SREBP-1c overactivates ROS-mediated hepatic NF-κB inflammatory pathway in dairy cows with fatty liver

Cell Signal. 2015 Oct;27(10):2099-109. doi: 10.1016/j.cellsig.2015.07.011. Epub 2015 Jul 17.

Abstract

Dairy cows with fatty liver are characterized by hepatic lipid accumulation and a severe inflammatory response. Sterol receptor element binding protein-1c (SREBP-1c) and nuclear factor κB (NF-κB) are components of the main pathways for controlling triglyceride (TG) accumulation and inflammatory levels, respectively. A previous study demonstrated that hepatic inflammatory levels are positively correlated with hepatic TG content. We therefore speculated that SREBP-1c might play an important role in the overactivation of the hepatic NF-κB inflammatory pathway in cows with fatty liver. Compared with healthy cows, cows with fatty liver exhibited severe hepatic injury and high blood concentrations of the inflammatory cytokines TNF-α, IL-6 and IL-1β. Hepatic SREBP-1c-mediated lipid synthesis and the NF-κB inflammatory pathway were both overinduced in cows with fatty liver. In vitro, treatment with non-esterified fatty acids (NEFA) further increased SREBP-1c expression and NF-κB pathway activation, which then promoted TG and inflammatory cytokine synthesis. SREBP-1c overexpression overactivated the NF-κB inflammatory pathway in hepatocytes by increasing ROS content and not through TLR4. Furthermore, SREBP-1c silencing decreased ROS content and further attenuated the activation of the NEFA-induced NF-κB pathway, thereby decreasing TNF-α, IL-6 and IL-1β synthesis. SREBP-1c-overexpressing mice exhibited hepatic steatosis and an overinduced hepatic NF-κB pathway. Taken together, these results indicate that SREBP-1c enhances the NEFA-induced overactivation of the NF-κB inflammatory pathway by increasing ROS in cow hepatocytes, thereby further increasing hepatic inflammatory injury in cows with fatty liver.

Keywords: Dairy cows; Fatty liver; Non-esterified fatty acids; Nuclear factor κB; Sterol receptor element binding protein-1c.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cattle Diseases / immunology
  • Cattle Diseases / metabolism*
  • Cells, Cultured
  • Fatty Liver / immunology
  • Fatty Liver / metabolism
  • Fatty Liver / veterinary*
  • Female
  • Hepatocytes / immunology
  • Hepatocytes / metabolism
  • Liver / immunology
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mice
  • Reactive Oxygen Species / metabolism*
  • Sterol Regulatory Element Binding Protein 1 / physiology*
  • Toll-Like Receptor 4 / metabolism
  • Transcription Factor RelA / metabolism*

Substances

  • Reactive Oxygen Species
  • Sterol Regulatory Element Binding Protein 1
  • Toll-Like Receptor 4
  • Transcription Factor RelA