Evidence map›Paper›PMID 30745033›Full record

ArticleStem cell reports2019

Combined Notch and PDGF Signaling Enhances Migration and Expression of Stem Cell Markers while Inducing Perivascular Cell Features in Muscle Satellite Cells.

Mattia Francesco Maria Gerli, Louise Anne Moyle, Sara Benedetti, Giulia Ferrari, Ekin Ucuncu, Martina Ragazzi, Chrystalla Constantinou, Irene Louca, Hiroshi Sakai, Pierpaolo Ala and 4 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Lineage tracing reveals a novel PDGFRβScientific reports · 2024
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  8. Schwann Cells Are Key Regulators of Corneal Epithelial Renewal.Investigative ophthalmology & visual science · 2023
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  9. Article
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  14. Article
  15. Review
  16. Regulatory role of RNA NFrontiers in cell and developmental biology · 2022
    Review
  17. Review
  18. METTL3-Mediated mStem cells international · 2021
    Article
  19. Review
  20. 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

14 authors at 6 institutions in 2 countries.

Mattia Francesco Maria GerliDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK; Stem Cell and Regenerative Medicine Section, Great Ormond Street Institute of Child Health, University College London, WC1N 1EH London, UK.
Louise Anne MoyleDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK.
Sara BenedettiDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK; Molecular and Cellular Immunology Section, Great Ormond Street Institute of Child Health, University College London, WC1N 1EH London, UK; NIHR Great Ormond Street Hospital Biomedical Research Centre, WC1N 1EH London, UK.
Giulia FerrariDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK.
Ekin UcuncuDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK.
Martina RagazziDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK.
Chrystalla ConstantinouDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK.
Irene LoucaDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK.
Hiroshi SakaiDepartment of Developmental & Stem Cell Biology, Institut Pasteur, 75015 Paris, France; CNRS UMR 3738, Institut Pasteur, 75015 Paris, France.
Pierpaolo AlaThe Dubowitz Neuromuscular Centre, Great Ormond Street Institute of Child Health, University College London, WC1N 1EH London, UK.
Paolo De CoppiStem Cell and Regenerative Medicine Section, Great Ormond Street Institute of Child Health, University College London, WC1N 1EH London, UK.
Shahragim TajbakhshDepartment of Developmental & Stem Cell Biology, Institut Pasteur, 75015 Paris, France; CNRS UMR 3738, Institut Pasteur, 75015 Paris, France.
Giulio CossuDivision of Cell Matrix Biology and Regenerative Medicine, University of Manchester, M13 9PL Manchester, UK.
Francesco Saverio TedescoDepartment of Cell and Developmental Biology, University College London, WC1E 6DE London, UK; The Dubowitz Neuromuscular Centre, Great Ormond Street Institute of Child Health, University College London, WC1N 1EH London, UK. Electronic address: f.s.tedesco@ucl.ac.uk.
University College London · GBGreat Ormond Street Hospital · GBCentre National de la Recherche Scientifique · FRInstitut Pasteur · FRNIHR Great Ormond Street Hospital Biomedical Research CentreUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J014567/1Biotechnology and Biological Sciences Research Council BB/M009513/1Biotechnology and Biological Sciences Research Council BB/N503915/1EPA EP-D-18-001Medical Research Council MR/J006785/1Medical Research Council MR/L002752/1Medical Research Council MR/P016006/1Medical Research Council MR/R014108/1Medical Research Council MR/S015116/1
6 · The paper itself

Abstract

Satellite cells are responsible for skeletal muscle regeneration. Upon activation, they proliferate as transient amplifying myoblasts, most of which fuse into regenerating myofibers. Despite their remarkable differentiation potential, these cells have limited migration capacity, which curtails clinical use for widespread forms of muscular dystrophy. Conversely, skeletal muscle perivascular cells have less myogenic potential but better migration capacity than satellite cells. Here we show that modulation of Notch and PDGF pathways, involved in developmental specification of pericytes, induces perivascular cell features in adult mouse and human satellite cell-derived myoblasts. DLL4 and PDGF-BB-treated cells express markers of perivascular cells and associate with endothelial networks while also upregulating markers of satellite cell self-renewal. Moreover, treated cells acquire trans-endothelial migration ability while remaining capable of engrafting skeletal muscle upon intramuscular transplantation. These results extend our understanding of muscle stem cell fate plasticity and provide a druggable pathway with clinical relevance for muscle cell therapy.

Indexed as

AnimalsBiomarkersCell MovementEndothelial CellsHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, Inbred C57BLMuscle DevelopmentMuscle, SkeletalMyoblastsPericytesReceptors, NotchReceptors, Platelet-Derived Growth FactorRegenerationBiomarkersdelta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchReceptors, Platelet-Derived Growth Factorcell therapymuscle regenerationmuscle stem cellsmuscular dystrophyNOTCHPDGFperivascular cellsreprogrammingsatellite cellsstem cell fate

Identifiers

PMID30745033
PMCPMC6409426
OpenAlexW2913486325

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.