Antibody Fc receptor CD16a mediates natural killer cell activation via mechanotransduction of piconewton forces

Natural Killer(NK) cells eliminate target cells through antibody-dependent cell-mediated cytotoxicity(ADCC), initiated by CD16a(FcγRIIIa) recognizing the Fc region of antibodies bound to the target cell surface. While the recognition is considered to be driven by CD16a-Fc binding avidity, it fails to explain why Fc multimers inhibit ADCC rather than trigger it. Here, we reveal that CD16a transduces piconewton forces, and acts as a mechanosensor to facilitate NK activation. We demonstrate that CD16a force and the actin foci formation associated with it are essential for the phosphorylation of mechanosensitive adaptor Cas-L and signaling adaptor LAT, reshaping NK cell cytoskeletal dynamics and signaling. Our findings show that NK activation is an intricate process that integrates both biochemical and biophysical information, and provides new mechanistic insight for immunoengineering.

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Publication Details

Journal
Science Advances
Published
2026-08-28
DOI
https://doi.org/10.1126/sciadv.aeb8946
Citations
2
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
12.35

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article

Antibody Fc receptor CD16a mediates natural killer cell activation via mechanotransduction of piconewton forces

Bianxiao Cui, Markus W. Covert, Rong Ma, K. Christopher Garcia et al.
2 citations
Science Advances
Monoclonal and Polyclonal Antibodies Research
12.35
article

Antibody Fc receptor CD16a mediates natural killer cell activation via mechanotransduction of piconewton forces

Bianxiao Cui, Markus W. Covert, Rong Ma, K. Christopher Garcia, Rong Ma
article en
2 citations

Abstract

Natural Killer(NK) cells eliminate target cells through antibody-dependent cell-mediated cytotoxicity(ADCC), initiated by CD16a(FcγRIIIa) recognizing the Fc region of antibodies bound to the target cell surface. While the recognition is considered to be driven by CD16a-Fc binding avidity, it fails to explain why Fc multimers inhibit ADCC rather than trigger it. Here, we reveal that CD16a transduces piconewton forces, and acts as a mechanosensor to facilitate NK activation. We demonstrate that CD16a force and the actin foci formation associated with it are essential for the phosphorylation of mechanosensitive adaptor Cas-L and signaling adaptor LAT, reshaping NK cell cytoskeletal dynamics and signaling. Our findings show that NK activation is an intricate process that integrates both biochemical and biophysical information, and provides new mechanistic insight for immunoengineering.

Science AdvancesVol. 12(35)
Howard Hughes Medical Institute (US), Neurosciences Institute (US), Stanford University (US)
Howard Hughes Medical Institute, Stanford University, Michelson Prize and Grants, National Institutes of Health
Openalex Percentile: Top 2%
Monoclonal and Polyclonal Antibodies Research
12.35
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