The different autophagy degradation pathways and neurodegeneration

Copyright © 2022 Elsevier Inc. All rights reserved..

The term autophagy encompasses different pathways that route cytoplasmic material to lysosomes for degradation and includes macroautophagy, chaperone-mediated autophagy, and microautophagy. Since these pathways are crucial for degradation of aggregate-prone proteins and dysfunctional organelles such as mitochondria, they help to maintain cellular homeostasis. As post-mitotic neurons cannot dilute unwanted protein and organelle accumulation by cell division, the nervous system is particularly dependent on autophagic pathways. This dependence may be a vulnerability as people age and these processes become less effective in the brain. Here, we will review how the different autophagic pathways may protect against neurodegeneration, giving examples of both polygenic and monogenic diseases. We have considered how autophagy may have roles in normal CNS functions and the relationships between these degradative pathways and different types of programmed cell death. Finally, we will provide an overview of recently described strategies for upregulating autophagic pathways for therapeutic purposes.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:110

Enthalten in:

Neuron - 110(2022), 6 vom: 16. März, Seite 935-966

Sprache:

Englisch

Beteiligte Personen:

Fleming, Angeleen [VerfasserIn]
Bourdenx, Mathieu [VerfasserIn]
Fujimaki, Motoki [VerfasserIn]
Karabiyik, Cansu [VerfasserIn]
Krause, Gregory J [VerfasserIn]
Lopez, Ana [VerfasserIn]
Martín-Segura, Adrián [VerfasserIn]
Puri, Claudia [VerfasserIn]
Scrivo, Aurora [VerfasserIn]
Skidmore, John [VerfasserIn]
Son, Sung Min [VerfasserIn]
Stamatakou, Eleanna [VerfasserIn]
Wrobel, Lidia [VerfasserIn]
Zhu, Ye [VerfasserIn]
Cuervo, Ana Maria [VerfasserIn]
Rubinsztein, David C [VerfasserIn]

Links:

Volltext

Themen:

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

Anmerkungen:

Date Completed 05.04.2022

Date Revised 17.03.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.neuron.2022.01.017

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM336667116