Polyglutamine expansion disturbs the endoplasmic reticulum formation, leading to caspase-7 activation through Bax

Biochem Biophys Res Commun. 2014 Jan 24;443(4):1232-8. doi: 10.1016/j.bbrc.2013.12.114. Epub 2014 Jan 2.

Abstract

The endoplasmic reticulum (ER) plays a pivotal role in cellular functions such as the ER stress response. However, the effect of the ER membrane on caspase activation remains unclear. This study reveals that polyglutamine oligomers augmented at ER induce insertion of Bax into the ER membrane, thereby activating caspase-7. In line with the role of ER in cell death induced by polyglutamine expansion, the ER membrane was found to be disrupted and dilated in the brain of a murine model of Huntington's disease. We can conclude that polyglutamine expansion may drive caspase-7 activation by disrupting the ER membrane.

Keywords: Apoptosis; Bcl-2 family; Caspase; Endoplasmic reticulum; Neurodegeneration; Polyglutamine expansion disorder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Brain / metabolism
  • Brain / pathology
  • Caspase 7 / metabolism*
  • Disease Models, Animal
  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum / pathology
  • Enzyme Activation
  • HEK293 Cells
  • Humans
  • Huntingtin Protein
  • Huntington Disease / genetics
  • Huntington Disease / metabolism*
  • Huntington Disease / pathology
  • Intracellular Membranes / metabolism
  • Intracellular Membranes / pathology
  • Mice
  • Mice, Transgenic
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Peptides / metabolism*
  • bcl-2-Associated X Protein / metabolism*

Substances

  • Bax protein, mouse
  • Htt protein, mouse
  • Huntingtin Protein
  • Nerve Tissue Proteins
  • Nuclear Proteins
  • Peptides
  • bcl-2-Associated X Protein
  • polyglutamine
  • Casp7 protein, mouse
  • Caspase 7