Evidence map›Paper›PMID 32811811›Full record

ArticleCell death & disease2020

MICAL2 is essential for myogenic lineage commitment.

Nefele Giarratana, Filippo Conti, Rita La Rovere, Rik Gijsbers, Paolo Carai, Robin Duelen, Tim Vervliet, Geert Bultynck, Flavio Ronzoni, Roberto Piciotti and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Structural basis of MICAL autoinhibition.Nature communications · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Myoblast 3D bioprinting to burst in vitro skeletal muscle differentiation.Journal of tissue engineering and regenerative medicine · 2022
    Article
  11. Review
  12. Article
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  14. Article
  15. Article
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  19. 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

16 authors at 6 institutions in 2 countries.

Nefele GiarratanaTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Filippo ContiTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Rita La RovereLaboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, and Leuven Kanker Instituut, KU, Leuven, 3000, Belgium.
Rik GijsbersLaboratory for Molecular Virology and Gene therapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Paolo CaraiDepartment of Cardiovascular Sciences, KU Leuven, 3000, Leuven, Belgium.
Robin DuelenTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0003-0904-1215
Tim VervlietLaboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, and Leuven Kanker Instituut, KU, Leuven, 3000, Belgium.
Geert BultynckLaboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine, and Leuven Kanker Instituut, KU, Leuven, 3000, Belgium.ORCID http://orcid.org/0000-0002-5968-4828
Flavio RonzoniHuman Anatomy Unit, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Roberto PiciottiTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Domiziana CostamagnaTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Stefania FulleDepartment of Neuroscience, Imaging and Clinical Sciences, Interuniversity Institute of Miology (IIM), University "G d'Annunzio", Chieti, Italy.ORCID http://orcid.org/0000-0003-4557-9127
Ivana BarravecchiaMedLab, Institute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Debora AngeloniMedLab, Institute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Yvan TorrenteStem Cell Laboratory, Department of Pathophysiology and Transplantation, University of Milan, Unit of Neurology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Centro Dino Ferrari, Milan, Italy.
Maurilio SampaolesiTranslational Cardiomyology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium. maurilio.sampaolesi@kuleuven.be.ORCID http://orcid.org/0000-0002-2422-3757
KU Leuven · BEUniversity of Pavia · ITScuola Superiore Sant'Anna · ITUniversity of Milan · ITHumanitas University · ITUniversity of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contractile myofiber units are mainly composed of thick myosin and thin actin (F-actin) filaments. F-Actin interacts with Microtubule Associated Monooxygenase, Calponin And LIM Domain Containing 2 (MICAL2). Indeed, MICAL2 modifies actin subunits and promotes actin filament turnover by severing them and preventing repolymerization. In this study, we found that MICAL2 increases during myogenic differentiation of adult and pluripotent stem cells (PSCs) towards skeletal, smooth and cardiac muscle cells and localizes in the nucleus of acute and chronic regenerating muscle fibers. In vivo delivery of Cas9-Mical2 guide RNA complexes results in muscle actin defects and demonstrates that MICAL2 is essential for skeletal muscle homeostasis and functionality. Conversely, MICAL2 upregulation shows a positive impact on skeletal and cardiac muscle commitments. Taken together these data demonstrate that modulations of MICAL2 have an impact on muscle filament dynamics and its fine-tuned balance is essential for the regeneration of muscle tissues.

Indexed as

Actin CytoskeletonActinsAnimalsCalponinsCell DifferentiationCytoskeletal ProteinsCytoskeletonFemaleMaleMiceMice, Inbred C57BLMuscle ContractionMuscle DevelopmentMuscle, SkeletalMuscle, SmoothMyosinsActinsCalponinsCytoskeletal ProteinsMical2 protein, mouseMyosins

Identifiers

PMID32811811
PMCPMC7434877
OpenAlexW3079678889

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.