aureus and S pneumoniae, resulting in elevated TNF and IL-10 sec

aureus and S. pneumoniae, resulting in elevated TNF and IL-10 secretion and diminished IL-12 levels (Fig. 1C). Since IRAK4 is a key signaling adaptor in the TLR pathway but whole pathogens represent complex mixtures of multiple PRR ligands we sought to perform experiments

with defined TLR ligands to better assess the role of IRAK4. We therefore analyzed cytokine secretion in response to synthetic TLR2 ligand Pam3CSK4 and TLR4 agonist LPS. Consistent with the observations made in monocytes of IRAK4-deficient patients [23], down-regulation of IRAK4 lead to a reduction of TNF secretion levels in response to LPS (Fig. 2A). Similarly, LPS-induced production of IL-12 (Fig. 2A), Daporinad IL-6, and IL-1β (not shown) was diminished in IRAK4-deficient cells. Similarly, secretion of TNF and IL-12 in IRAK4-silenced cells was markedly

decreased after Pam3CSK4 stimulation Selleck KU-60019 (Fig. 2B). Of note, differences in cytokine concentrations were not statistically significant in all cases, but, despite donor-dependent variation in the cytokine levels, the trend was clear in all donors and experiments shown. To further confirm the specificity of our siRNA knockdown, we next studied TLR-induced TNF production in the presence or absence of a commercially available IRAK1/4 inhibitor. As expected, both LPS and Pam3CSK4-induced TNF secretion was reduced under IRAK1/4 inhibition (Fig. 2C). Finally, we analyzed activation of NF-κB subunits p50 and p65. These transcription factors form part of the classical NF-κB pathway and are activated upon TLR

stimulation. Confirming our earlier observations LPS-triggered induction of p50 as well as p65 was decreased in IRAK4-knockdown selleck products cells when compared with that in cells transfected with unspecific control siRNA (Fig. 2D), thus highlighting the key role of IRAK4 in mediating NF-κB-dependent pro-inflammatory cytokine secretion. Having confirmed that TLR-triggered pro-inflammatory cytokine production is decreased under IRAK4 knockdown conditions we analyzed the release of anti-inflammatory IL-10. As already observed using live bacteria (Fig. 1C), we found that IL-10 levels were markedly increased after LPS and Pam3CSK4 stimulation in IRAK4-deficient cells (Fig. 3A). Elevated IL-10 secretion and specificity of the knockdown was again confirmed with the IRAK1/4 inhibitor (Fig. 3B). Further analysis demonstrated increased IL-10 mRNA expression under IRAK4-silencing conditions (Fig. 3C), thus indicating that increases in IL-10 protein levels are due to enhanced gene transcription. Not surprisingly, elevated IL-10 levels were accompanied by increased mRNA expression of the IL-10-dependent genes socs3 and tnfr2 (Fig. 3C) while that of others such as stat3 or CREB-dependent cox2 was unaffected (data not shown).

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