吞噬作用
巨噬细胞
细胞生物学
生物
化学
生物化学
体外
作者
Caitlin E. Cornell,Aymeric Chorlay,Deepak Krishnamurthy,Nicolle Martin,Lucia Baldauf,Daniel A. Fletcher
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2024-12-05
被引量:5
标识
DOI:10.1101/2024.12.02.626490
摘要
Summary 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 a distinct molecular pathway for trogocytosis is not required to explain differences in trogocytosis among target cell types and points to a mechanism for target cells to modulate trogocytosis.
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