Human S100A9 potentiates IL-8 production in response to GM-CSF or fMLP via activation of a different set of transcription factors in neutrophils.

Abstract:

:Inflammation is highly regulated by various agents. Unexpectedly, we report here that the damage-associated molecular pattern S100A9 protein, a potent neutrophil activator and inducer of cytokine production in monocytes, is not a direct activator of cytokine production in human neutrophils. However, S100A9 primed IL-8 production in fMLP- and GM-CSF-stimulated neutrophiles via NF-κB and CREB-1, and NF-κB, STAT3 and STAT5, respectively. Pharmacological inhibition confirmed the importance of these transcription factors by significantly decreasing IL-8 production. This is the first time that a different set of transcription factors are shown to be involved in S100A9-primed neutrophils in response to proinflammatory agonist.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Simard JC,Noël C,Tessier PA,Girard D

doi

10.1016/j.febslet.2014.04.027

subject

Has Abstract

pub_date

2014-06-13 00:00:00

pages

2141-6

issue

13

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(14)00313-5

journal_volume

588

pub_type

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