Integration of the movement of signaling microclusters with cellular motility in immunological synapses.

Abstract:

:Immune synapses form between T cells and antigen-presenting cells (APCs). Increasing evidence suggests synapses must form flexibly to accommodate ongoing motility and displacement of the synapse. Here, time-lapse total internal reflection fluorescence (TIRF) microscopy showed that signaling via the T cell antigen receptor (TCR) occurred during synapse translation. TCR microclusters in motile synapses did not flow directly into supramolecular activating complexes (SMACs) but were directed, independently of myosin II contractility, toward an F-actin-poor 'sink' region. Inward microcluster flow often followed collapse of the leading edge, which suggested that actin depolymerization regulated microcluster flow and the formation of SMACs. The coordination of TCR movement with the translocation of this 'sink' shows how T cells coordinate TCR signaling and microcluster flow in dynamic physiological synapses.

journal_name

Nat Immunol

journal_title

Nature immunology

authors

Beemiller P,Jacobelli J,Krummel MF

doi

10.1038/ni.2364

subject

Has Abstract

pub_date

2012-07-01 00:00:00

pages

787-95

issue

8

eissn

1529-2908

issn

1529-2916

pii

ni.2364

journal_volume

13

pub_type

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