Neutrophils scan for activated platelets to initiate inflammation

Author:

Sreeramkumar Vinatha1,Adrover José M.1,Ballesteros Ivan2,Cuartero Maria Isabel2,Rossaint Jan3,Bilbao Izaskun14,Nácher Maria15,Pitaval Christophe1,Radovanovic Irena1,Fukui Yoshinori6,McEver Rodger P.7,Filippi Marie-Dominique8,Lizasoain Ignacio2,Ruiz-Cabello Jesús14,Zarbock Alexander3,Moro María A.2,Hidalgo Andrés19

Affiliation:

1. Department of Atherothrombosis, Imaging and Epidemiology, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.

2. Unidad de Investigación Neurovascular, Department of Pharmacology, Faculty of Medicine, Universidad Complutense and Instituto de Investigación Hospital 12 de Octubre (i+12), Madrid, Spain.

3. Department of Anesthesiology and Critical Care Medicine, University of Münster and Max Planck Institute Münster, Münster, Germany.

4. Ciber de Enfermedades Respiratorias (CIBERES), Madrid, Spain.

5. Faculty of Science, Medicine and Health, University of Wollongong, New South Wales, Australia.

6. Division of Immunogenetics, Department of Immunobiology and Neuroscience, Kyushu University, Japan.

7. Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.

8. Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Research Foundation, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

9. Institute for Cardiovascular Prevention, Ludwig-Maximilians-University, Munich, Germany.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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