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Supramolecular attack particles are autonomous killing entities released from cytotoxic T cells

Abstract:
Cytotoxic T lymphocytes (CTLs) kill infected and cancerous cells. We detected transfer of cytotoxic multiprotein complexes from CTLs to target cells, termed supramolecular attack particles (SMAPs). SMAPs were rapidly released from CTLs and were autonomously cytotoxic. Mass spectrometry, immunochemical analysis and CRISPR editing identified a C-terminal fragment of thrombospondin-1 as an unexpected SMAP component that contributed to target killing. Direct stochastic optical reconstruction microscopy resolved a cytotoxic core surrounded by a thrombospondin-1 shell of ~120 nm diameter. Cryo-soft x-ray tomography analysis revealed that SMAPs had a carbon-dense shell and were stored in multicore granules. We propose that SMAPs are autonomous extracellular killing entities that deliver cytotoxic cargo based on specificity of shell components.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1126/science.aay9207

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Kennedy Institute for Rheumatology
Role:
Author
More by this author
Role:
Author
ORCID:
0000-0002-4580-2758
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Target Discovery Institute
Role:
Author
ORCID:
0000-0002-9715-5951
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Target Discovery Institute
Role:
Author
ORCID:
0000-0002-8160-2446
More by this author
Role:
Author
ORCID:
0000-0001-8091-9057


Publisher:
American Association for the Advancement of Science
Journal:
Science More from this journal
Volume:
368
Issue:
6493
Pages:
897-901
Publication date:
2020-05-07
Acceptance date:
2020-04-09
DOI:
EISSN:
1095-9203
ISSN:
0036-8075


Language:
English
Keywords:
Pubs id:
1103231
Local pid:
pubs:1103231
Deposit date:
2020-05-08
ARK identifier:

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