Cell-intrinsic ceramides determine T cell function during melanoma progression.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
25 11 2022
Historique:
received: 31 08 2022
accepted: 15 11 2022
entrez: 25 11 2022
pubmed: 26 11 2022
medline: 29 11 2022
Statut: epublish

Résumé

Acid sphingomyelinase (Asm) and acid ceramidase (Ac) are parts of the sphingolipid metabolism. Asm hydrolyzes sphingomyelin to ceramide, which is further metabolized to sphingosine by Ac. Ceramide generates ceramide-enriched platforms that are involved in receptor clustering within cellular membranes. However, the impact of cell-intrinsic ceramide on T cell function is not well characterized. By using T cell-specific Asm- or Ac-deficient mice, with reduced or elevated ceramide levels in T cells, we identified ceramide to play a crucial role in T cell function in vitro and in vivo. T cell-specific ablation of Asm in

Identifiants

pubmed: 36426850
doi: 10.7554/eLife.83073
pii: 83073
pmc: PMC9699697
doi:
pii:

Substances chimiques

Ceramides 0
Sphingosine NGZ37HRE42
Receptors, Antigen, T-Cell 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

© 2022, Hose, Günther et al.

Déclaration de conflit d'intérêts

MH, AG, EN, FS, TS, JF, AP, BK, KB, EG, AH, JB, AW, WH No competing interests declared

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Auteurs

Matthias Hose (M)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Anne Günther (A)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Eyad Naser (E)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Fabian Schumacher (F)

Institute of Pharmacy, Freie Universität Berlin, Berlin, Germany.

Tina Schönberger (T)

Institute of Physiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Julia Falkenstein (J)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Athanasios Papadamakis (A)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Burkhard Kleuser (B)

Institute of Pharmacy, Freie Universität Berlin, Berlin, Germany.

Katrin Anne Becker (KA)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Erich Gulbins (E)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Adriana Haimovitz-Friedman (A)

Memorial Sloan Kettering Cancer Center, New York City, United States.

Jan Buer (J)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Astrid M Westendorf (AM)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Wiebke Hansen (W)

Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

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Classifications MeSH