Carnegie Mellon University
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Fluorescence Microscope movies of cytotoxic T cells interacting with tumor cells

dataset
posted on 2020-07-21, 18:45 authored by Rachel Ambler, Grace Edmunds, sin lih tan, Silvia Cirillo, Jorge Huele Carrasco, Xiongtao RuanXiongtao Ruan, Robert MurphyRobert Murphy, Christoph Wülfing
<p>CD8+ T cell killing of tumor cells is suppressed by the tumor microenvironment. Inhibitory receptors, prominently PD-1, are key mediators of this suppression. To discover cellular defects triggered by tumor exposure and associated PD-1 signaling, we have established an ex vivo imaging approach to investigate CD8+ tumor infiltrating lymphocytes (TILs) interacting with tumor targets. Whilst TIL:tumor cell couples still formed, couple stability deteriorated within 1-2 minutes. This was</p> <p>associated with impaired F-actin clearing from the center of the cellular interface, reduced calcium signaling, increased TIL locomotion and impaired tumor cell killing. Interaction of CD8+ lymphocytes with tumor cell spheroids in vitro induced a similar phenotype, supporting a critical role of direct T cell tumor cell contact. Diminished engagement of PD-1 within the tumor, but not acute ex vivo blockade, partially restored cell couple maintenance and killing. PD-1 thus suppresses TIL function by inducing a polarization-impaired state.</p>

Funding

Wellcome Trust 102387/Z/13/Z

Wellcome Trust 201254/Z/16/Z

U.K. BBSRC BB/P011578/1 – 15 NFSBIO

ERC PCIG11-GA-2012-321554

U.S. National Science Foundation MCB1616492

U.S. National Institutes of Health P41 GM103712

History

Date

2020-03-17