Regulated proteolysis as an element of ER stress and autophagy: Implications for intestinal inflammation

Biochim Biophys Acta Mol Cell Res. 2017 Nov;1864(11 Pt B):2183-2190. doi: 10.1016/j.bbamcr.2017.07.008. Epub 2017 Jul 21.

Abstract

Endoplasmic reticulum (ER) stress and autophagy are tightly controlled cellular processes, which are responsible for maintaining protein homeostasis in a cell. Impairment of the interlinking pathways have been implicated in a number of human diseases, prominently in inflammatory bowel disease, where genetic variants in several independent autophagy and ER stress related loci have been associated to increased disease risk. Autophagy is a selective quality control process, which governs the integrity of the cell by removal of aged organelles and proteins via the lysosome, but recently has been shown to actively license the outcome of other signaling pathways by guiding the proteolytic removal of signaling protein complexes (adaptophagy). In this review, we summarize our knowledge on regulated proteolytic events involved in ER stress responses and autophagy, their interplay and potential regulatory effects with a particular focus on intestinal inflammation. This article is part of a Special Issue entitled: Proteolysis as a Regulatory Event in Pathophysiology edited by Stefan Rose-John.

Keywords: Autophagy; Cell death; Er stress; Inflammatory bowel disease; Necroptosis; Proteasome; Proteolysis.

Publication types

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

MeSH terms

  • Autophagy / genetics*
  • Endoplasmic Reticulum Stress / genetics*
  • Humans
  • Inflammatory Bowel Diseases / genetics*
  • Inflammatory Bowel Diseases / pathology
  • Intestinal Mucosa / metabolism
  • Intestines / pathology
  • Lysosomes / metabolism
  • Proteolysis*
  • Signal Transduction