F-actin-binding protein drebrin regulates CXCR4 recruitment to the immune synapse.

Abstract:

:The adaptive immune response depends on the interaction of T cells and antigen-presenting cells at the immune synapse. Formation of the immune synapse and the subsequent T-cell activation are highly dependent on the actin cytoskeleton. In this work, we describe that T cells express drebrin, a neuronal actin-binding protein. Drebrin colocalizes with the chemokine receptor CXCR4 and F-actin at the peripheral supramolecular activation cluster in the immune synapse. Drebrin interacts with the cytoplasmic tail of CXCR4 and both proteins redistribute to the immune synapse with similar kinetics. Drebrin knockdown in T cells impairs the redistribution of CXCR4 and inhibits actin polymerization at the immune synapse as well as IL-2 production. Our data indicate that drebrin exerts an unexpected and relevant functional role in T cells during the generation of the immune response.

journal_name

J Cell Sci

journal_title

Journal of cell science

authors

Pérez-Martínez M,Gordón-Alonso M,Cabrero JR,Barrero-Villar M,Rey M,Mittelbrunn M,Lamana A,Morlino G,Calabia C,Yamazaki H,Shirao T,Vázquez J,González-Amaro R,Veiga E,Sánchez-Madrid F

doi

10.1242/jcs.064238

subject

Has Abstract

pub_date

2010-04-01 00:00:00

pages

1160-70

issue

Pt 7

eissn

0021-9533

issn

1477-9137

pii

jcs.064238

journal_volume

123

pub_type

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