Activation of TAK1 by Chemotactic and Growth Factors, and Its Impact on Human Neutrophil Signaling and Functional Responses.

TitleActivation of TAK1 by Chemotactic and Growth Factors, and Its Impact on Human Neutrophil Signaling and Functional Responses.
Publication TypeJournal Article
Year of Publication2015
AuthorsSylvain-Prévost, S, Ear, T, Simard, FA, Fortin, CF, Dubois, CM, Flamand, N, McDonald, PP
JournalJ Immunol
Volume195
Issue11
Pagination5393-403
Date Published2015 Dec 01
ISSN1550-6606
KeywordsApoptosis, Cells, Cultured, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Granulocyte-Macrophage Colony-Stimulating Factor, Humans, Inflammation, Leukotrienes, MAP Kinase Kinase Kinase 1, MAP Kinase Kinase Kinase 3, MAP Kinase Kinase Kinases, MAP Kinase Signaling System, N-Formylmethionine Leucyl-Phenylalanine, Neutrophils, p38 Mitogen-Activated Protein Kinases, Phosphatidylinositol 3-Kinases, Phosphorylation, Zearalenone
Abstract

The MAP3 kinase, TAK1, is known to act upstream of IKK and MAPK cascades in several cell types, and is typically activated in response to cytokines (e.g., TNF, IL-1) and TLR ligands. In this article, we report that in human neutrophils, TAK1 can also be activated by different classes of inflammatory stimuli, namely, chemoattractants and growth factors. After stimulation with such agents, TAK1 becomes rapidly and transiently activated. Blocking TAK1 kinase activity with a highly selective inhibitor (5z-7-oxozeaenol) attenuated the inducible phosphorylation of ERK occurring in response to these stimuli but had little or no effect on that of p38 MAPK or PI3K. Inhibition of TAK1 also impaired MEKK3 (but not MEKK1) activation by fMLF. Moreover, both TAK1 and the MEK/ERK module were found to influence inflammatory cytokine expression and release in fMLF- and GM-CSF-activated neutrophils, whereas the PI3K pathway influenced this response independently of TAK1. Besides cytokine production, other responses were found to be under TAK1 control in neutrophils stimulated with chemoattractants and/or GM-CSF, namely, delayed apoptosis and leukotriene biosynthesis. Our data further emphasize the central role of TAK1 in controlling signaling cascades and functional responses in primary neutrophils, making it a promising target for therapeutic intervention in view of the foremost role of neutrophils in several chronic inflammatory conditions.

DOI10.4049/jimmunol.1402752
Alternate JournalJ. Immunol.
PubMed ID26491199
Grant List / / Canadian Institutes of Health Research / Canada