Chemotaxis Signaling Section, Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, NIH, Rockville, MD 20852
Chemotaxis Signaling Section, Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, NIH, Rockville, MD 20852.
Proc Natl Acad Sci U S A. 2021 Oct 26;118(43). doi: 10.1073/pnas.2002162118.
Neutrophils sense and migrate through an enormous range of chemoattractant gradients through adaptation. Here, we reveal that in human neutrophils, calcium-promoted Ras inactivator (CAPRI) locally controls the GPCR-stimulated Ras adaptation. Human neutrophils lacking CAPRI ( ) exhibit chemoattractant-induced, nonadaptive Ras activation; significantly increased phosphorylation of AKT, GSK-3α/3β, and cofilin; and excessive actin polymerization. cells display defective chemotaxis in response to high-concentration gradients but exhibit improved chemotaxis in low- or subsensitive-concentration gradients of various chemoattractants, as a result of their enhanced sensitivity. Taken together, our data reveal that CAPRI controls GPCR activation-mediated Ras adaptation and lowers the sensitivity of human neutrophils so that they are able to chemotax through a higher-concentration range of chemoattractant gradients.
中性粒细胞通过适应感知和迁移范围巨大的趋化因子梯度。在这里,我们揭示了人类中性粒细胞中,钙促进 Ras 失活蛋白(CAPRI)局部控制 GPCR 刺激的 Ras 适应。缺乏 CAPRI 的人类中性粒细胞( )表现出趋化因子诱导的非适应性 Ras 激活;显著增加 AKT、GSK-3α/3β 和丝切蛋白的磷酸化;以及过度的肌动蛋白聚合。 细胞对高浓度梯度的趋化作用表现出缺陷,但对各种趋化因子的低浓度或亚敏感浓度梯度的趋化作用表现出改善,这是由于它们的敏感性增强。总之,我们的数据表明 CAPRI 控制 GPCR 激活介导的 Ras 适应,并降低人类中性粒细胞的敏感性,使它们能够通过更高浓度范围的趋化因子梯度趋化。