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Cutting edge: identification of E-cadherin as a ligand for the murine killer cell lectin-like receptor G1.

Authors :
Gründemann C
Bauer M
Schweier O
von Oppen N
Lässing U
Saudan P
Becker KF
Karp K
Hanke T
Bachmann MF
Pircher H
Source :
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2006 Feb 01; Vol. 176 (3), pp. 1311-5.
Publication Year :
2006

Abstract

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.

Details

Language :
English
ISSN :
0022-1767
Volume :
176
Issue :
3
Database :
MEDLINE
Journal :
Journal of immunology (Baltimore, Md. : 1950)
Publication Type :
Academic Journal
Accession number :
16424155
Full Text :
https://doi.org/10.4049/jimmunol.176.3.1311