CRUK Scotland Institute, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Department of Cell and Developmental Biology, University College London, London, UK.
Methods Mol Biol. 2024;2828:1-9. doi: 10.1007/978-1-0716-4023-4_1.
Immune responses rely on efficient and coordinated migration of immune cells to the site of infection or injury. To reach the site of immunological threat often requires long-range navigation of immune cells through complex tissue and vascular networks. Chemotaxis, cell migration steered by gradients of cell-attractive chemicals that bind sensory receptors, is central to this response. Chemoattractant receptors mostly belong to the G-protein-coupled receptor (GPCR) family, but the way attractant-receptor signaling directs cell migration is not fully understood. Direct-viewing chemotaxis chambers combined with time-lapse microscopy give a powerful tool to study the dynamic details of cells' responses to different attractant landscapes. Here, we describe the application of one such chamber (the Dunn chamber) to study bone marrow-derived macrophage chemotaxis to gradients of complement C5a.
免疫反应依赖于免疫细胞高效协调地迁移到感染或损伤部位。为了到达免疫威胁的部位,免疫细胞通常需要通过复杂的组织和血管网络进行长距离导航。趋化作用,即细胞在吸引化学物质梯度的引导下迁移,是这种反应的核心。趋化因子受体主要属于 G 蛋白偶联受体 (GPCR) 家族,但趋化因子受体信号引导细胞迁移的方式还不完全清楚。直视趋化性室结合延时显微镜为研究细胞对不同趋化因子景观的动态反应提供了强大的工具。在这里,我们描述了这种趋化性室(Dunn 室)在研究骨髓来源的巨噬细胞向补体 C5a 梯度趋化性中的应用。