Article abstract
Nature Immunology 8, 882 - 892 (2007)
Published online: 15 July 2007 | doi:10.1038/ni1491
P-selectin primes leukocyte integrin activation during inflammation
Hai-Bo Wang1,4, Jin-Tao Wang1,4, Lei Zhang1,4, Zhen H Geng2,4, Wei-Li Xu1,4, Tao Xu1,4, Yuqing Huo2, Xueliang Zhu1, Edward F Plow3, Ming Chen1 & Jian-Guo Geng1,2
Abstract
Selectins mediate leukocyte rolling and prime leukocytes for integrin-mediated leukocyte adhesion. However, neither the in vivo importance of nor the signaling pathway by which selectin-mediated integrin activation occurs has been determined. We report here that P-selectin-deficient mice manifested impaired leukocyte adhesion, which was 'rescued' by soluble P-selectin. Mechanistically, the cytoplasmic domain of P-selectin glycoprotein ligand 1 formed a constitutive complex with Nef-associated factor 1. After binding of P-selectin, Src kinases phosphorylated Nef-associated factor 1, which recruited the phosphoinositide-3-OH kinase p85-p110
heterodimer and resulted in activation of leukocyte integrins. Inhibition of this signal-transduction pathway diminished the adhesion of leukocytes to capillary venules and suppressed peritoneal infiltration of leukocytes. Our data demonstrate the functional importance of this newly identified signaling pathway mediated by P-selectin glycoprotein ligand 1.
- Laboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, The Graduate School of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
- Vascular Biology Center, Divisions of Hematology, Oncology and Transplantation and Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
- Department of Molecular Cardiology, Joseph J. Jacobs Center for Thrombosis and Vascular Biology, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
- These authors contributed equally to this work.
Correspondence to: Jian-Guo Geng1,2 e-mail: genglab@gmail.com
Correspondence to: Ming Chen1 e-mail: chenm@sibs.ac.cn
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