Evidence map›Paper›PMID 26923583›Full record

ArticleCell reports2016

Nfix Regulates Temporal Progression of Muscle Regeneration through Modulation of Myostatin Expression.

Giuliana Rossi, Stefania Antonini, Chiara Bonfanti, Stefania Monteverde, Chiara Vezzali, Shahragim Tajbakhsh, Giulio Cossu, Graziella Messina

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 82 citations in OpenAlex.

  1. Dynamic NFIX Promoter Usage Shapes Stem and Committed Myogenic States.International journal of molecular sciences · 2026
    Article
  2. Delpacibart etedesiran improves the molecular pathology of myotonic dystrophy type 1 in the phase 1/2 MARINA study.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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  10. Regulatory Role ofInternational journal of molecular sciences · 2024
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  14. Review
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  20. NFIXing Cancer: The Role of NFIX in Oxidative Stress Response and Cell Fate.International journal of molecular sciences · 2023
    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

8 authors at 3 institutions in 3 countries.

Giuliana RossiDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Stefania AntoniniDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Chiara BonfantiDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Stefania MonteverdeDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Chiara VezzaliDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Shahragim TajbakhshStem Cells and Development, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Institut Pasteur, 25 Rue du Dr. Roux, 75015 Paris, France.
Giulio CossuDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy; Institute of Inflammation and Repair, University of Manchester, Oxford Road, M13 9PL Manchester, UK.
Graziella MessinaDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy. Electronic address: graziella.messina@unimi.it.
University of Milan · ITInstitut Pasteur · FRUniversity of Manchester · GB

Funding

British Heart Foundation PG/14/1/30549
6 · The paper itself

Abstract

Nfix belongs to a family of four highly conserved proteins that act as transcriptional activators and/or repressors of cellular and viral genes. We previously showed a pivotal role for Nfix in regulating the transcriptional switch from embryonic to fetal myogenesis. Here, we show that Nfix directly represses the Myostatin promoter, thus controlling the proper timing of satellite cell differentiation and muscle regeneration. Nfix-null mice display delayed regeneration after injury, and this deficit is reversed upon in vivo Myostatin silencing. Conditional deletion of Nfix in satellite cells results in a similar delay in regeneration, confirming the functional requirement for Nfix in satellite cells. Moreover, mice lacking Nfix show reduced myofiber cross sectional area and a predominant slow twitching phenotype. These data define a role for Nfix in postnatal skeletal muscle and unveil a mechanism for Myostatin regulation, thus providing insights into the modulation of its complex signaling pathway.

Indexed as

RegenerationAnimalsCell DifferentiationCell LineCells, CulturedGene SilencingMice, TransgenicMuscle Fibers, SkeletalMyoblastsMyostatinNFI Transcription FactorsMstn protein, mouseMyostatinNFI Transcription FactorsNfix protein, mouseMyostatinNfixregenerationsatellite cellsskeletal muscle

Identifiers

PMID26923583
PMCPMC4793149
OpenAlexW2283793680

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.