PSGL-1-dependent myeloid leukocyte activation
- Alexander Zarbock(corresponding author),
- Helena Müller,
- Yoshihiro Kuwano,
- University of Münster,
- Max Planck Institute for Molecular Biomedicine,
- La Jolla Institute for Allergy and Immunology,
- ,
- ,
Open access
Abstract
Cell-cell interactions mediating leukocyte recruitment and inflammation are crucial for host defense. Leukocyte recruitment into injured tissue proceeds in a multistep process. The first contact of leukocytes with endothelial cells ("capturing" or "tethering") is mediated by selectins and their counter-receptor P-selectin glycoprotein ligand (PSGL)-1. During capture and rolling, leukocytes collect different inflammatory signals, which can activate various pathways. Integration of these signals leads to leukocyte activation, integrin-mediated arrest, cytoskeleton rearrangement, polarization, and transmigration. PSGL-1 on leukocytes also binds to activated platelets, where P-selectin is expressed at locally high site densities following α-granule fusion with the plasma membrane. Here, we review the signaling functions of PSGL-1 and speculate how the different known signaling events might relate to different phases of leukocyte recruitment.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 1119-1124 (6 pages)Journal (Volume, Issue Number)
Journal of Leukocyte Biology (Volume 86, Issue 5)Publication milestones
- Published - 11/2009
Publication status
ISSN
0741-5400Publication IDs
- Scopus: 70350736130
- PubMed: 19703898
