RTN3L and CALCOCO1 function in parallel to maintain proteostasis in the endoplasmic reticulum.

Aggregation-prone proteins endoplasmic reticulum endoplasmic reticulum stress reticulophagy receptors selective autophagy

Journal

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

Informations de publication

Date de publication:
31 May 2024
Historique:
medline: 31 5 2024
pubmed: 31 5 2024
entrez: 31 5 2024
Statut: aheadofprint

Résumé

Reticulophagy is mediated by autophagy receptors that function in one of the two domains of the ER, tubules or flat sheets. Three different conserved mammalian receptors mediate autophagy in ER tubules: RTN3L, ATL3 and CALCOCO1. Previous studies have shown that RTN3L maintains proteostasis by targeting mutant aggregation-prone proteins for autophagy at distinct foci in ER tubules that we named ERPHS (

Identifiants

pubmed: 38818751
doi: 10.1080/15548627.2024.2353502
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-9

Auteurs

Kamal Kumar (K)

Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.

Ravi Chidambaram (R)

Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.

Smriti Parashar (S)

Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.

Susan Ferro-Novick (S)

Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.

Classifications MeSH