Lysosomal enzyme trafficking : from molecular mechanisms to human diseases

Copyright © 2023 Elsevier Ltd. All rights reserved..

Lysosomes degrade and recycle macromolecules that are delivered through the biosynthetic, endocytic, and autophagic routes. Hydrolysis of the different classes of macromolecules is catalyzed by about 70 soluble enzymes that are transported from the Golgi apparatus to lysosomes in a mannose 6-phosphate (M6P)-dependent process. The molecular machinery that generates M6P tags for receptor-mediated targeting of lysosomal enzymes was thought to be understood in detail. However, recent studies on the M6P pathway have identified a previously uncharacterized core component, yielded structural insights in known components, and uncovered functions in various human diseases. Here we review molecular mechanisms of lysosomal enzyme trafficking and discuss its relevance for rare lysosomal disorders, cancer, and viral infection.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:34

Enthalten in:

Trends in cell biology - 34(2024), 3 vom: 19. März, Seite 198-210

Sprache:

Englisch

Beteiligte Personen:

Braulke, Thomas [VerfasserIn]
Carette, Jan E [VerfasserIn]
Palm, Wilhelm [VerfasserIn]

Links:

Volltext

Themen:

Cancer metabolism
Carrier Proteins
Journal Article
LYSET
Lysosomal enzymes
Lysosomal storage disorders
Mannose 6-phosphate pathway
Review
Viral infections

Anmerkungen:

Date Completed 11.03.2024

Date Revised 14.03.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.tcb.2023.06.005

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM359748082