Edinburgh Research Explorer

Phosphoinositide 3-OH Kinase Regulates Integrin-Dependent Processes in Neutrophils by Signaling through Its Effector ARAP3

Research output: Contribution to journalArticle

  • Laure Gambardella
  • Karen E Anderson
  • Zoltán Jakus
  • Miklós Kovács
  • Susann Voigt
  • Phillip T Hawkins
  • Len Stephens
  • Attila Mócsai
  • Sonja Vermeren

Related Edinburgh Organisations

Open Access permissions

Open

Documents

  • Download as Adobe PDF

    Rights statement: Published in final edited form as: J Immunol. Jan 1, 2013; 190(1): 381–391. Published online Nov 23, 2012. doi: 10.4049/jimmunol.1201330

    Accepted author manuscript, 1 MB, PDF-document

http://www.jimmunol.org/content/190/1/381
Original languageEnglish
Pages (from-to)381-91
Number of pages11
JournalJournal of Immunology
Volume190
Issue number1
DOIs
Publication statusPublished - 2013

Abstract

ARAP3, a GTPase activating protein for Rho and Arf family GTPases, is one of many phosphoinositide 3-OH kinase (PI3K) effectors. In this study, we investigate the regulatory input of PI3K upstream of ARAP3 by analyzing neutrophils from an ARAP3 pleckstrin homology (PH) domain point mutation knock-in mouse (R302, 303A), in which ARAP3 is uncoupled from activation by PI3K. ARAP3 PH domain point mutant neutrophils are characterized by disturbed responses linked to stimulation by either integrin ligands or immobilized immune complexes. These cells exhibit increased β2 integrin inside-out signaling (binding affinity and avidity), and our work suggests the disturbed responses to immobilized immune complexes are secondary to this. In vitro, neutrophil chemotaxis is affected in the mutant. In vivo, ARAP3 PH domain point mutant bone marrow chimeras exhibit reduced neutrophil recruitment to the peritoneum on induction of sterile peritonitis and also reduced inflammation in a model for rheumatoid arthritis. The current work suggests a dramatic regulatory input of PI3K into the regulation of β2 integrin activity, and processes dependent on this, by signaling through its effector ARAP3.

Download statistics

No data available

ID: 5555698