Louis V. Gerstner, Jr., Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nat Commun. 2024 Sep 18;15(1):8182. doi: 10.1038/s41467-024-52453-9.
Phagocytosis is an intensely physical process that depends on the mechanical properties of both the phagocytic cell and its chosen target. Here, we employed differentially deformable hydrogel microparticles to examine the role of cargo rigidity in the regulation of phagocytosis by macrophages. Whereas stiff cargos elicited canonical phagocytic cup formation and rapid engulfment, soft cargos induced an architecturally distinct response, characterized by filamentous actin protrusions at the center of the contact site, slower cup advancement, and frequent phagocytic stalling. Using phosphoproteomics, we identified β2 integrins as critical mediators of this mechanically regulated phagocytic switch. Macrophages lacking β2 integrins or their downstream effectors, Talin1 and Vinculin, exhibited specific defects in phagocytic cup architecture and selective suppression of stiff cargo uptake. We conclude that integrin signaling serves as a mechanical checkpoint during phagocytosis to pair cargo rigidity to the appropriate mode of engulfment.
吞噬作用是一个强烈的物理过程,依赖于吞噬细胞和其选择的靶标的机械特性。在这里,我们采用具有不同变形能力的水凝胶微球来研究货物刚性在调节巨噬细胞吞噬作用中的作用。刚性货物引发了典型的吞噬杯形成和快速吞噬,而软货物则诱导了一种结构上不同的反应,其特征是在接触部位的中心有丝状肌动蛋白突起,吞噬杯推进较慢,吞噬作用经常停滞。通过磷酸化蛋白质组学,我们确定β2 整合素是这种机械调节吞噬开关的关键介质。缺乏β2 整合素或其下游效应物 Talin1 和 Vinculin 的巨噬细胞在吞噬杯结构和刚性货物摄取的选择性抑制方面表现出特定的缺陷。我们得出结论,整合素信号作为吞噬作用过程中的机械检查点,将货物刚性与适当的吞噬方式相匹配。