Evidence map›Paper›PMID 32212902›Full record

ArticleCirculation research2020

A Critical Role for Estrogen-Related Receptor Signaling in Cardiac Maturation.

Tomoya Sakamoto, Timothy R Matsuura, Shibiao Wan, David M Ryba, J Unil Kim, Kyoung Jae Won, Ling Lai, Christopher Petucci, Nataliya Petrenko, Kiran Musunuru and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 3 pooled it
13.3field-weighted citation impact, top 1% 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

95 citing papers in PubMed, 3 syntheses or guidelines pooled it, 143 citations in OpenAlex.

  1. Pooled it
  2. Engineering the maturation of stem cell-derived cardiomyocytes.Frontiers in bioengineering and biotechnology · 2023
    Pooled it
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35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Tomoya Sakamoto *From the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Timothy R Matsuura *From the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Shibiao WanInstitute for Diabetes, Obesity and Metabolism, Department of Medicine (S.W., J.K., K.J.W.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
David M RybaFrom the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
J Unil KimInstitute for Diabetes, Obesity and Metabolism, Department of Medicine (S.W., J.K., K.J.W.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Kyoung Jae WonInstitute for Diabetes, Obesity and Metabolism, Department of Medicine (S.W., J.K., K.J.W.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Ling LaiFrom the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Christopher PetucciFrom the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Nataliya PetrenkoFrom the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Kiran MusunuruFrom the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Rick B VegaCenter for Metabolic Origins of Disease, Sanford Burnham Prebys Medical Discovery Institute at Lake Nona, Orlando, FL (R.B.V.).
Daniel P KellyFrom the Cardiovascular Institute (T.S., T.R.M., D.M.R., L.L., C.P., N.P., K.M., D.P.K.).
Cardiovascular Institute of the South · USUniversity of Copenhagen · DKSanford Burnham Prebys Medical Discovery Institute · USSt. Jude Children's Research Hospital · US

Funding

VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Patrick Seale · 1986 to 2026
$48.3M
Training Program in Cardiovascular Biology and MedicineT32HL007843 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI THOMAS P. CAPPOLA, Sharlene M Day · 1996 to 2026
$11.0M
REGULATION OF FATTY ACID OXIDATION DURING CARDIAC GROWTHR01HL058493 · NHLBI · WASHINGTON UNIVERSITY · PI KELLY, DANIEL PATRICK · 1998 to 2024
$10.6M
Multidisciplinary Training in Cardiovascular BiologyT32HL007954 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI DAVIES, PETER FRANCIS · 2000 to 2019
$9.9M
NHLBI NIH HHS R01 HL058493NHLBI NIH HHS T32 HL007843NHLBI NIH HHS T32 HL007954NIDDK NIH HHS P30 DK019525
6 · The paper itself

Abstract

rationaleThe heart undergoes dramatic developmental changes during the prenatal to postnatal transition, including maturation of cardiac myocyte energy metabolic and contractile machinery. Delineation of the mechanisms involved in cardiac postnatal development could provide new insight into the fetal shifts that occur in the diseased heart and unveil strategies for driving maturation of stem cell-derived cardiac myocytes.

objectiveTo delineate transcriptional drivers of cardiac maturation. METHODS AND

resultsWe hypothesized that ERR (estrogen-related receptor) α and γ, known transcriptional regulators of postnatal mitochondrial biogenesis and function, serve a role in the broader cardiac maturation program. We devised a strategy to knockdown the expression of ERRα and γ in heart after birth (pn-csERRα/γ [postnatal cardiac-specific ERRα/γ]) in mice. With high levels of knockdown, pn-csERRα/γ knockdown mice exhibited cardiomyopathy with an arrest in mitochondrial maturation. RNA sequence analysis of pn-csERRα/γ knockdown hearts at 5 weeks of age combined with chromatin immunoprecipitation with deep sequencing and functional characterization conducted in human induced pluripotent stem cell-derived cardiac myocytes (hiPSC-CM) demonstrated that ERRγ activates transcription of genes involved in virtually all aspects of postnatal developmental maturation, including mitochondrial energy transduction, contractile function, and ion transport. In addition, ERRγ was found to suppress genes involved in fibroblast activation in hearts of pn-csERRα/γ knockdown mice. Disruption of

conclusionsERRα and γ are critical regulators of cardiac myocyte maturation, serving as transcriptional activators of adult cardiac metabolic and structural genes, an.d suppressors of noncardiac lineages including fibroblast determination.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCells, CulturedERRalpha Estrogen-Related ReceptorGene Expression Regulation, DevelopmentalHeartHumansInduced Pluripotent Stem CellsMiceMitochondria, HeartMyocytes, CardiacReceptors, EstrogenSignal TransductionBasic Helix-Loop-Helix ProteinsERRalpha Estrogen-Related ReceptorEsrrg protein, mouseReceptors, EstrogenTcf21 protein, mousecardiomyocytescell differentiationfibroblastsgenetic transcriptionmitochondriapostnatal cardiac development

Identifiers

PMID32212902
PMCPMC7274895
OpenAlexW3012989083

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.