Mutual regulation of metabolic processes and proinflammatory NF-κB signaling

J Allergy Clin Immunol. 2020 Oct;146(4):694-705. doi: 10.1016/j.jaci.2020.07.027. Epub 2020 Aug 6.

Abstract

The nuclear factor kappa B (NF-κB) signaling system, a key regulator of immunologic processes, also affects a plethora of metabolic changes associated with inflammation and the immune response. NF-κB-regulating signaling cascades, in concert with NF-κB-mediated transcriptional events, control the metabolism at several levels. NF-κB modulates apical components of metabolic processes including metabolic hormones such as insulin and glucagon, the cellular master switches 5' AMP-activated protein kinase and mTOR, and also numerous metabolic enzymes and their respective regulators. Vice versa, metabolic enzymes and their products also exert multilevel control of NF-κB activity, thereby creating a highly connected regulatory network. These insights have resulted in the identification of the noncanonical IκB kinase kinases IκB kinase ɛ and TBK1, which are upregulated by overnutrition, and may therefore be suitable potential therapeutic targets for metabolic syndromes. An inhibitor interfering with the activity of both kinases reduces obesity-related metabolic dysfunctions in mouse models and the encouraging results from a recent clinical trial indicate that targeting these NF-κB pathway components improves glucose homeostasis in a subset of patients with type 2 diabetes.

Keywords: NF-κB; cancer; inflammation; metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Carrier Proteins / metabolism
  • Cyclic AMP / metabolism
  • Diabetes Mellitus, Type 2 / etiology
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / therapy
  • Disease Management
  • Disease Susceptibility
  • Energy Metabolism*
  • Glucagon / metabolism
  • Humans
  • I-kappa B Kinase / metabolism
  • Inflammation / etiology
  • Inflammation / metabolism
  • Insulin / metabolism
  • Mitochondria / metabolism
  • Molecular Targeted Therapy
  • NF-kappa B / metabolism*
  • Protein Binding
  • Signal Transduction*
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Biomarkers
  • Carrier Proteins
  • Insulin
  • NF-kappa B
  • Glucagon
  • Cyclic AMP
  • TOR Serine-Threonine Kinases
  • I-kappa B Kinase