Author
Listed:
- Lakshmi Balagopalan
(National Institutes of Health)
- Jason Yi
(National Institutes of Health)
- Tiffany Nguyen
(National Institutes of Health)
- Katherine M. McIntire
(National Institutes of Health)
- Adam S. Harned
(National Institutes of Health
Frederick National Laboratory for Cancer Research)
- Kedar Narayan
(National Institutes of Health
Frederick National Laboratory for Cancer Research)
- Lawrence E. Samelson
(National Institutes of Health)
Abstract
The relative importance of plasma membrane-localized LAT versus vesicular LAT for microcluster formation and T-cell receptor (TCR) activation is unclear. Here, we show the sequence of events in LAT microcluster formation and vesicle delivery, using lattice light sheet microscopy to image a T cell from the earliest point of activation. A kinetic lag occurs between LAT microcluster formation and vesicular pool recruitment to the synapse. Correlative 3D light and electron microscopy show an absence of vesicles at microclusters at early times, but an abundance of vesicles as activation proceeds. Using TIRF-SIM to look at the activated T-cell surface with high resolution, we capture directed vesicle movement between microclusters on microtubules. We propose a model in which cell surface LAT is recruited rapidly and phosphorylated at sites of T-cell activation, while the vesicular pool is subsequently recruited and dynamically interacts with microclusters.
Suggested Citation
Lakshmi Balagopalan & Jason Yi & Tiffany Nguyen & Katherine M. McIntire & Adam S. Harned & Kedar Narayan & Lawrence E. Samelson, 2018.
"Plasma membrane LAT activation precedes vesicular recruitment defining two phases of early T-cell activation,"
Nature Communications, Nature, vol. 9(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04419-x
DOI: 10.1038/s41467-018-04419-x
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