炎症
血小板
受体
细胞生物学
血小板活化
封锁
免疫系统
内皮
免疫学
生物
化学
内分泌学
生物化学
作者
Vinatha Sreeramkumar,José M. Adrover,Iván Ballesteros,María Isabel Cuartero,Jan Rossaint,Izaskun Bilbao,María Nácher,Christophe Pitaval,Irena Radovanovic,Yoshinori Fukui,Rodger P. McEver,Marie-Dominique Filippi,Ignacio Lizasoaín,Jesús Ruíz‐Cabello,Alexander Zarbock,Marı́a A. Moro,Andrés Hidalgo
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2014-12-04
卷期号:346 (6214): 1234-1238
被引量:575
标识
DOI:10.1126/science.1256478
摘要
Immune and inflammatory responses require leukocytes to migrate within and through the vasculature, a process that is facilitated by their capacity to switch to a polarized morphology with an asymmetric distribution of receptors. We report that neutrophil polarization within activated venules served to organize a protruding domain that engaged activated platelets present in the bloodstream. The selectin ligand PSGL-1 transduced signals emanating from these interactions, resulting in the redistribution of receptors that drive neutrophil migration. Consequently, neutrophils unable to polarize or to transduce signals through PSGL-1 displayed aberrant crawling, and blockade of this domain protected mice against thromboinflammatory injury. These results reveal that recruited neutrophils scan for activated platelets, and they suggest that the neutrophils' bipolarity allows the integration of signals present at both the endothelium and the circulation before inflammation proceeds.
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