Signal strength controls the rate of polarization within CTLs during killing.

Abstract:

:Cytotoxic T lymphocytes (CTLs) are key effector cells in the immune response against viruses and cancers, killing targets with high precision. Target cell recognition by CTL triggers rapid polarization of intracellular organelles toward the synapse formed with the target cell, delivering cytolytic granules to the immune synapse. Single amino acid changes within peptides binding MHC class I (pMHCs) are sufficient to modulate the degree of killing, but exactly how this impacts the choreography of centrosome polarization and granule delivery to the target cell remains poorly characterized. Here we use 4D imaging and find that the pathways orchestrating killing within CTL are conserved irrespective of the signal strength. However, the rate of initiation along these pathways varies with signal strength. We find that increased strength of signal leads to an increased proportion of CTLs with prolonged dwell times, initial Ca2+ fluxes, centrosome docking, and granule polarization. Hence, TCR signal strength modulates the rate but not organization of effector CTL responses.

journal_name

J Cell Biol

authors

Frazer GL,Gawden-Bone CM,Dieckmann NMG,Asano Y,Griffiths GM

doi

10.1083/jcb.202104093

subject

Has Abstract

pub_date

2021-10-04 00:00:00

issue

10

eissn

0021-9525

issn

1540-8140

pii

212498

journal_volume

220

pub_type

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