TRAIL receptor deletion in mice suppresses the inflammation of nutrient excess

Leila Idrissova, Harmeet Malhi, Nathan W. Werneburg, Nathan K. Lebrasseur, Steven F. Bronk, Christian Fingas, Tamar Tchkonia, Tamar Pirtskhalava, Thomas A. White, Michael B. Stout, Petra Hirsova, Anuradha Krishnan, Christian Liedtke, Christian Trautwein, Niklas Finnberg, Wafik S. El-Deiry, James L. Kirkland, Gregory J. Gores

Research output: Contribution to journalArticlepeer-review

50 Scopus citations


Background & Aims Low-grade chronic inflammation is a cardinal feature of the metabolic syndrome, yet its pathogenesis is not well defined. The purpose of this study was to examine the role of TRAIL receptor (TR) signaling in the pathogenesis of obesity-associated inflammation using mice with the genetic deletion of TR. Methods TR knockout (TR-/-) mice and their littermate wild-type (WT) mice were fed a diet high in saturated fat, cholesterol and fructose (FFC) or chow. Metabolic phenotyping, liver injury, and liver and adipose tissue inflammation were assessed. Chemotaxis and activation of mouse bone marrow-derived macrophages (BMDMo) was measured. Results Genetic deletion of TR completely repressed weight gain, adiposity and insulin resistance in FFC-fed mice. Moreover, TR-/- mice suppressed steatohepatitis, with essentially normal serum ALT, hepatocyte apoptosis and liver triglyceride accumulation. Gene array data implicated inhibition of macrophage-associated hepatic inflammation in the absence of the TR. In keeping with this, there was diminished accumulation and activation of inflammatory macrophages in liver and adipose tissue. TR-/- BMDMO manifest reduced chemotaxis and diminished activation of nuclear factor-κ B signaling upon activation by palmitate and lipopolysaccharide. Conclusions These data advance the concept that macrophage-associated hepatic and adipose tissue inflammation of nutrient excess requires TR signaling.

Original languageEnglish (US)
Pages (from-to)1156-1163
Number of pages8
JournalJournal of hepatology
Issue number5
StatePublished - May 1 2015

ASJC Scopus subject areas

  • Hepatology


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