Macrophages express multiple ligands for γδ TCRs

被引:21
作者
Aydintug, M. Kemal [1 ,2 ]
Roark, Christina L. [1 ,2 ]
Chain, Jennifer L. [1 ,2 ]
Born, Willi K. [1 ,2 ]
O'Brien, Rebecca L. [1 ,2 ]
机构
[1] Natl Jewish Med & Res Ctr, Integrated Dept Immunol, Denver, CO 80206 USA
[2] Univ Colorado, Denver, CO 80262 USA
关键词
rodent; T cells; cell surface molecules; T cell receptors;
D O I
10.1016/j.molimm.2008.02.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As only a handful of ligands have been identified, the general nature of the ligands recognized by gamma delta T cells remains unresolved. In this study, soluble multimerized gamma delta T cell receptors (smTCRs) representing the TCRs of two gamma delta T cell subsets common in the mouse were used to detect and track their own ligands. Ligands for both subsets were found on resident peritoneal macrophages taken from untreated mice, and the expression of both was further induced by Listeria monocytogenes infection. Nevertheless, the two types of ligand differ from one another in abundance, in the kinetics of their induction following Listeria infection, and in their ability to be induced by in vitro culture with lipopolysaccharide (LPS). Surprisingly, because both are detectable on normal macrophages, these host-derived ligands are likely expressed constitutively, but are induced to higher levels of expression by stress or inflammation. In contrast to T22 and other known cell surface ligands for gamma delta T cells in mice and humans, expression of these smTCR-defined ligands does not depend on beta 2-microglobulin, suggesting that they are not MHC class I or class I-like molecules. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3253 / 3263
页数:11
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