Protein Kinase Serine/Threonine Kinase 24 Positively Regulates Interleukin 17-Induced Inflammation by Promoting IKK Complex Activation

Front Immunol. 2018 Apr 30:9:921. doi: 10.3389/fimmu.2018.00921. eCollection 2018.

Abstract

Interleukin 17 (IL-17) is a key inflammatory cytokine that plays a critical role in tissue inflammation and autoimmune diseases. However, its signaling remains poorly understood. In this study, we identified serine/threonine kinase 24 (Stk24) as a positive modulator of IL-17-mediated signaling and inflammation. Stk24 deficiency or knockdown markedly inhibited IL-17-induced phosphorylation of NF-κB and impaired IL-17-induced chemokines and cytokines expression. Stk24 overexpression greatly enhanced IL-17-induced NF-κB activation and expression of chemokines and cytokines in a kinase activity-independent manner. The IL-17-induced inflammatory response was significantly reduced in Stk24-deficient mice. In addition, the severity of experimental autoimmune encephalomyelitis was markedly reduced in mice with a deficiency of Stk24 in non-hematopoietic cells. We further demonstrated that Stk24 directly interacts with TAK1 and IKKβ and promotes the formation of TAK1/IKK complexes, leading to enhanced IKKβ/NF-κB activation and downstream cytokines and chemokines induction. Collectively, our findings suggest that Stk24 plays an important role in controlling IL-17-triggered inflammation and autoimmune diseases and provides new insight into the therapeutic targets of IL-17-mediated inflammatory disease.

Keywords: IKK; experimental autoimmune encephalomyelitis; inflammation; interleukin 17; serine/threonine kinase 24.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cytokines / immunology
  • Encephalomyelitis, Autoimmune, Experimental / genetics
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • I-kappa B Kinase / genetics*
  • Inflammation / immunology*
  • Interleukin-17 / genetics
  • Interleukin-17 / immunology*
  • MAP Kinase Kinase Kinases / metabolism
  • Mice
  • Mice, Knockout
  • NF-kappa B / metabolism
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics*
  • Signal Transduction*

Substances

  • Cytokines
  • Interleukin-17
  • NF-kappa B
  • Stk24 protein, mouse
  • Protein Serine-Threonine Kinases
  • I-kappa B Kinase
  • MAP Kinase Kinase Kinases
  • MAP kinase kinase kinase 7