Germ-line and rearranged Tcrd transcription distinguish bona fide NK cells and NK-like γδ T cells

被引:67
作者
Stewart, Charles A.
Walzer, Thierry
Robbins, Scott H.
Malissen, Bernard
Vivier, Eric
Prinz, Immo
机构
[1] Med Hannover Hannover, Inst Immunol, D-30625 Hannover, Germany
[2] Univ Mediterranee, Ctr Immunol, Marseille, France
[3] INSERM, U 631, Marseille, France
[4] CNRS, UMR 6102, Marseille, France
[5] Hop Conception, Serv Immunol, Marseille, France
关键词
gamma delta T cells; NK cells; TCR rearrangement; thymic development;
D O I
10.1002/eji.200737354
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NK cells and gamma delta T cells are distinct subsets of lymphocytes that contextually share multiple phenotypic and functional characteristics. However, the acquisition and the extent of these similarities remain poorly understood. Here, using T cell receptor 6 locus-histone 2B-enhanced GFP (Tcrd-H2BEGFP) reporter mice, we show that germline transcription of Tcrd occurs in all maturing NK cells. We also describe a population of mouse NK-like cells that are indistinguishable from "bona fide" NK cells using standard protocols. Requirements for V(D)J recombination and a functional thymus, along with very low-level expression of surface TCR76 but high intracellular CD3, define these cells as gamma delta T cells. "NK-like gamma delta T cells" are CD127(+), have a memory-activated phenotype, express multiple NK cell receptors and readily produce interferon-gamma in response to IL-12/IL-18 stimulation. The close phenotypic resemblance between NK cells and NK-like 78 T cells is a source of experimental ambiguity in studies bridging NK and T cell biology, such as those on thymic NK cell development. Instead, it ascribes chronic TCR gamma delta engagement as a means of acquiring NK-like function.
引用
收藏
页码:1442 / 1452
页数:11
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