S1P d20:1, an endogenous modulator of S1P d18:1/S1P


Journal

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
ISSN: 1530-6860
Titre abrégé: FASEB J
Pays: United States
ID NLM: 8804484

Informations de publication

Date de publication:
03 2020
Historique:
received: 24 09 2019
revised: 27 12 2019
accepted: 27 12 2019
pubmed: 17 1 2020
medline: 26 1 2021
entrez: 17 1 2020
Statut: ppublish

Résumé

Sphingosine 1-phosphate (S1P) signaling influences numerous cell biological mechanisms such as differentiation, proliferation, survival, migration, and angiogenesis. Intriguingly, our current knowledge is based solely on the role of S1P with an 18-carbon long-chain base length, S1P d18:1. Depending on the composition of the first and rate-limiting enzyme of the sphingolipid de novo metabolism, the serine palmitoyltransferase, other chain lengths have been described in vivo. While cells are also able to produce S1P d20:1, its abundance and function remains elusive so far. Our experiments are highlighting the role of S1P d20:1 in the mouse central nervous system (CNS) and human glioblastoma. We show here that S1P d20:1 and its precursors are detectable in both healthy mouse CNS-tissue and human glioblastoma. On the functional level, we focused our work on one particular, well-characterized pathway, the induction of cyclooxygenase (COX)-2 expression via the S1P receptor 2 (S1P

Identifiants

pubmed: 31944406
doi: 10.1096/fj.201902391R
doi:

Substances chimiques

Lysophospholipids 0
Sphingosine-1-Phosphate Receptors 0
sphingosine 1-phosphate 26993-30-6
Ptgs2 protein, mouse EC 1.14.99.-
Cyclooxygenase 2 EC 1.14.99.1
Sphingosine NGZ37HRE42

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3932-3942

Informations de copyright

© 2020 The Authors. The FASEB Journal published by Wiley Periodicals, Inc. on behalf of Federation of American Societies for Experimental Biology.

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Auteurs

Rajkumar Vutukuri (R)

Institute of General Pharmacology and Toxicology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Alexander Koch (A)

Institute of General Pharmacology and Toxicology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Sandra Trautmann (S)

Institute of Clinical Pharmacology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Yannick Schreiber (Y)

Fraunhofer Institute of Molecular Biology and Applied Ecology-Project Group Translational Medicine and Pharmacology (IME-TMP), Frankfurt am Main, Germany.

Dominique Thomas (D)

Institute of Clinical Pharmacology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Franziska Mayser (F)

Department of Neurology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Dagmar Meyer Zu Heringdorf (D)

Institute of General Pharmacology and Toxicology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Josef Pfeilschifter (J)

Institute of General Pharmacology and Toxicology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Waltraud Pfeilschifter (W)

Department of Neurology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

Robert Brunkhorst (R)

Department of Neurology, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.

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