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 Immunoljournal_title
Nature immunologyauthors
Beemiller P,Jacobelli J,Krummel MFdoi
10.1038/ni.2364subject
Has Abstractpub_date
2012-07-01 00:00:00pages
787-95issue
8eissn
1529-2908issn
1529-2916pii
ni.2364journal_volume
13pub_type
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abstract:: ...
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