Evidence map›Paper›PMID 36142188›Full record

ReviewInternational journal of molecular sciences2022

Platelet-Derived S1P and Its Relevance for the Communication with Immune Cells in Multiple Human Diseases.

Céline Tolksdorf, Eileen Moritz, Robert Wolf, Ulrike Meyer, Sascha Marx, Sandra Bien-Möller, Ulrike Garscha, Gabriele Jedlitschky, Bernhard H Rauch

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Céline TolksdorfDivision of Pharmacology and Toxicology, School of Medicine and Health Sciences, Carl von Ossietzky University Oldenburg, 26129 Oldenburg, Germany.ORCID 0000-0002-0925-6745
Eileen MoritzDepartment of General Pharmacology, University Medicine Greifswald, 17489 Greifswald, Germany.
Robert WolfDepartment of General Pharmacology, University Medicine Greifswald, 17489 Greifswald, Germany.
Ulrike MeyerDivision of Pharmacology and Toxicology, School of Medicine and Health Sciences, Carl von Ossietzky University Oldenburg, 26129 Oldenburg, Germany.
Sascha MarxDepartment of Neurosurgery, University Medicine Greifswald, 17489 Greifswald, Germany.ORCID 0000-0002-6451-5404
Sandra Bien-MöllerDepartment of General Pharmacology, University Medicine Greifswald, 17489 Greifswald, Germany.ORCID 0000-0002-0603-8953
Ulrike GarschaInstitute of Pharmacy, University of Greifswald, 17489 Greifswald, Germany.ORCID 0000-0002-3645-7833
Gabriele JedlitschkyDepartment of General Pharmacology, University Medicine Greifswald, 17489 Greifswald, Germany.
Bernhard H RauchDivision of Pharmacology and Toxicology, School of Medicine and Health Sciences, Carl von Ossietzky University Oldenburg, 26129 Oldenburg, Germany.ORCID 0000-0002-6003-4662
Universitätsmedizin Greifswald · DECarl von Ossietzky Universität Oldenburg · DEUniversität Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingosine-1-phosphate (S1P) is a versatile signaling lipid involved in the regulation of numerous cellular processes. S1P regulates cellular proliferation, migration, and apoptosis as well as the function of immune cells. S1P is generated from sphingosine (Sph), which derives from the ceramide metabolism. In particular, high concentrations of S1P are present in the blood. This originates mainly from erythrocytes, endothelial cells (ECs), and platelets. While erythrocytes function as a storage pool for circulating S1P, platelets can rapidly generate S1P de novo, store it in large quantities, and release it when the platelet is activated. Platelets can thus provide S1P in a short time when needed or in the case of an injury with subsequent platelet activation and thereby regulate local cellular responses. In addition, platelet-dependently generated and released S1P may also influence long-term immune cell functions in various disease processes, such as inflammation-driven vascular diseases. In this review, the metabolism and release of platelet S1P are presented, and the autocrine versus paracrine functions of platelet-derived S1P and its relevance in various disease processes are discussed. New pharmacological approaches that target the auto- or paracrine effects of S1P may be therapeutically helpful in the future for pathological processes involving S1P.

Indexed as

Blood PlateletsSphingosineCell CommunicationCeramidesEndothelial CellsHumansLysophospholipidsCeramidesLysophospholipidsSphingosinesphingosine 1-phosphateimmune cellsplateletsS1PS1P receptorssphingosine-1-phosphate

Identifiers

PMID36142188
PMCPMC9499465
OpenAlexW4295011758

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.