Sensing endoplasmic reticulum stress

Adv Exp Med Biol. 2012:738:153-68. doi: 10.1007/978-1-4614-1680-7_10.

Abstract

This chapter provides an overview of our present understanding of mechanisms of sensing protein folding status and endoplasmic reticulum (ER) stress in eukaryotic cells. The ER folds and matures most secretory and transmembrane proteins. Mis- or unfolded proteins are sensed by specialized ER stress sensors, such as IRE1, PERK and ATF6, which initiate several cellular responses and signaling pathways to restore ER homeostasis. These intracellular signaling events are called the unfolded protein response (UPR). Here we focus on how ER stress and protein folding status in the ER are sensed by the ER stress sensors by summarizing results from recent structural, biochemical and genetic approaches.

Publication types

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

MeSH terms

  • Activating Transcription Factor 6 / genetics
  • Activating Transcription Factor 6 / immunology
  • Animals
  • Endoplasmic Reticulum / genetics
  • Endoplasmic Reticulum / immunology*
  • Endoplasmic Reticulum Stress / genetics
  • Endoplasmic Reticulum Stress / immunology*
  • Endoribonucleases / genetics
  • Endoribonucleases / immunology
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / immunology
  • Protein Folding*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / immunology
  • Unfolded Protein Response / genetics
  • Unfolded Protein Response / immunology*
  • eIF-2 Kinase / genetics
  • eIF-2 Kinase / immunology

Substances

  • ATF6 protein, human
  • Activating Transcription Factor 6
  • Membrane Proteins
  • ERN2 protein, human
  • PERK kinase
  • Protein Serine-Threonine Kinases
  • eIF-2 Kinase
  • Endoribonucleases