Target cell cortical tension regulates macrophage trogocytosis
Macrophages are known to engulf small membrane fragments, or trogocytose, target cells and pathogens, rather than fully phagocytose them. However, little is known about what causes macrophages to choose trogocytosis versus phagocytosis. Here we report that cortical tension of target cells is a key regulator of macrophage trogocytosis. At low tension, macrophages will preferentially trogocytose antibody-opsonized cells, while at high tension, they tend towards phagocytosis. Using model vesicles, we demonstrate that macrophages will rapidly switch from trogocytosis to phagocytosis when membrane tension is increased. Stiffening the cortex of target cells also biases macrophages to phagocytose them, a trend that can be countered by increasing antibody surface density and is captured in a mechanical model of trogocytosis. This work suggests that the target cell, rather than the macrophage, determines whether phagocytosis or trogocytosis occurs, and that macrophages do not require a distinct molecular pathway for trogocytosis.
Authors
- Lucia Baldauf (ORCID: https://orcid.org/0000-0001-5200-4044)
- Caitlin E. Cornell (ORCID: https://orcid.org/0000-0001-7675-1415)
- Deepak Krishnamurthy (ORCID: https://orcid.org/0000-0002-4504-1530)
- Aymeric Chorlay (ORCID: https://orcid.org/0000-0002-8759-3616)
- Daniel A. Fletcher (ORCID: https://orcid.org/0000-0002-1890-5364)
- Nicolle Martin
Institutions
- QB3 (US)
- Lawrence Berkeley National Laboratory (US)
- University of California, San Francisco (US)
- London Centre for Nanotechnology (GB)
- Chan Zuckerberg Initiative (United States) (US)
- University College London (GB)
- University of California, Berkeley (US)
Publication Details
- Journal
- Nature Cell Biology
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1038/s41556-025-01807-6
- Citations
- 2
- Primary Topic
- Phagocytosis and Immune Regulation
- Type
- article
- Field-Weighted Citation Impact
- 1.59
Funders
- National Science Foundation
- Cancer Research Institute
- James S. McDonnell Foundation
- National Institutes of Health