Evidence map›Paper›PMID 27623848›Full record

ArticleJournal of lipid research2016

Cytokine-induced release of ceramide-enriched exosomes as a mediator of cell death signaling in an oligodendroglioma cell line.

Maria Podbielska, Zdzisław M Szulc, Ewa Kurowska, Edward L Hogan, Jacek Bielawski, Alicja Bielawska, Narayan R Bhat

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 70 citations in OpenAlex.

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  16. The role of exosomes from BALF in lung disease.Journal of cellular physiology · 2022
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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

7 authors at 2 institutions in 2 countries.

Maria PodbielskaDepartments of Neuroscience Medical University of South Carolina, Charleston, SC 29425.
Zdzisław M SzulcBiochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425.
Ewa KurowskaLaboratory of Signaling Proteins, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114 Wrocław, Poland.
Edward L HoganDepartments of Neuroscience Medical University of South Carolina, Charleston, SC 29425.
Jacek BielawskiBiochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425.
Alicja BielawskaBiochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425.
Narayan R BhatDepartments of Neuroscience Medical University of South Carolina, Charleston, SC 29425 bhatnr@musc.edu.
Medical University of South Carolina · USLudwik Hirszfeld Institute of Immunology and Experimental Therapy · PL

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
THE ROLE OF LACTOSYLCERAMIDE IN RENAL AGING AND DISEASEP20RR017677 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MAO, CUNGUI · 2002 to 2011
$23.4M
RESEARCH PILOT PROJECTS PROGRAMP30GM103339 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HANNUN, YUSUF AWNI · 2012 to 2016
$5.4M
NCI NIH HHS P30 CA138313NCRR NIH HHS P20 RR017677NIGMS NIH HHS P30 GM103339
6 · The paper itself

Abstract

Th1 pro-inflammatory cytokines, i.e., TNF-α and IFN-γ, in combination are known to induce cell death in several cell types, including oligodendrocytes, but the mechanism of their synergistic cytotoxicity is unclear. Although ceramide (Cer) has been implicated in cytokine- and stress-induced cell death, its intracellular levels alone cannot explain cytokine synergy. We considered the possibility that Cer released as part of extracellular vesicles may contribute to cytokine-induced synergistic cell death. Using a human oligodendroglioma (HOG) cell line as a model, here we show that exosomes derived from TNF-α-treated "donor" cells, while being mildly toxic to fresh cultures (similar to individual cytokines), induce enhanced cell death when added to IFN-γ-primed target cultures in a fashion resembling the effect of cytokine combination. Further, the sphingolipid profiles of secreted exosomes, as determined by HPLC-MS/MS, revealed that the treatment with the cytokines time-dependently induced the formation and exosomal release, in particular of C16-, C24-, and C24:1-Cer species; C16-, C24-, and C24:1-dihydroCer species; and C16-, C24-, and C24:1-SM species. Finally, exogenous C6-Cer or C16-Cer mimicked and enhanced the cytotoxic effects of the cytokines upon HOG cells, thereby supporting the cell death-signaling role of extracellular Cer.

Indexed as

Cell DeathCell Line, TumorCeramidesChromatography, High Pressure LiquidExosomesExtracellular VesiclesHumansInterferon-gammaOligodendrogliaOligodendrogliomaSphingolipidsTandem Mass SpectrometryTumor Necrosis Factor-alphaCeramidesInterferon-gammaSphingolipidsTumor Necrosis Factor-alphacell signalinglipidomicsmultiple sclerosisoligodendrocytesphingolipidsvesicles

Identifiers

PMID27623848
PMCPMC5087870
OpenAlexW2518704280

What OpenQuestion holds

Textmetadata
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.