Evidence map›Paper›PMID 32123818›Full record

ArticleFASEB bioAdvances2019

Regeneration competent satellite cell niches in rat engineered skeletal muscle.

Malte Tiburcy, Alex Markov, Lena K Kraemer, Peter Christalla, Margret Rave-Fraenk, Henrike J Fischer, Holger M Reichardt, Wolfram-Hubertus Zimmermann

Abstract read
In one paragraph

Article in FASEB bioAdvances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. A conciseFrontiers in cell and developmental biology · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Next Stage Approach to Tissue Engineering Skeletal Muscle.Bioengineering (Basel, Switzerland) · 2020
    Review
  17. Tissue-Engineered Human Myobundle System as a Platform for Evaluation of Skeletal Muscle Injury Biomarkers.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Article
  18. 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

8 authors.

Malte TiburcyInstitute of Pharmacology and Toxicology Georg-August University Göttingen Göttingen Germany.
Alex MarkovInstitute of Pharmacology and Toxicology Georg-August University Göttingen Göttingen Germany.
Lena K KraemerInstitute of Pharmacology and Toxicology Georg-August University Göttingen Göttingen Germany.
Peter ChristallaInstitute of Pharmacology and Toxicology Georg-August University Göttingen Göttingen Germany.
Margret Rave-FraenkDepartment of Radiation Therapy and Radiooncology Georg-August University Göttingen Göttingen Germany.
Henrike J FischerInstitute for Cellular and Molecular Immunology Georg-August University Göttingen Göttingen Germany.
Holger M ReichardtInstitute for Cellular and Molecular Immunology Georg-August University Göttingen Göttingen Germany.
Wolfram-Hubertus ZimmermannInstitute of Pharmacology and Toxicology Georg-August University Göttingen Göttingen Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Satellite cells reside in defined niches and are activated upon skeletal muscle injury to facilitate regeneration. Mechanistic studies of skeletal muscle regeneration are hampered by the inability to faithfully simulate satellite cell biology in vitro. We sought to overcome this limitation by developing tissue engineered skeletal muscle (ESM) with (1) satellite cell niches and (2) the capacity to regenerate after injury. ESMs contained quiescent Pax7-positive satellite cells in morphologically defined niches. Satellite cells could be activated to repair (i) cardiotoxin and (ii) mechanical crush injuries. Activation of the Wnt-pathway was essential for muscle regeneration. Finally, muscle progenitors from the engineered niche developed de novo ESM in vitro and regenerated skeletal muscle after cardiotoxin-induced injury in vivo. We conclude that ESM with functional progenitor niches reminiscent of the in vivo satellite cell niches can be engineered in vitro. ESM may ultimately be exploited in disease modeling, drug screening, or muscle regeneration.

Indexed as

Drug screeningMuscle repairNotch‐signalingSatellite cellSkeletal muscleTissue engineeringWnt‐signaling

Identifiers

PMID32123818
PMCPMC6996344

What OpenQuestion holds

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Registered trials

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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.