Torres Alexis J, Holowka David, Baird Barbara A
Department of Chemistry and Chemical Biology,Cornell University, Ithaca, NY, USA.
Methods Mol Biol. 2011;748:195-207. doi: 10.1007/978-1-61779-139-0_14.
Fc receptor signaling plays a fundamental role in immune responses. A plethora of Fc -receptors (e.g., Fc gamma, Fc-alpha, and Fc-epsilon) are expressed on different immune cells, including natural killer cells, macrophages, mast cells, and neutrophils. Receptor clustering and activation by multivalent ligands or opsonized particles induce a signaling cascade that leads to targeted secretion of chemical mediators (i.e., histamine, cytokines, and chemokines) and phagocytosis, among other responses. Spatial targeting and compartmentalization are common mechanisms of regulation in Fc receptor signaling. However, the tools for studying these dynamic interactions have been limited. To overcome these limitations in our model system, microfabricated surfaces containing spatially defined ligands are used to cluster- and activate IgE receptors (FcεRI), involved in allergic responses by mast cells. Micron-scale control of cell activation allows investigation of spatially regulated mechanisms for intracellular signaling with -fluorescence microscopy. This approach in conjunction with biochemical techniques has proven to be valuable for investigating immune receptor signaling.
Fc受体信号传导在免疫反应中起着基础性作用。大量的Fc受体(如Fcγ、Fcα和Fcε)在不同的免疫细胞上表达,包括自然杀伤细胞、巨噬细胞、肥大细胞和中性粒细胞。多价配体或调理素化颗粒诱导的受体聚集和激活会引发信号级联反应,导致化学介质(如组胺、细胞因子和趋化因子)的靶向分泌以及吞噬作用等其他反应。空间靶向和区室化是Fc受体信号传导中常见的调节机制。然而,用于研究这些动态相互作用的工具一直很有限。为了在我们的模型系统中克服这些限制,使用含有空间定义配体的微加工表面来聚集和激活参与肥大细胞过敏反应的IgE受体(FcεRI)。细胞激活的微米级控制允许通过荧光显微镜研究细胞内信号传导的空间调节机制。这种方法与生化技术相结合已被证明对研究免疫受体信号传导很有价值。