Evidence map›Paper›PMID 38994992›Full record

ArticleCells2024

Mild Hyperthermia-Induced Thermogenesis in the Endoplasmic Reticulum Defines Stress Response Mechanisms.

Barbara Dukic, Zsófia Ruppert, Melinda E Tóth, Ákos Hunya, Ágnes Czibula, Péter Bíró, Ádám Tiszlavicz, Mária Péter, Gábor Balogh, Miklós Erdélyi and 4 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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

14 authors.

Barbara DukicLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.
Zsófia RuppertLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.ORCID 0009-0003-8543-7198
Melinda E TóthLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.
Ákos HunyaLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.ORCID 0000-0002-4547-9284
Ágnes CzibulaLaboratory of DNA Damage and Nuclear Dynamics, Institute of Genetics, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.ORCID 0000-0003-4461-2773
Péter BíróDepartment of Optics and Quantum Electronics, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0001-8103-6248
Ádám TiszlaviczLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.
Mária PéterLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.
Gábor BaloghLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.ORCID 0000-0002-4565-6850
Miklós ErdélyiDepartment of Optics and Quantum Electronics, University of Szeged, 6720 Szeged, Hungary.
Gyula TiminszkyLaboratory of DNA Damage and Nuclear Dynamics, Institute of Genetics, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.
László VíghLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.ORCID 0000-0001-7450-105X
Imre GombosLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.
Zsolt TörökLaboratory of Molecular Stress Biology, Institute of Biochemistry, HUN-REN Biological Research Centre, 6726 Szeged, Hungary.ORCID 0000-0003-0836-3247

Funding

Hungarian Research Network SA-72/2021Ministry of Culture and Innovation of Hungary from the National Research, Development and Innovation Fund TKP2021-NVA-19National Research Development and Innovation Office OTKA ANN 132280, OTKA K 135759, OTKA K 143248
6 · The paper itself

Abstract

Previous studies reported that a mild, non-protein-denaturing, fever-like temperature increase induced the unfolded protein response (UPR) in mammalian cells. Our dSTORM super-resolution microscopy experiments revealed that the master regulator of the UPR, the IRE1 (inositol-requiring enzyme 1) protein, is clustered as a result of UPR activation in a human osteosarcoma cell line (U2OS) upon mild heat stress. Using ER thermo yellow, a temperature-sensitive fluorescent probe targeted to the endoplasmic reticulum (ER), we detected significant intracellular thermogenesis in mouse embryonic fibroblast (MEF) cells. Temperatures reached at least 8 °C higher than the external environment (40 °C), resulting in exceptionally high ER temperatures similar to those previously described for mitochondria. Mild heat-induced thermogenesis in the ER of MEF cells was likely due to the uncoupling of the Ca

Indexed as

Endoplasmic ReticulumHeat-Shock ResponseThermogenesisAnimalsCell Line, TumorEndoplasmic Reticulum StressFibroblastsHumansHyperthermiaMiceProtein Serine-Threonine KinasesSarcoplasmic Reticulum Calcium-Transporting ATPasesUnfolded Protein ResponseProtein Serine-Threonine KinasesSarcoplasmic Reticulum Calcium-Transporting ATPasesflow cytometryfluorescence microscopyheat-shock responsehuman osteosarcoma cellsmild heatmouse embryonic fibroblast cellsorganelle temperatureRT-qPCRspectrofluorometrysuper-resolution microscopythermogenesisunfolded protein response

Identifiers

PMID38994992
PMCPMC11240596

What OpenQuestion holds

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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.