Evidence map›Paper›PMID 40333654›Full record

ArticlePloS one2025

Inositol-Requiring Enzyme 1 pathway and autophagy drive sequential response of endothelial cells to febrile range hyperthermia.

Julie Vorbe, Florence Massey, Corinne Rocher, Océane Morales, Nihal Brikci, Marie Le Borgne, Caligiuri Giuseppina, Antonino Nicoletti, Grégory Franck, Stéphane Illiano

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Julie VorbeUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.
Florence MasseyTranslational Sciences Department Sanofi- R&D, 1, avenue Pierre Brossolette, Chilly-Mazarin, France.
Corinne RocherTranslational Sciences Department Sanofi- R&D, 1, avenue Pierre Brossolette, Chilly-Mazarin, France.
Océane MoralesUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.
Nihal BrikciUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.
Marie Le BorgneUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.ORCID 0000-0002-3439-4867
Caligiuri GiuseppinaUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.
Antonino NicolettiUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.
Grégory FranckUniversité Paris Cité and Université Sorbonne Paris Nord, INSERM, LVTS, F-75018, Paris, France.ORCID 0000-0002-4288-9034
Stéphane IllianoCardiovascular Department Sanofi R&D, 1, avenue Pierre Brossolette, Chilly-Mazarin, France.ORCID 0000-0001-9196-0493

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextFever is an evolutionarily conserved and adaptive response during infections. However, prolonged fever has numerous systemic metabolic and functional side effects. In the heart, prolonged fever associated with infection is linked to fatal adverse effects, particularly involving impaired coronary circulation. Yet, the direct relationship between elevated temperature and coronary microcirculation dysfunction, remains to be fully demonstrated. In this study, we aimed to explore the specific responses of human coronary artery endothelial cells (HCAECs) to fever-range hyperthermia.

methodHCAECs were cultured at either 37°C or 40°C for up to 24 hours. Transcriptomic and proteomic profiles were obtained through microarray and mass spectrometry after 6, 12, and 24 hours of exposure. Key signaling pathways, upstream regulators, and candidate mechanisms were identified and validated at the mRNA and protein levels using mechanistic approaches.

resultsProlonged hyperthermia compromised HCAEC function, evidenced by cell detachment, loss of junctions, and increased permeability. HCAECs rapidly activated the unfolded protein response (UPR), including IRE1α activation and XBP1 splicing. Additionally, autophagic flux was significantly elevated, participating in the degradation of junction proteins. Pharmacological inhibition of IRE1α reduced the autophagic burden, protected against cell detachment, and preserved junction integrity over time.

conclusionOur findings reveal that in response to fever-range hyperthermia, the IRE1α-autophagy axis regulates the survival and function of coronary endothelial cells. This mechanism could play a key role in modulating endothelial responses during infection and contribute to the pathological outcomes of fever. Furthermore, it may be relevant in local inflammatory conditions with elevated temperatures.

Indexed as

AutophagyEndoribonucleasesEndothelial CellsFeverHyperthermiaProtein Serine-Threonine KinasesCells, CulturedCoronary VesselsHumansSignal TransductionUnfolded Protein ResponseX-Box Binding Protein 1EndoribonucleasesERN1 protein, humanProtein Serine-Threonine KinasesX-Box Binding Protein 1

Identifiers

PMID40333654
PMCPMC12057933

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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.