| First Author | Kim Y | Year | 2019 |
| Journal | Infect Immun | Volume | 87 |
| Issue | 8 | PubMed ID | 31160364 |
| Mgi Jnum | J:289426 | Mgi Id | MGI:6435048 |
| Doi | 10.1128/IAI.00132-19 | Citation | Kim Y, et al. (2019) NF-kappaB RelA Is Required for Hepatoprotection during Pneumonia and Sepsis. Infect Immun 87(8) |
| abstractText | Pneumonia and sepsis are distinct but integrally linked public health concerns. The hepatic acute-phase response (APR), which is largely dependent on transcription factors NF-kappaB RelA and STAT3, is a hallmark of these pathologies and other injurious conditions. Inactivation of the APR can promote liver injury, a frequently observed organ dysfunction during sepsis. However, whether or how the acute-phase changes promote liver tissue resilience during infections is unclear. To determine the hepatoprotective role of the hepatic APR, we utilized mice bearing hepatocyte-specific deletions of either RelA or STAT3. Mice were challenged intratracheally (i.t.), intravenously (i.v.), or intraperitoneally (i.p.) with Escherichia coli, Klebsiella pneumoniae, Streptococcus pneumoniae, lipopolysaccharide (LPS), or alpha-galactosylceramide (alphaGalCer) to induce pneumonia, sepsis, or NKT cell activation. Liver injury was observed in RelA-null (hepRelA(Delta/Delta)) mice but not STAT3-null (hepSTAT3(Delta/Delta)) mice during pneumonia. The absence of RelA resulted in hepatotoxicity across several models of pneumonia, sepsis, and NKT cell activation. Injury was associated with increased levels of activated caspase-3 and -8 and substantial alteration of the hepatic transcriptome. Hepatotoxicity in the absence of RelA could be reversed by neutralization of tumor necrosis factor alpha (TNF-alpha). These results indicate the requirement of RelA-dependent inducible hepatoprotection during pneumonia and sepsis. Further, the results demonstrate that RelA-dependent gene programs are critical for maintaining liver homeostasis against TNF-alpha-driven immunotoxicity. |
