Emerging roles of the γ-secretase-notch axis in inflammation

Pharmacol Ther. 2015 Mar:147:80-90. doi: 10.1016/j.pharmthera.2014.11.005. Epub 2014 Nov 8.

Abstract

γ-Secretase is a distinct proteolytic complex required for the activation of many transmembrane proteins. The cleavage of substrates by γ-secretase plays diverse biological roles in producing essential products for the organism. More than 90 transmembrane proteins have been reported to be substrates of γ-secretase. Two of the most widely known and studied of these substrates are the amyloid precursor protein (APP) and the Notch receptor, which are precursors for the generation of amyloid-β (Aβ) and the Notch intracellular domain (NICD), respectively. The wide spectrum of γ-secretase substrates has made analyses of the pathology of γ-secretase-related diseases and underlying mechanisms challenging. Inflammation is an important aspect of disease pathology that requires an in-depth analysis. γ-Secretase may contribute to disease development or progression by directly increasing and regulating production of pro-inflammatory cytokines. This review summarizes recent evidence for a role of γ-secretase in inflammatory diseases, and discusses the potential use of γ-secretase inhibitors as an effective future treatment option.

Keywords: Inflammation; Inflammatory diseases; Notch; Stroke; γ-Secretase.

Publication types

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

MeSH terms

  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / metabolism
  • Amyloid Precursor Protein Secretases / antagonists & inhibitors
  • Amyloid Precursor Protein Secretases / physiology*
  • Animals
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / metabolism*
  • Receptors, Notch / antagonists & inhibitors
  • Receptors, Notch / physiology*
  • Stroke / drug therapy
  • Stroke / metabolism

Substances

  • Enzyme Inhibitors
  • Receptors, Notch
  • Amyloid Precursor Protein Secretases