Evidence map›Paper›PMID 39196021›Full record

ArticleNature cardiovascular research2023

Estrogen receptor alpha deficiency in cardiomyocytes reprograms the heart-derived extracellular vesicle proteome and induces obesity in female mice.

Yow Keat Tham, Bianca C Bernardo, Bethany Claridge, Gunes S Yildiz, Liesel Min-Linn Woon, Simon Bond, Haoyun Fang, Jenny Y Y Ooi, Aya Matsumoto, Jieting Luo and 18 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cardiovascular research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Review
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  15. Article
  16. Metabolic Messengers: oestradiol.Nature metabolism · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Comparative analysis of two independent Myh6-Cre transgenic mouse lines.Journal of molecular and cellular cardiology plus · 2024
    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

28 authors.

Yow Keat Tham *Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0002-9790-1926
Bianca C Bernardo *Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0002-4534-0549
Bethany ClaridgeBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0002-4589-1033
Gunes S YildizBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Liesel Min-Linn WoonBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Simon BondBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Haoyun FangBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Jenny Y Y OoiBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Aya MatsumotoBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0003-2137-1639
Jieting LuoBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Celeste M K TaiBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0002-5148-8929
Claudia A HarmawanBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Helen KiriazisBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Daniel G DonnerBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0003-4924-720X
Natalie A MellettBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
E Dale AbelDavid Geffen School of Medicine, University of California, Los Angeles, California, CA, USA.
Sohaib A KhanDepartment of Cancer Biology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
David P De SouzaMetabolomics Australia, Bio21 Institute, The University of Melbourne, Melbourne, Victoria, Australia.
Sheik Nadeem Elahee DoomunMetabolomics Australia, Bio21 Institute, The University of Melbourne, Melbourne, Victoria, Australia.ORCID 0000-0002-6384-859X
Kevin LiuBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Ruidong XiangBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Manika SinghBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Michael InouyeBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Peter J MeikleBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.ORCID 0000-0002-2593-4665
Kate L WeeksBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Brian G DrewBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
David W GreeningBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia. david.greening@baker.edu.au.ORCID 0000-0001-7516-485X
Julie R McMullenBaker Heart and Diabetes Institute, Melbourne, Victoria, Australia. julie.mcmullen@baker.edu.au.ORCID 0000-0002-8316-1066

Funding

American Heart Association (American Heart Association, Inc.) 20SFRN35120123Department of Health | National Health and Medical Research Council (NHMRC) 1057741Department of Health | National Health and Medical Research Council (NHMRC) 1078985Department of Health | National Health and Medical Research Council (NHMRC) 1139489National Heart Foundation of Australia (Heart Foundation) 102539National Heart Foundation of Australia (Heart Foundation) G 08M 3760
6 · The paper itself

Abstract

Dysregulation of estrogen receptor alpha (ERα) has been linked with increased metabolic and cardiovascular disease risk. Here, we generate and characterize cardiomyocyte-specific ERα knockout (ERαHKO) mice to assess the role of ERα in the heart. The most striking phenotype was obesity in female ERαHKO but not male ERαHKO mice. Female ERαHKO mice showed cardiac dysfunction, mild glucose and insulin intolerance and reduced ERα gene expression in skeletal muscle and white adipose tissue. Transcriptomic, proteomic, lipidomic and metabolomic analyses revealed evidence of contractile and/or metabolic dysregulation in heart, skeletal muscle and white adipose tissue. We show that heart-derived extracellular vesicles from female ERαHKO mice contain a distinct proteome associated with lipid and metabolic regulation, and have the capacity to metabolically reprogram the target skeletal myocyte proteome with functional impacts on glycolytic capacity and reserve. This multi-omics study uncovers a cardiac-initiated and sex-specific cardiometabolic phenotype regulated by ERα and provides insights into extracellular vesicle-mediated interorgan communication.

Indexed as

Estrogen Receptor alphaExtracellular VesiclesMice, KnockoutMyocytes, CardiacObesityProteomeAdipose Tissue, WhiteAnimalsDisease Models, AnimalEnergy MetabolismFemaleMaleMiceMice, Inbred C57BLMuscle, SkeletalPhenotypeEsr1 protein, mouseEstrogen Receptor alphaProteome

Identifiers

PMID39196021

What OpenQuestion holds

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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.