Department of Physiology, Development and Neuroscience, University of Cambridge.
Department of Physiology, Development and Neuroscience, University of Cambridge;
J Vis Exp. 2020 Dec 4(166). doi: 10.3791/61679.
Leukocyte guidance by chemical gradients is essential for immune responses. Neutrophils are the first cells to be recruited to sites of tissue damage where they execute crucial antimicrobial functions. Their trafficking to these loci is orchestrated by several inflammatory chemoattractants, including chemokines. At the molecular level, chemoattractant signaling is regulated by the intracellular trafficking of the corresponding receptors. However, it remains unclear how subcellular changes in chemokine receptors affect leukocyte migration dynamics at the cell and tissue level. Here we describe a methodology for live imaging and quantitative analysis of chemokine receptor dynamics in neutrophils during inflammatory responses to tissue damage. These tools have revealed that differential chemokine receptor trafficking in zebrafish neutrophils coordinates neutrophil clustering and dispersal at sites of tissue damage. This has implications for our understanding of how inflammatory responses are self-resolved. The described tools could be used to understand neutrophil migration patterns in a variety of physiological and pathological settings and the methodology could be expanded to other signaling receptors.
白细胞通过化学梯度的导向对于免疫反应至关重要。中性粒细胞是首先被招募到组织损伤部位的细胞,在那里它们执行关键的抗菌功能。它们向这些部位的迁移是由几种炎症趋化因子协调的,包括趋化因子。在分子水平上,趋化因子信号受相应受体的细胞内运输调节。然而,趋化因子受体的亚细胞变化如何影响细胞和组织水平上白细胞迁移的动力学仍不清楚。在这里,我们描述了一种用于在炎症反应过程中实时成像和定量分析中性粒细胞中趋化因子受体动力学的方法。这些工具揭示了斑马鱼中性粒细胞中差异趋化因子受体的运输协调了组织损伤部位中性粒细胞的聚集和分散。这对我们理解炎症反应如何自我解决具有重要意义。所描述的工具可用于理解各种生理和病理状态下的中性粒细胞迁移模式,并且该方法可以扩展到其他信号受体。