SIGMAR1/Sigma-1 Receptor: A Key Regulator in Stabilizing and Translating

ATG8 LC3 SIGMAR1 autophagy lipidation localized translation

Journal

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

Informations de publication

Date de publication:
06 Oct 2024
Historique:
medline: 6 10 2024
pubmed: 6 10 2024
entrez: 6 10 2024
Statut: aheadofprint

Résumé

Macroautophagy/autophagy degrades and recycles cellular constituents via the lysosome to maintain cellular homeostasis. Our study identified the endoplasmic reticulum (ER)-resident SIGMAR1 (sigma non-opioid intracellular receptor 1) as a critical regulator of the biosynthesis of Atg8-family proteins that leads to the lipidation that is essential during autophagosome formation. We demonstrate that SIGMAR1 stabilizes

Identifiants

pubmed: 39369298
doi: 10.1080/15548627.2024.2413313
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Yu-Jie Chen (YJ)

Department of Cell & Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.

Jeffrey Knupp (J)

Department of Cell & Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Cellular and Molecular Biology Program, University of Michigan Medical School, Ann Arbor, MI, USA.

Emily Wang (E)

Department of Cell & Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.

Peter Arvan (P)

Division of Metabolism Endocrinology & Diabetes, University of Michigan Medical School, Ann Arbor, MI, USA.

Billy Tsai (B)

Department of Cell & Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Cellular and Molecular Biology Program, University of Michigan Medical School, Ann Arbor, MI, USA.

Classifications MeSH