Evidence map›Paper›PMID 38843936›Full record

ArticleLife science alliance2024

Mitochondrial lipidomes are tissue specific - low cholesterol contents relate to UCP1 activity.

Sarah Brunner, Marcus Höring, Gerhard Liebisch, Sabine Schweizer, Josef Scheiber, Piero Giansanti, Maria Hidrobo, Sven Hermeling, Josef Oeckl, Natalia Prudente de Mello and 9 more

Abstract read
In one paragraph

Article in Life science alliance, 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
–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

1 citing paper in PubMed.

  1. Review
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

19 authors.

Sarah BrunnerInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Marcus HöringInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Gerhard LiebischInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Sabine SchweizerZIEL Institute for Food & Health, Research Group Lipid Metabolism, Technical University of Munich, Freising, Germany.ORCID 0009-0000-7406-5294
Josef ScheiberBioVariance GmbH, Waldsassen, Germany.
Piero GiansantiBavarian Center for Biomolecular Mass Spectrometry at the University Hospital rechts der Isar, Technical University of Munich, Munich, Germany.ORCID 0000-0003-2857-0841
Maria HidroboZIEL Institute for Food & Health, Research Group Lipid Metabolism, Technical University of Munich, Freising, Germany.ORCID 0000-0002-6608-0088
Sven HermelingInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.ORCID 0009-0004-8323-3228
Josef OecklChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.
Natalia Prudente de MelloInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC), Helmholtz Zentrum München and German National Diabetes Center (DZD), Neuherberg, Germany.
Fabiana PerocchiInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC), Helmholtz Zentrum München and German National Diabetes Center (DZD), Neuherberg, Germany.ORCID 0000-0002-1102-6500
Claudine SeeligerZIEL Institute for Food & Health, Research Group Lipid Metabolism, Technical University of Munich, Freising, Germany.
Akim StrohmeyerChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.ORCID 0000-0003-3650-9661
Martin KlingensporChair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.ORCID 0000-0002-4502-6664
Johannes PlaggeZIEL Institute for Food & Health, Research Group Lipid Metabolism, Technical University of Munich, Freising, Germany.
Bernhard KüsterChair of Proteomics and Bioanalytics, Technical University of Munich, Freising, Germany.
Ralph BurkhardtInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.ORCID 0000-0003-1924-1202
Klaus-Peter JanssenDepartment of Surgery, School of Medicine, University Hospital rechts der Isar, Technical University of Munich, Munich Germany.
Josef EckerInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany josef.ecker@ukr.de.ORCID 0000-0003-4799-0788

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid composition is conserved within sub-cellular compartments to maintain cell function. Lipidomic analyses of liver, muscle, white and brown adipose tissue (BAT) mitochondria revealed substantial differences in their glycerophospholipid (GPL) and free cholesterol (FC) contents. The GPL to FC ratio was 50-fold higher in brown than white adipose tissue mitochondria. Their purity was verified by comparison of proteomes with ER and mitochondria-associated membranes. A lipid signature containing PC and FC, calculated from the lipidomic profiles, allowed differentiation of mitochondria from BAT of mice housed at different temperatures. Elevating FC in BAT mitochondria prevented uncoupling protein (UCP) 1 function, whereas increasing GPL boosted it. Similarly,

Indexed as

Adipose Tissue, BrownCholesterolLipidomicsMitochondriaUncoupling Protein 1Adipose Tissue, WhiteAnimalsGlycerophospholipidsLipid MetabolismMaleMiceMice, Inbred C57BLOrgan SpecificityCholesterolGlycerophospholipidsUcp1 protein, mouseUncoupling Protein 1

Identifiers

PMID38843936
PMCPMC11157264

What OpenQuestion holds

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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.