Interaction of KLRG1 with E-cadherin: new functional and structural insights.

Abstract:

:The killer cell lectin-like receptor G1 (KLRG1) is an inhibitory receptor expressed by memory T cells and NK cells in man and mice. It is frequently used as a cell differentiation marker and members of the cadherin family are ligands for KLRG1. The present study provides new insights into the interaction of mouse KLRG1 with E-cadherin. Firstly, we demonstrate that co-engagement of KLRG1 and CD3/TCR in a spatially linked manner was required for inhibition arguing against the notion that KLRG1-ligation per se transmits inhibitory signals. Secondly, experiments with T cells carrying Y(7)F-mutant KLRG1 molecules with a replacement of the tyrosine residue to phenylalanine in the single ITIM indicated that the inhibitory activity of KLRG1 is counteracted to some degree by increased interaction of KLRG1(+) T cells with E-cadherin expressing target cells. Thirdly, we demonstrate that deletion of the first or the second external domain of E-cadherin abolished reactivity in KLRG1-reporter cell assays. Finally, we made the intriguing observation that KLRG1 formed multimeric protein complexes in T cells in addition to the previously described mono- and dimeric molecules.

journal_name

Eur J Immunol

authors

Rosshart S,Hofmann M,Schweier O,Pfaff AK,Yoshimoto K,Takeuchi T,Molnar E,Schamel WW,Pircher H

doi

10.1002/eji.200838690

subject

Has Abstract

pub_date

2008-12-01 00:00:00

pages

3354-64

issue

12

eissn

0014-2980

issn

1521-4141

journal_volume

38

pub_type

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