ReviewNature protocols2026
Using tunable hydrogel microparticles to measure cellular forces.
Review in Nature protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Myo1e/f regulate phagocytic podosomes to promote efficient cup closure in macrophages.bioRxiv : the preprint server for biology · 2026Article
- From biting to engulfment: curvature-actin coupling controls phagocytosis of soft, deformable targets.bioRxiv : the preprint server for biology · 2026Article
- From biting to engulfment: curvature-actin coupling controls phagocytosis of soft, deformable targets.ArXiv · 2026Article
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Force generation is an integral part of cellular behavior. It plays a crucial role in cell adhesion, migration and division. Mechanical forces are also essential in cell-to-cell interactions, including the widespread interactions involving immune cells. Accurately measuring these forces remains a major challenge, yet it is essential for understanding the mechanobiological mechanisms driving these interactions. Here, we describe a methodology in which deformable and tunable hydrogel microparticles are used to quantify cellular forces. A specific type of acrylamide-based tunable hydrogel microparticles, deformable poly-acrylamide co-acrylic acid microparticles (DAAM-particles), are synthesized in batch using a membrane emulsification approach and conjugated with both biologically active molecules and fluorescent labels through a one-pot functionalization procedure. Cells are then incubated with functionalized DAAM-particles and imaged by confocal microscopy. With a custom image-analysis strategy, local microparticle deformations can be quantified with super-resolution accuracy (<50 nm). Elasticity theory calculations allow for the inference of normal and shear forces, revealing the direction and spatial distribution of cellular forces. The tunability of DAAM-particles enables their adaptation for investigating numerous cellular processes, making them a valuable tool for understanding mechanobiology. The entire protocol takes 2-3 d, requires only basic expertise in mammalian cell culture and fluorescence microscopy and utilizes less specialized equipment and facilities compared with other available techniques. As an example, we demonstrate how this methodology can reveal actin-based force generation during phagocytosis by macrophages.
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Registered trials
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