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Persistent Identifier
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perma:LIST.YUVM65 |
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Publication Date
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2026-07-06 |
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Title
| Cancer cells suppress NK cell activity by actin-driven polarization of inhibitory ligands to the immunological synapse [* Cross-Reference *] |
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Other Identifier
| https://doi.org/10.1073/pnas.2503259122
OpenAlex ID: https://openalex.org/W4412990231 |
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Author
| Céline Hoffmann (Luxembourg Institute of Health, Cytoskeleton (United States)) - ORCID: https://orcid.org/0000-0002-7564-2329
Liza Filali (Luxembourg Institute of Health, Cytoskeleton (United States)) - ORCID: https://orcid.org/0000-0003-0985-4136
Hannah Wurzer (University of Luxembourg, Luxembourg Institute of Health, Luxembourg Institute of Science and Technology, Cytoskeleton (United States)) - ORCID: https://orcid.org/0000-0001-5816-1286
Diogo Pereira Fernandes (University of Luxembourg, Luxembourg Institute of Health, Luxembourg Institute of Science and Technology, Cytoskeleton (United States)) - ORCID: https://orcid.org/0009-0006-3599-246X
Takouhie Mgrditchian (Luxembourg Institute of Health, Cytoskeleton (United States))
Wanxin Huang (University of Luxembourg, Luxembourg Institute of Health, Luxembourg Institute of Science and Technology, Cytoskeleton (United States))
Flora Moreau (Luxembourg Institute of Health, Cytoskeleton (United States))
Max Krecké (University of Luxembourg, Luxembourg Institute of Health, Luxembourg Institute of Science and Technology, Cytoskeleton (United States)) - ORCID: https://orcid.org/0000-0001-7158-9033
Clément Thomas (Luxembourg Institute of Health, Cytoskeleton (United States)) - ORCID: https://orcid.org/0000-0001-6720-5615 |
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Point of Contact
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LIST QDKM (LIST) |
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Description
| Natural killer (NK) cells engage target cells via the immunological synapse (IS), where inhibitory and activating signals determine whether NK cell cytotoxicity is suppressed or activated. We previously reported that cancer cells can rapidly remodel their actin cytoskeleton upon NK cell engagement, leading to F-actin accumulation at the synapse. Here, we show that this process inhibits NK cell activation as indicated by impaired MTOC and lytic granule polarization. Exploring the underlying mechanism, we demonstrate that actin remodeling drives the recruitment of inhibitory ligands, such as HLA-A, -B, and -C, to the synapse. Disrupting HLA interaction with their cognate inhibitory receptors KIRs restores NK cell activation. Using NK cells expressing inhibitory KIR receptors, matched or unmatched to HLA molecules on cancer cells, we show that synaptic F-actin accumulation and matching KIR–HLA interactions jointly suppress NK cell cytotoxicity. Our findings reveal an immune evasion strategy in which cancer cells impair NK cell activation by altering synaptic signaling through actin cytoskeleton–driven recruitment of inhibitory signals to the IS. (2025-08-05)
***This entry has been automatically imported via OpenAlex by LIST harvest scripts. Please refer to https://doi.org/10.1073/pnas.2503259122 for the original and latest version of the publication*** (2026-07-01) |
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Subject
| Medicine, Health and Life Sciences |
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Keyword
| Immunological synapse
Cell biology
Inhibitory postsynaptic potential
Actin cytoskeleton
Actin
Biology
Cytoskeleton
Cancer cell
Cell
Chemistry
T cell
Immune system
Immunology
Neuroscience
T-cell receptor
Cancer
Biochemistry |
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Topic Classification
| Immune Cell Function and Interaction
T-cell and B-cell Immunology
CAR-T cell therapy research |
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Deposit Date
| 2025-08-05 |
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Data Type
| Article |
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Data Source
| Proceedings of the National Academy of Sciences |