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The p110δ Isoform of PI3K Differentially Regulates β1 and β2 Integrin‐Mediated Monocyte Adhesion and Spreading and Modulates Diapedesis
Author(s) -
FERREIRA ALEXANDER M.,
ISAACS HAROLD,
HAYFLICK JOEL S.,
ROGERS KEM A.,
SANDIG MARTIN
Publication year - 2006
Publication title -
microcirculation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.793
H-Index - 83
eISSN - 1549-8719
pISSN - 1073-9688
DOI - 10.1080/10739680600776062
Subject(s) - wortmannin , integrin , monocyte , pi3k/akt/mtor pathway , ly294002 , microbiology and biotechnology , cell adhesion , chemistry , adhesion , biology , signal transduction , receptor , biochemistry , cell , immunology , organic chemistry
Objective: Leukocyte diapedesis is misregulated in inflammatory disease and depends on the binding of monocytic LFA‐1 and VLA‐4 to endothelial ICAM‐1 and VCAM‐1, respectively. The authors hypothesized that these different molecular interactions elicit specific signaling cascades within monocytes regulating specific steps in adhesion, motility, and diapedesis. Methods: The authors employed the PI3K p110δ catalytic subunit specific inhibitor IC87114 (2 μ M) and the broad‐spectrum PI3K inhibitory agents LY294002 (50 μ M) and wortmannin (100 nM), to examine the role of PI3Kδ in monocyte diapedesis through endothelial monolayers and its role in monocyte adhesion and spreading upon carpets of ICAM‐1 or VCAM‐1. They further explored the effects of PI3Kδ inhibition on the activation state of β 1 and β 2 integrins with immunocytochemistry and flow cytometry. Results: In human peripheral blood monocytes IC87114 was as effective as wortmannin and LY294002 at inhibiting diapedesis, however, in THP‐1 cells LY294002 and wortmannin caused a 5‐fold reduction in diapedesis, while IC87114 only decreased diapedesis 2‐fold. PI3Kδ activity was specifically required for THP‐1 cell adhesion and spreading on VCAM‐1, but not on ICAM‐1 protein substrates. Flow cytometric analysis demonstrated that PI3Kδ inhibition decreased the amount of conformationally active β 1‐integrins, while having no effect on the prevalence of conformationally active β 2‐integrins expressed on the cell surface. In addition, PI3Kδ inhibition resulted in a 4‐fold decrease in the activation state of Rac‐1 and Cdc42. Conclusions: These results demonstrate the specific necessity of PI3Kδ in regulating monocytic integrin activation and the general role of PI3K signaling during diapedesis, implicating PI3K as a target for therapeutic intervention.