Institute for Research in Biomedicine, Università della Svizzera italiana, Bellinzona, Switzerland.
Biotechnology Institute Thurgau (BITg) at the University of Konstanz, Kreuzlingen, Switzerland.
Cytokine. 2018 Sep;109:72-75. doi: 10.1016/j.cyto.2018.02.011. Epub 2018 Feb 9.
Migration of leukocytes is typically mediated by G protein-coupled receptors (GPCRs) upon activation by specific ligands that range from small peptides, chemokines to a variety of lipidic molecules. The heptahelical receptors are highly dynamic structures and the signaling efficiency largely depends on the discrete contact with the ligand. In addition, several allosteric modulators of receptor activity have been reported, which do not induce migration by themselves. Another important mechanism modulating the activity of GPCRs is their local environment. Not only the membrane lipid composition influences the activity, but also direct binding of lipids, in particular cholesterol, was shown to alter receptor signaling properties. Recent findings indicate that also chemokine receptor activity is modulated by membrane lipids. In this short review we discuss this new paradigm and potential consequences for chemokine-induced migration.
白细胞的迁移通常是由 G 蛋白偶联受体 (GPCRs) 介导的,这些受体在受到特定配体的激活后会发生迁移,这些配体的范围从小肽、趋化因子到各种脂质分子。七螺旋受体是高度动态的结构,信号效率在很大程度上取决于与配体的离散接触。此外,已经报道了几种受体活性的变构调节剂,它们本身不会诱导迁移。另一个调节 GPCR 活性的重要机制是它们的局部环境。不仅膜脂质组成会影响活性,而且脂质的直接结合,特别是胆固醇,被证明会改变受体的信号转导特性。最近的发现表明,趋化因子受体的活性也受到膜脂质的调节。在这篇简短的综述中,我们讨论了这一新的范例及其对趋化因子诱导迁移的潜在影响。