Sklar L A, Omann G M
Department of Immunology, Scripps Clinic and Research Foundation, La Jolla, CA 92037.
Semin Cell Biol. 1990 Apr;1(2):115-23.
Neutrophil activation and adaptation are beginning to be understood in quantitative and mechanistic detail. Neutrophil responses to chemoattractants involve cell surface receptors, guanine nucleotide binding (G) proteins and intracellular second messengers which are generated within a few seconds of the presentation of the ligand. Novel real-time fluorescent methods have made it possible to examine the dynamics of assembly and disassembly of receptors and G proteins during cell activation and to model, by computer, the complex sequence of ligand-receptor events. Rapid amplification cascades of signals are observed in both stimulatory and inhibitory receptor pathways. The adaptation of neutrophils involves uncoupling between receptors and G proteins, both by sequestering receptors from the transduction sequence and by reducing the activatibility of the G proteins.
中性粒细胞的激活和适应性正开始在定量和机制细节方面得到理解。中性粒细胞对趋化因子的反应涉及细胞表面受体、鸟嘌呤核苷酸结合(G)蛋白和细胞内第二信使,这些在配体呈现后的几秒钟内产生。新型实时荧光方法使得在细胞激活过程中研究受体和G蛋白组装与拆卸的动力学成为可能,并通过计算机对配体-受体事件的复杂序列进行建模。在刺激性和抑制性受体途径中均观察到信号的快速放大级联反应。中性粒细胞的适应性涉及受体与G蛋白之间的解偶联,这既通过将受体从转导序列中隔离,也通过降低G蛋白的激活能力来实现。