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Cutting Edge: Identification of E-Cadherin as a Ligand for the Murine Killer Cell Lectin-Like Receptor G1
Author(s) -
Carsten Gründemann,
Monika Bauer,
Oliver Schweier,
Nanette von Oppen,
Ute Lässing,
Philippe Saudan,
KarlFriedrich Becker,
Klaus Karp,
Thomas Hanke,
Martin F. Bachmann,
Hanspeter Pircher
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.3.1311
Subject(s) - interleukin 21 , cytotoxic t cell , il 2 receptor , interleukin 12 , lymphokine activated killer cell , microbiology and biotechnology , zap70 , cd49b , biology , natural killer t cell , cd8 , antigen presenting cell , t cell , janus kinase 3 , immunology , immune system , in vitro , biochemistry
The killer cell lectin-like receptor G1 (KLRG1) is expressed by NK cells and by T cells. In both humans and mice, KLRG1 identifies Ag-experienced T cells that are impaired in their proliferative capacity but are capable of performing effector functions. In this study, we identified E-cadherin as a ligand for murine KLRG1 by using fluorescently labeled, soluble tetrameric complexes of the extracellular domain of the murine KLRG1 molecule as staining reagents in expression cloning. Ectopic expression of E-cadherin in B16.BL6 target cells did not affect cell-mediated lysis by lymphokine-activated NK cells and by CD8 T cells but inhibited Ag-induced proliferation and induction of cytolytic activity of CD8 T cells. E-cadherin is expressed by normal epithelial cells, Langerhans cells, and keratinocytes and is usually down-regulated on metastatic cancer cells. KLRG1 ligation by E-cadherin in healthy tissue may thus exert an inhibitory effect on primed T cells.

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