Stressed out about obesity: IRE1α-XBP1 in metabolic disorders

Trends Endocrinol Metab. 2011 Sep;22(9):374-81. doi: 10.1016/j.tem.2011.05.002. Epub 2011 Jun 22.

Abstract

The global obesity epidemic is associated with a series of health-threatening diseases including type 2 diabetes. Accumulating evidence suggest that the physiology and homeostasis of the endoplasmic reticulum (ER) is intimately involved in the underlying mechanisms linking obesity and diabetes. Specifically, recent studies indicate a crucial role for the inositol-requiring enzyme 1α (IRE1α)/X-box binding protein 1 (XBP1) pathway, the most conserved branch of the unfolded protein response (UPR), in glucose and lipid metabolism as well as in insulin function. Focusing on the IRE1α-XBP1 pathway, we review recent advances in our understanding of the role of UPR in obesity and obesity-associated metabolic disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • DNA-Binding Proteins / metabolism*
  • Diabetes Mellitus, Type 2 / metabolism
  • Endoplasmic Reticulum / metabolism*
  • Endoribonucleases / metabolism*
  • Insulin Resistance
  • Mice
  • Obesity / metabolism*
  • Protein Serine-Threonine Kinases / metabolism*
  • Regulatory Factor X Transcription Factors
  • Transcription Factors / metabolism*
  • Unfolded Protein Response
  • X-Box Binding Protein 1

Substances

  • DNA-Binding Proteins
  • Regulatory Factor X Transcription Factors
  • Transcription Factors
  • X-Box Binding Protein 1
  • Xbp1 protein, mouse
  • Ern1 protein, mouse
  • Protein Serine-Threonine Kinases
  • Endoribonucleases