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Langerhans Cells Are Not Required for Epidermal Vgamma3 T Cell Homeostasis and Function

Overview
Journal J Leukoc Biol
Date 2011 Apr 14
PMID 21486908
Citations 4
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Abstract

This study tested the hypothesis that Vγ3 TCR-bearing T cells are influenced by LCs. Vγ3 T cells and LCs are located in the epidermis of mice. Vγ3 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 Vγ3 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 Vγ3 T cells. We show that Vγ3 T cell numbers are unaltered by LC deficiency, and Vγ3 T cells isolated from LC-deficient mice are phenotypically and upon in vitro stimulation, functionally indistinguishable from Vγ3 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 Vγ3 T cells to wounding in the absence or presence of LCs. These observations indicate that Vγ3 T cells develop and function independently of LCs.

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References
1.
Garman R, Doherty P, Raulet D . Diversity, rearrangement, and expression of murine T cell gamma genes. Cell. 1986; 45(5):733-42. DOI: 10.1016/0092-8674(86)90787-7. View

2.
Gallatin W, Weissman I, Butcher E . A cell-surface molecule involved in organ-specific homing of lymphocytes. 1983. J Immunol. 2006; 177(1):5-9. View

3.
Chorro L, Sarde A, Li M, Woollard K, Chambon P, Malissen B . Langerhans cell (LC) proliferation mediates neonatal development, homeostasis, and inflammation-associated expansion of the epidermal LC network. J Exp Med. 2009; 206(13):3089-100. PMC: 2806478. DOI: 10.1084/jem.20091586. View

4.
Zhang Y, Cado D, Asarnow D, Komori T, Alt F, Raulet D . The role of short homology repeats and TdT in generation of the invariant gamma delta antigen receptor repertoire in the fetal thymus. Immunity. 1995; 3(4):439-47. DOI: 10.1016/1074-7613(95)90173-6. View

5.
Do J, Min B . IL-15 produced and trans-presented by DCs underlies homeostatic competition between CD8 and {gamma}{delta} T cells in vivo. Blood. 2009; 113(25):6361-71. PMC: 2710929. DOI: 10.1182/blood-2008-12-192997. View