Evidence map›Paper›PMID 29093487›Full record

ArticleNature communications2017

MicroRNAs promote skeletal muscle differentiation of mesodermal iPSC-derived progenitors.

Giorgia Giacomazzi, Bryan Holvoet, Sander Trenson, Ellen Caluwé, Bojana Kravic, Hanne Grosemans, Álvaro Cortés-Calabuig, Christophe M Deroose, Danny Huylebroeck, Said Hashemolhosseini and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  5. Excess PrPNature communications · 2023
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  16. Molecular therapy. Methods & clinical development · 2020
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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 at 6 institutions in 5 countries.

Giorgia GiacomazziTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, 3000, Leuven, Belgium.
Bryan HolvoetDepartment of Imaging and Pathology, Nuclear Medicine and Molecular Imaging, KU Leuven, 3000, Leuven, Belgium.
Sander TrensonDepartment of Cardiovascular Sciences, KU Leuven, 3000, Leuven, Belgium.
Ellen CaluwéDepartment of Cardiovascular Sciences, KU Leuven, 3000, Leuven, Belgium.
Bojana KravicInstitute of Biochemistry, Friedrich-Alexander University of Erlangen-Nürnberg, 91054, Erlangen, Germany.
Hanne GrosemansTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, 3000, Leuven, Belgium.
Álvaro Cortés-CalabuigGenomics core, Center for Human Genetics KU Leuven, 3000, Leuven, Belgium.
Christophe M DerooseDepartment of Imaging and Pathology, Nuclear Medicine and Molecular Imaging, KU Leuven, 3000, Leuven, Belgium.
Danny HuylebroeckDepartment of Cell Biology, Erasmus MC, 3015 CN, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-4862-1079
Said HashemolhosseiniInstitute of Biochemistry, Friedrich-Alexander University of Erlangen-Nürnberg, 91054, Erlangen, Germany.
Stefan JanssensDepartment of Cardiovascular Sciences, KU Leuven, 3000, Leuven, Belgium.
Elizabeth McNallyCenter for Genetic Medicine, Northwestern University, Chicago, IL, 60611, USA.
Mattia QuattrocelliTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, 3000, Leuven, Belgium.
Maurilio SampaolesiTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, 3000, Leuven, Belgium. maurilio.sampaolesi@med.kuleuven.be.ORCID http://orcid.org/0000-0002-2422-3757
KU Leuven · BEFriedrich-Alexander-Universität Erlangen-Nürnberg · DENorthwestern University · USErasmus MC · NLUniversity of Pavia · ITVIB-KU Leuven Center for Cancer Biology · BE

Funding

Training and education CoreU54AR052646 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI MCNALLY, ELIZABETH M, SWEENEY, H LEE · 2005 to 2020
$24.1M
SARCOGLYCAN IN MYOPATHY AND MUSCLE MEMBRANE STABILITYR01HL061322 · NHLBI · UNIVERSITY OF CHICAGO · PI MCNALLY, ELIZABETH M · 1999 to 2022
$7.5M
NHLBI NIH HHS R01 HL061322NIAMS NIH HHS U54 AR052646
6 · The paper itself

Abstract

Muscular dystrophies (MDs) are often characterized by impairment of both skeletal and cardiac muscle. Regenerative strategies for both compartments therefore constitute a therapeutic avenue. Mesodermal iPSC-derived progenitors (MiPs) can regenerate both striated muscle types simultaneously in mice. Importantly, MiP myogenic propensity is influenced by somatic lineage retention. However, it is still unknown whether human MiPs have in vivo potential. Furthermore, methods to enhance the intrinsic myogenic properties of MiPs are likely needed, given the scope and need to correct large amounts of muscle in the MDs. Here, we document that human MiPs can successfully engraft into the skeletal muscle and hearts of dystrophic mice. Utilizing non-invasive live imaging and selectively induced apoptosis, we report evidence of striated muscle regeneration in vivo in mice by human MiPs. Finally, combining RNA-seq and miRNA-seq data, we define miRNA cocktails that promote the myogenic potential of human MiPs.

Indexed as

AnimalsCell DifferentiationEchocardiographyHeartHumansInduced Pluripotent Stem CellsMesodermMiceMicroRNAsMuscle DevelopmentMuscle, SkeletalMuscular Dystrophy, AnimalMyocardiumRegenerationMicroRNAs

Identifiers

PMID29093487
PMCPMC5665910
OpenAlexW2766290258

What OpenQuestion holds

Textmetadata
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.