Center for Engineering Mechanobiology, University of Pennsylvania, Philadelphia, PA, 19104, USA.
CAS Key Laboratory of Mechanical Behavior and Design of Materials, Department of Modern Mechanics, University of Science and Technology of China, Hefei, Anhui, 230027, China.
Nat Commun. 2023 May 22;14(1):2902. doi: 10.1038/s41467-023-38598-z.
Immune cells, such as macrophages and dendritic cells, can utilize podosomes, mechanosensitive actin-rich protrusions, to generate forces, migrate, and patrol for foreign antigens. Individual podosomes probe their microenvironment through periodic protrusion and retraction cycles (height oscillations), while oscillations of multiple podosomes in a cluster are coordinated in a wave-like fashion. However, the mechanisms governing both the individual oscillations and the collective wave-like dynamics remain unclear. Here, by integrating actin polymerization, myosin contractility, actin diffusion, and mechanosensitive signaling, we develop a chemo-mechanical model for podosome dynamics in clusters. Our model reveals that podosomes show oscillatory growth when actin polymerization-driven protrusion and signaling-associated myosin contraction occur at similar rates, while the diffusion of actin monomers drives wave-like coordination of podosome oscillations. Our theoretical predictions are validated by different pharmacological treatments and the impact of microenvironment stiffness on chemo-mechanical waves. Our proposed framework can shed light on the role of podosomes in immune cell mechanosensing within the context of wound healing and cancer immunotherapy.
免疫细胞,如巨噬细胞和树突状细胞,可以利用足突,即机械敏感的富含肌动蛋白的突起,产生力、迁移和巡逻以寻找外来抗原。单个足突通过周期性的突起和回缩循环(高度振荡)来探测其微环境,而簇中的多个足突的振荡则以波浪式的方式协调。然而,控制单个振荡和集体波状动力学的机制仍不清楚。在这里,我们通过整合肌动蛋白聚合、肌球蛋白收缩、肌动蛋白扩散和机械敏感信号,为簇中的足突动力学开发了一个化学生物力学模型。我们的模型表明,当肌动蛋白聚合驱动的突起和信号相关的肌球蛋白收缩以相似的速度发生时,足突表现出振荡生长,而肌动蛋白单体的扩散则驱动足突振荡的波浪式协调。我们的理论预测通过不同的药理学处理和微环境刚度对化学生物波的影响得到了验证。我们提出的框架可以揭示足突在创伤愈合和癌症免疫治疗背景下免疫细胞机械感觉中的作用。