The Troyer syndrome protein spartin mediates selective autophagy of lipid droplets.


Journal

Nature cell biology
ISSN: 1476-4679
Titre abrégé: Nat Cell Biol
Pays: England
ID NLM: 100890575

Informations de publication

Date de publication:
08 2023
Historique:
received: 21 03 2022
accepted: 30 05 2023
medline: 14 8 2023
pubmed: 14 7 2023
entrez: 13 7 2023
Statut: ppublish

Résumé

Lipid droplets (LDs) are crucial organelles for energy storage and lipid homeostasis. Autophagy of LDs is an important pathway for their catabolism, but the molecular mechanisms mediating LD degradation by selective autophagy (lipophagy) are unknown. Here we identify spartin as a receptor localizing to LDs and interacting with core autophagy machinery, and we show that spartin is required to deliver LDs to lysosomes for triglyceride mobilization. Mutations in SPART (encoding spartin) lead to Troyer syndrome, a form of complex hereditary spastic paraplegia

Identifiants

pubmed: 37443287
doi: 10.1038/s41556-023-01178-w
pii: 10.1038/s41556-023-01178-w
pmc: PMC10415183
doi:

Substances chimiques

Cell Cycle Proteins 0
Carrier Proteins 0
Triglycerides 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1101-1110

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM097194
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM124348
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG068423
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2023. The Author(s).

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Auteurs

Jeeyun Chung (J)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.

Joongkyu Park (J)

Department of Pharmacology, Department of Neurology, Wayne State University School of Medicine, Detroit, MI, USA.

Zon Weng Lai (ZW)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, MA, USA.

Talley J Lambert (TJ)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Department of Systems Biology, Harvard Medical School, Boston, MA, USA.

Ruth C Richards (RC)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, MA, USA.

Jiuchun Zhang (J)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Tobias C Walther (TC)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA. twalther@mskcc.org.
Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, MA, USA. twalther@mskcc.org.
Broad Institute of Harvard and MIT, Cambridge, MA, USA. twalther@mskcc.org.
Howard Hughes Medical Institute, Boston, MA, USA. twalther@mskcc.org.
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA. twalther@mskcc.org.

Robert V Farese (RV)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA. rfarese@mskcc.org.
Department of Molecular Metabolism, Harvard T. H. Chan School of Public Health, Boston, MA, USA. rfarese@mskcc.org.
Broad Institute of Harvard and MIT, Cambridge, MA, USA. rfarese@mskcc.org.
Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA. rfarese@mskcc.org.

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