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2018 ; 9
(ä): 279
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K63-Linked Polyubiquitination on TRAF6 Regulates LPS-Mediated MAPK Activation,
Cytokine Production, and Bacterial Clearance in Toll-Like Receptor 7/8 Primed
Murine Macrophages
#MMPMID29515583
Talreja J
; Samavati L
Front Immunol
2018[]; 9
(ä): 279
PMID29515583
show ga
Post viral infection bacterial pneumonia is a major cause of morbidity and
mortality associated with both seasonal and pandemic influenza virus illness.
Despite much efforts put into the discovery of mechanisms of post viral-bacterial
infections and their complications in recent years, the molecular mechanisms
underlying the increased susceptibility to bacterial infection remain poorly
understood. In this study, we focused on the pathways regulating immune responses
in murine macrophages and modeled post viral-bacterial infections through
pretreatment of bone marrow-derived macrophages (BMDMs) with a toll-like receptor
(TLR) 7/8 ligand (R848) and subsequent challenge with TLR2/4 agonists to mimic
bacterial infection. We found R848-primed BMDMs upon subsequent exposure to
TLR2/4 ligands respond with enhanced inflammatory cytokine production, especially
IL-6 and TNF-?. The enhanced cytokine production in R848-primed BMDMs in response
to TLR2/4 was due to increased TGF-?-activated kinase (TAK) 1 phosphorylation
with subsequent activation of ERK and p38 MAPKs. Furthermore, we identified that
R848 priming leads to increased K63-linked polyubiquitination on TRAF6.
K63-linked polyubiquitination on TRAF6 is a signal leading to enhanced activation
of downstream pathways including TAK1. Importantly, R848-primed BMDMs infected
with live bacteria exhibited decreased bacterial clearance. Small-molecule
enhancer of rapamycin 3, an ubiquitin ligase inhibitor reversed the K63-linked
polyubiquitination on TRAF6 in R848-primed BMDMs and subsequently decreased TAK1
and MAPK phosphorylation, and cytokine production as well as reversed the
decreased bacterial clearance capacity of BMDMs. Our study may provide a novel
molecular target to alleviate post viral-bacterial infections.