Clustering of the ζ-Chain Can Initiate T Cell Receptor Signaling.

Int J Mol Sci

EMBL Australia Node in Single Molecule Science, School of Medical Sciences, The University of New South Wales, Sydney 2052, Australia.

Published: May 2020

AI Article Synopsis

  • T cell activation starts with the binding of a ligand to the T cell receptor (TCR), which triggers intracellular phosphorylation in the TCR-CD3 complex.
  • Researchers developed an optogenetic tool that controls the clustering of the ζ-chain, demonstrating that this clustering alone can initiate T cell activation processes, including various phosphorylation events and calcium flux.
  • The study found that in COS-7 cells, only the presence of Lck was needed for ζ-chain phosphorylation when clustering occurs, highlighting the importance of receptor clustering in TCR signaling.

Article Abstract

T cell activation is initiated when ligand binding to the T cell receptor (TCR) triggers intracellular phosphorylation of the TCR-CD3 complex. However, it remains unknown how biophysical properties of TCR engagement result in biochemical phosphorylation events. Here, we constructed an optogenetic tool that induces spatial clustering of ζ-chain in a light controlled manner. We showed that spatial clustering of the ζ-chain intracellular tail alone was sufficient to initialize T cell triggering including phosphorylation of ζ-chain, Zap70, PLCγ, ERK and initiated Ca flux. In reconstituted COS-7 cells, only Lck expression was required to initiate ζ-chain phosphorylation upon ζ-chain clustering, which leads to the recruitment of tandem SH2 domain of Zap70 from cell cytosol to the newly formed ζ-chain clusters at the plasma membrane. Taken together, our data demonstrated the biophysical relevance of receptor clustering in TCR signaling.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279048PMC
http://dx.doi.org/10.3390/ijms21103498DOI Listing

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