Medical Journals

Alpha-chain Phosphorylation of the Human Leukocyte Cd11b/Cd18 (Mac-1) Integrin is Pivotal for Integrin Activation to Bind Icams and Leukocyte Extravasation.

Authors:
  • Fagerholm Susanna C
  • Varis Minna
  • Stefanidakis Michael
  • Hilden Tiina J
  • Gahmberg Carl G

From: Division of Biochemistry, Faculty of Biosciences, PB56 (Viikinkaari 5), 00014 University of Helsinki, Helsinki, Finland.

Blood

  • Publish Date: Nov 2006
  • ISSN: 0006-4971
  • Volume: 108
  • Issue: 10
  • Pages: 3379-86
  • Medium: Print
  • Language: English
  • Citation (JAMA): Fagerholm Susanna C, Varis Minna, Stefanidakis Michael, et al. Alpha-chain Phosphorylation of the Human Leukocyte Cd11b/Cd18 (Mac-1) Integrin is Pivotal for Integrin Activation to Bind Icams and Leukocyte Extravasation.. Blood Nov 2006;108:3379-86

Abstract

The promiscuous CD11b/CD18 (Mac-1) integrin has important roles in regulating many immunologic functions such as leukocyte adhesion and emigration from the bloodstream via interactions with the endothelial ligands ICAM-1 and ICAM-2, iC3b-mediated phagocytosis, and apoptosis. However, the mechanisms for Mac-1 inside-out activation have remained poorly understood. Phosphorylation of integrin cytoplasmic domains is emerging as an important mechanism of regulating integrin functions. Here, we have studied phosphorylation of human CD11b, which takes place on the cytoplasmic Ser1126 in neutrophils. We show that mutation of the serine phosphorylation site leads to inability of Mac-1 to become activated to bind the cellular ligands ICAM-1 and ICAM-2. However, CD11b-mutant cells are fully capable of binding other studied CD11b ligands (ie, iC3b and denatured BSA). Activation epitopes expressed in the extracellular domain of the integrin and affinity for soluble ICAM ligands were decreased for the mutated integrin. Additionally, the mutation resulted in inhibition of chemokine-induced migration in a transendothelial assay in vitro and significantly reduced the accumulation of intravenously administered cells in the spleen and lungs of Balb/c mice. These results characterize a novel selective mechanism of Mac-1-integrin activation, which mediates leukocyte emigration from the bloodstream to the tissues.

Mesh Headings (Keywords): Animals, Antigens, CD, Antigens, CD11b, Antigens, CD18, Binding Sites, Cell Adhesion Molecules, Chemotaxis, Leukocyte, Humans, Integrins, Intercellular Adhesion Molecule-1, Leukocytes, Macrophage-1 Antigen, Mice, Mice, Inbred BALB C, Mutation, Phosphorylation, Serine


Check for Full Text / PubMed Unique Identifier (PMID): 16857989


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.