Evidence map›Paper›PMID 38019121›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2024

Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF.

Eike C Struck, Tatiana Belova, Ping-Han Hsieh, Jacob O Odeberg, Marieke L Kuijjer, Philip J Dusart, Lynn M Butler

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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 5 institutions in 3 countries.

Eike C StruckDepartment of Clinical Medicine, The Arctic University of Norway, Tromsø, Norway.
Tatiana BelovaCentre for Molecular Medicine Norway, Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Ping-Han HsiehCentre for Molecular Medicine Norway, Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Jacob O OdebergDepartment of Clinical Medicine, The Arctic University of Norway, Tromsø, Norway.
Marieke L KuijjerCentre for Molecular Medicine Norway, Nordic EMBL Partnership, University of Oslo, Oslo, Norway.ORCID 0000-0001-6280-3130
Philip J DusartScience for Life Laboratory, Department of Protein Science, Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0003-2747-3214
Lynn M ButlerDepartment of Clinical Medicine, The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0002-2352-8217
University of Oslo · NOArctic Research Centre · SEKarolinska University Hospital · SEScience for Life Laboratory · SEUniversity Hospital of North Norway · NO

Funding

Hjärt-Lungfonden (Swedish Heart-Lung Foundation) 20170759Stockholm läns landsting (Stockholm County Council) SLL 2017-0842Vetenskapsrådet (VR) 2019-01493
6 · The paper itself

Abstract

The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-course analysis of the human EC response to TNF, from 30 min to 72 h. We identified regulated genes and used weighted gene network correlation analysis to decipher coexpression profiles, uncovering two distinct temporal phases: an acute response (between 1 and 4 h) and a later phase (between 12 and 24 h). Sex-based subset analysis revealed that the response was comparable between female and male cells. Several previously uncharacterized genes were strongly regulated during the acute phase, whereas the majority in the later phase were IFN-stimulated genes. A lack of IFN transcription indicated that this IFN-stimulated gene expression was independent of de novo IFN production. We also observed two groups of genes whose transcription was inhibited by TNF: those that resolved toward baseline levels and those that did not. Our study provides insights into the global dynamics of the EC transcriptional response to TNF, highlighting distinct gene expression patterns during the acute and later phases. Data for all coding and noncoding genes is provided on the Web site (http://www.endothelial-response.org/). These findings may be useful in understanding the role of ECs in inflammation and in developing TNF signaling-targeted therapies.

Indexed as

Endothelium, VascularGene Expression ProfilingCells, CulturedEndothelial CellsFemaleHumansInflammationMaleSignal TransductionTumor Necrosis Factor-alphaTumor Necrosis Factor-alpha

Identifiers

PMID38019121
PMCPMC10733583
OpenAlexW4389136204

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.