A conserved requirement for RME-8/DNAJC13 in neuronal autophagic lysosome reformation.

Autophagy clathrin endocytosis lysosomes neurodegeneration trafficking

Journal

Autophagy
ISSN: 1554-8635
Titre abrégé: Autophagy
Pays: United States
ID NLM: 101265188

Informations de publication

Date de publication:
09 Nov 2023
Historique:
medline: 9 11 2023
pubmed: 9 11 2023
entrez: 9 11 2023
Statut: aheadofprint

Résumé

Autophagosomes fuse with lysosomes, forming autolysosomes that degrade engulfed cargo. To maintain lysosomal capacity, autophagic lysosome reformation (ALR) must regenerate lysosomes from autolysosomes using a membrane tubule-based process. Maintaining lysosomal capacity is required to maintain cellular health, especially in neurons where lysosomal dysfunction has been repeatedly implicated in neurodegenerative disease. The DNA-J domain HSC70 co-chaperone RME-8/DNAJC13 has been linked to endosomal coat protein regulation and to neurological disease. We report new analysis of the requirements for the RME-8/DNAJC13 protein in neurons, focusing on intact

Identifiants

pubmed: 37942902
doi: 10.1080/15548627.2023.2269028
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-17

Commentaires et corrections

Type : UpdateOf

Auteurs

Sierra B Swords (SB)

Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.

Nuo Jia (N)

Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, USA.

Anne Norris (A)

Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.

Jil Modi (J)

Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.

Qian Cai (Q)

Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, USA.

Barth D Grant (BD)

Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.
Center for Lipid Research, New Brunswick, NJ, USA.

Classifications MeSH