. [2 ]
Taghon, Tom [1 ]
Vandekerckhove, Bart [1 ]
Plum, Jean [1 ]
Clausen, Bjorn E. [3 ]
Kaplan, Daniel H. [4 ]
Leclercq, Georges [1 ]
机构
[1] Univ Ghent, Dept Clin Chem Microbiol & Immunol, B-9000 Ghent, Belgium
[2] UCL, Dept Haematol, London, England
[3] Univ Med Ctr, Erasmus MC, Dept Immunol, Rotterdam, Netherlands
[4] Univ Minnesota, Dept Dermatol, Ctr Immunol, Minneapolis, MN 55455 USA
关键词
skin; Langerin DTA mice; Langerin DTR mice; LC deficiency; NATURAL-KILLER-CELLS; DENDRITIC CELLS; CONTACT HYPERSENSITIVITY; DEFICIENT MICE; BONE-MARROW; GAMMA-GENES; IN-VITRO; RECEPTOR; SKIN; EXPRESSION;
D O I
10.1189/jlb.1010581
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study tested the hypothesis that V gamma 3 TCR-bearing T cells are influenced by LCs. V gamma 3 T cells and LCs are located in the epidermis of mice. V gamma 3 T cells represent the main T cell population in the skin epithelium and play a crucial role in maintaining the skin integrity, whereas LCs are professional APCs. Although V gamma 3 T cells and LCs form an interdigitating network in the epidermis, not much is known about their reciprocal influence and/or interdependence. We used two different LC-deficient mouse models, in which LCs are constitutively or inducibly depleted, to investigate the role of LCs in maturation, homeostasis, and function of V gamma 3 T cells. We show that V gamma 3 T cell numbers are unaltered by LC deficiency, and V gamma 3 T cells isolated from LC-deficient mice are phenotypically and upon in vitro stimulation, functionally indistinguishable from V gamma 3 T cells isolated from WT mice based on their cytotoxic potential and cytokine production. Additionally, in vivo skin-wounding experiments show no major difference in response of V gamma 3 T cells to wounding in the absence or presence of LCs. These observations indicate that V gamma 3 T cells develop and function independently of LCs. J. Leukoc. Biol. 90: 61-68; 2011.
引用
收藏
页码:61 / 68
页数:8
相关论文
共 41 条
[11]   Skin and Peripheral Lymph Node Invariant NKT Cells Are Mainly Retinoic Acid Receptor-Related Orphan Receptor γt+ and Respond Preferentially under Inflammatory Conditions [J].
Doisne, Jean-Marc ;
Becourt, Chantal ;
Amniai, Latiffa ;
Duarte, Nadia ;
Le Luduec, Jean-Benoit ;
Eberl, Gerard ;
Benlagha, Kamel .
JOURNAL OF IMMUNOLOGY, 2009, 183 (03) :2142-2149
[12]  
Fraser KP, 2002, EUR J IMMUNOL, V32, P868, DOI 10.1002/1521-4141(200203)32:3<868::AID-IMMU868>3.0.CO
[13]  
2-A
[14]   MOUSE EPIDERMAL IA MOLECULES HAVE A BONE-MARROW ORIGIN [J].
FRELINGER, JG ;
HOOD, L ;
HILL, S ;
FRELINGER, JA .
NATURE, 1979, 282 (5736) :321-323
[15]  
Gallatin WM, 2006, J IMMUNOL, V177, P5
[16]   DIVERSITY, REARRANGEMENT, AND EXPRESSION OF MURINE T-CELL GAMMA-GENES [J].
GARMAN, RD ;
DOHERTY, PJ ;
RAULET, DH .
CELL, 1986, 45 (05) :733-742
[17]   Resident skin-specific γδ T cells provide local, nonredundant regulation of cutaneous inflammation [J].
Girardi, M ;
Lewis, J ;
Glusac, E ;
Filler, RB ;
Geng, LP ;
Hayday, AC ;
Tigelaar, RE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (07) :855-867
[18]   Regulation of cutaneous malignancy by γδ T cells [J].
Girardi, M ;
Oppenheim, DE ;
Steele, CR ;
Lewis, JM ;
Glusac, E ;
Filler, R ;
Hobby, P ;
Sutton, B ;
Tigelaar, RE ;
Hayday, AC .
SCIENCE, 2001, 294 (5542) :605-609
[19]   LIMITED DIVERSITY OF T-CELL RECEPTOR GAMMA-CHAIN EXPRESSION OF MURINE THY-1+ DENDRITIC EPIDERMAL-CELLS REVEALED BY V-GAMMA-3-SPECIFIC MONOCLONAL-ANTIBODY [J].
HAVRAN, WL ;
GRELL, S ;
DUWE, G ;
KIMURA, J ;
WILSON, A ;
KRUISBEEK, AM ;
OBRIEN, RL ;
BORN, W ;
TIGELAAR, RE ;
ALLISON, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) :4185-4189
[20]   RECOGNITION OF SELF ANTIGENS BY SKIN-DERIVED T-CELLS WITH INVARIANT GAMMA-DELTA-ANTIGEN RECEPTORS [J].
HAVRAN, WL ;
CHIEN, YH ;
ALLISON, JP .
SCIENCE, 1991, 252 (5011) :1430-1432