The role of protein clearance mechanisms in organismal ageing and age-related diseases

Proteins are subject to continuous and complex quality-control mechanisms, which ensure integrity of the proteome. Vilchez et al. review how a demise in these processes, collectively referred to as proteostasis, is linked to organismal ageing and the development of age-associated diseases. The abili...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature communications Jg. 5; H. 1; S. 5659
Hauptverfasser: Vilchez, David, Saez, Isabel, Dillin, Andrew
Format: Journal Article
Sprache:Englisch
Veröffentlicht: London Nature Publishing Group UK 08.12.2014
Nature Publishing Group
Schlagworte:
ISSN:2041-1723, 2041-1723
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Proteins are subject to continuous and complex quality-control mechanisms, which ensure integrity of the proteome. Vilchez et al. review how a demise in these processes, collectively referred to as proteostasis, is linked to organismal ageing and the development of age-associated diseases. The ability to maintain a functional proteome, or proteostasis, declines during the ageing process. Damaged and misfolded proteins accumulate with age, impairing cell function and tissue homeostasis. The accumulation of damaged proteins contributes to multiple age-related diseases such as Alzheimer’s, Parkinson’s or Huntington’s disease. Damaged proteins are degraded by the ubiquitin–proteasome system or through autophagy-lysosome, key components of the proteostasis network. Modulation of either proteasome activity or autophagic-lysosomal potential extends lifespan and protects organisms from symptoms associated with proteostasis disorders, suggesting that protein clearance mechanisms are directly linked to ageing and age-associated diseases.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
content type line 14
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms6659