ER stress signaling and neurodegeneration: At the intersection between Alzheimer's disease and Prion-related disorders

Mauricio Torres, José Manuel Matamala, Claudia Duran-Aniotz, Victor Hugo Cornejo, Andrew Foley, Claudio Hetz

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

Alzheimer's and Prion diseases are two neurodegenerative conditions sharing different pathophysiological characteristics. Disease symptoms are associated with the abnormal accumulation of protein aggregates, which are generated by the misfolding and oligomerization of specific proteins. Recent functional studies uncovered a key role of endoplasmic reticulum (ER) stress and the unfolded protein response (UPR) in the occurrence of synaptic dysfunction and neurodegeneration in Prion-related disorders and Alzheimer's disease. Here we review common pathological features of both diseases, emphasizing the link between amyloid formation, its pathogenesis and alterations in ER proteostasis. The potential benefits of targeting the UPR as a therapeutic strategy is also discussed.

Original languageEnglish
Pages (from-to)69-75
Number of pages7
JournalVirus Research
Volume207
DOIs
StatePublished - 2 Sep 2015

Keywords

  • Amyloid formation
  • ER-stress
  • Prion-like diseases
  • Sustained translational repression
  • Targeting ER-stress
  • Unfolded protein response (UPR)

Fingerprint

Dive into the research topics of 'ER stress signaling and neurodegeneration: At the intersection between Alzheimer's disease and Prion-related disorders'. Together they form a unique fingerprint.

Cite this