Regulation of Fn14 stability by SCFFbxw7α during septic acute kidney injury

Am J Physiol Renal Physiol. 2019 Jun 1;316(6):F1273-F1281. doi: 10.1152/ajprenal.00627.2018. Epub 2019 Apr 24.

Abstract

Acute kidney injury (AKI) initiated by sepsis remains a thorny problem despite recent advancements in its clinical management. Having been found to be activated during AKI, fibroblast growth factor-inducible molecule 14 (Fn14) may be a potential therapeutic target because of its involvement in the molecular basis of injury. Here, we report that LPS induces apoptosis of mouse cortical tubule cells mediated by Fn14, for which simultaneous Toll-like receptor (TLR)4 activation is required. Mechanistically, TLR4 activation by lipopolysaccharide, through disassociating E3 ligase SCFFbxw7α from Fn14, dismantles Lys48-linked polyubiquitination of Fn14 and stabilizes it. Pharmacological deactivation of Fn14 with monoclonal antibody ITEM-2 provides effective protection against lethal sepsis and AKI in mice. Our study underscores an adaptive mechanism whereby TLR4 regulates SCFFbxw7α-dependent Fn14 stabilization during inflammatory tubular damage and further supports investigation of targeting Fn14 in clinical trials of patients with septic AKI.

Keywords: SCF; acute kidney injury; fibroblast growth factor-inducible molecule 14; sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / genetics
  • Acute Kidney Injury / metabolism*
  • Acute Kidney Injury / microbiology
  • Acute Kidney Injury / pathology
  • Animals
  • Apoptosis
  • Disease Models, Animal
  • F-Box-WD Repeat-Containing Protein 7 / genetics
  • F-Box-WD Repeat-Containing Protein 7 / metabolism*
  • Kidney Tubules / metabolism*
  • Kidney Tubules / microbiology
  • Kidney Tubules / pathology
  • Macrophages / metabolism*
  • Macrophages / microbiology
  • Macrophages / pathology
  • Mice
  • Mice, Inbred C57BL
  • Protein Stability
  • RAW 264.7 Cells
  • Sepsis / complications*
  • Sepsis / microbiology
  • Signal Transduction
  • TWEAK Receptor / genetics
  • TWEAK Receptor / metabolism*
  • Toll-Like Receptor 4 / metabolism

Substances

  • F-Box-WD Repeat-Containing Protein 7
  • Fbxw7 protein, mouse
  • TWEAK Receptor
  • Tlr4 protein, mouse
  • Tnfrsf12a protein, mouse
  • Toll-Like Receptor 4