AI Article Synopsis
- This study examines how mouse bone marrow-derived macrophages respond to combined stimulation by Kdo2-lipid A (KLA) and ATP, revealing unique synergistic effects on immune response, apoptosis, and lipid metabolism compared to KLA or ATP alone.
- The research highlights the roles of key proteins like NF-kB and AP-1 in regulating cytokines, which in turn activate STAT factors that enhance immunity and promote cell death processes.
- Findings demonstrate a coordinated interaction between toll-like receptor and purinergic receptor signaling during macrophage activation, with consistent changes in gene expression and protein levels observed, contributing to our understanding of inflammatory responses in bacterial infections.
Article Abstract
Background: Macrophage activation by lipopolysaccharide and adenosine triphosphate (ATP) has been studied extensively because this model system mimics the physiological context of bacterial infection and subsequent inflammatory responses. Previous studies on macrophages elucidated the biological roles of caspase-1 in post-translational activation of interleukin-1β and interleukin-18 in inflammation and apoptosis. However, the results from these studies focused only on a small number of factors. To better understand the host response, we have performed a high-throughput study of Kdo2-lipid A (KLA)-primed macrophages stimulated with ATP.
Results: The study suggests that treating mouse bone marrow-derived macrophages with KLA and ATP produces 'synergistic' effects that are not seen with treatment of KLA or ATP alone. The synergistic regulation of genes related to immunity, apoptosis and lipid metabolism is observed in a time-dependent manner. The synergistic effects are produced by nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB) and activator protein (AP)-1 through regulation of their target cytokines. The synergistically regulated cytokines then activate signal transducer and activator of transcription (STAT) factors that result in enhanced immunity, apoptosis and lipid metabolism; STAT1 enhances immunity by promoting anti-microbial factors; and STAT3 contributes to downregulation of cell cycle and upregulation of apoptosis. STAT1 and STAT3 also regulate glycerolipid and eicosanoid metabolism, respectively. Further, western blot analysis for STAT1 and STAT3 showed that the changes in transcriptomic levels were consistent with their proteomic levels. In summary, this study shows the synergistic interaction between the toll-like receptor and purinergic receptor signaling during macrophage activation on bacterial infection.
Availability: Time-course data of transcriptomics and lipidomics can be queried or downloaded from http://www.lipidmaps.org.
Contact: shankar@ucsd.edu.
Supplementary Information: Supplementary data are available at Bioinformatics online.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799469 | PMC |
| http://dx.doi.org/10.1093/bioinformatics/btt469 | DOI Listing |
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