Legler Daniel F, Thelen Marcus
Biotechnology Institute Thurgau (BITg), University of Konstanz, Kreuzlingen, Switzerland.
Institute for Research in Biomedicine, Università della Svizzera italiana, Bellinzona, Switzerland.
F1000Res. 2018 Jan 23;7:95. doi: 10.12688/f1000research.13130.1. eCollection 2018.
Chemokine signaling is essential for coordinated cell migration in health and disease to specifically govern cell positioning in space and time. Typically, chemokines signal through heptahelical, G protein-coupled receptors to orchestrate cell migration. Notably, chemokine receptors are highly dynamic structures and signaling efficiency largely depends on the discrete contact with the ligand. Promiscuity of both chemokines and chemokine receptors, combined with biased signaling and allosteric modulation of receptor activation, guarantees a tightly controlled recruitment and positioning of individual cells within the local environment at a given time. Here, we discuss recent insights in understanding chemokine gradient formation by atypical chemokine receptors and how typical chemokine receptors can transmit distinct signals to translate guidance cues into coordinated cell locomotion in space and time.
趋化因子信号传导对于健康和疾病状态下的细胞协调迁移至关重要,它能在特定的时间和空间内精确控制细胞定位。通常,趋化因子通过七螺旋G蛋白偶联受体发出信号,以协调细胞迁移。值得注意的是,趋化因子受体是高度动态的结构,信号传导效率很大程度上取决于与配体的离散接触。趋化因子和趋化因子受体的多特异性,再加上受体激活的偏向性信号传导和变构调节,确保了在给定时间内,单个细胞在局部环境中得到严格控制的募集和定位。在此,我们讨论了在理解非典型趋化因子受体形成趋化因子梯度方面的最新见解,以及典型趋化因子受体如何传递不同信号,从而将引导线索转化为细胞在空间和时间上的协调运动。