Evidence map›Paper›PMID 26243583›Full record

ArticleNature communications2015

Turning terminally differentiated skeletal muscle cells into regenerative progenitors.

Heng Wang, Sara Lööf, Paula Borg, Gustavo A Nader, Helen M Blau, András Simon

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. The salamander blastema within the broader context of metazoan regeneration.Frontiers in cell and developmental biology · 2023
    Review
  14. MAPK/ERK Pathway as a Central Regulator in Vertebrate Organ Regeneration.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Cell Cycle Proteins as Key Regulators of Postmitotic Cell Death.The Yale journal of biology and medicine · 2019
    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

6 authors at 2 institutions in 2 countries.

Heng WangDepartment of Cell and Molecular Biology, Karolinska Institute, Solna, Sweden.
Sara LööfDepartment of Cell and Molecular Biology, Karolinska Institute, Solna, Sweden.
Paula BorgDepartment of Cell and Molecular Biology, Karolinska Institute, Solna, Sweden.
Gustavo A NaderDepartment of Physiology and Pharmacology, Karolinska Institute, 17177 Stockholm, Sweden.
Helen M BlauBaxter Laboratory for Stem Cell Biology, Stanford University, Stanford, California 94305, United States.
András SimonDepartment of Cell and Molecular Biology, Karolinska Institute, Solna, Sweden.
Karolinska Institutet · SEStanford University · US

Funding

Stem Cells for Brain and BrawnR01AG020961 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2002 to 2019
$5.0M
ACTIVATORS OF MUSCLE GENESR01AG009521 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 1990 to 2014
$4.7M
REGULATION OF MUSCLE DEVELOPMENTR01HD018179 · NICHD · STANFORD UNIVERSITY · PI BLAU, HELEN M · 1985 to 2007
$2.7M
Regulator of Adult Stem Cell FateR01AG024987 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2004 to 2008
$1.7M
NIA NIH HHS R01 AG009521NIA NIH HHS R01 AG020961NIA NIH HHS R01 AG024987NICHD NIH HHS R01 HD018179
6 · The paper itself

Abstract

The ability to repeatedly regenerate limbs during the entire lifespan of an animal is restricted to certain salamander species among vertebrates. This ability involves dedifferentiation of post-mitotic cells into progenitors that in turn form new structures. A long-term enigma has been how injury leads to dedifferentiation. Here we show that skeletal muscle dedifferentiation during newt limb regeneration depends on a programmed cell death response by myofibres. We find that programmed cell death-induced muscle fragmentation produces a population of 'undead' intermediate cells, which have the capacity to resume proliferation and contribute to muscle regeneration. We demonstrate the derivation of proliferating progeny from differentiated, multinucleated muscle cells by first inducing and subsequently intercepting a programmed cell death response. We conclude that cell survival may be manifested by the production of a dedifferentiated cell with broader potential and that the diversion of a programmed cell death response is an instrument to achieve dedifferentiation.

Indexed as

Cell DedifferentiationRegenerationAnimalsCaspasesCell DeathCell ProliferationFemaleMice, Inbred NODMice, SCIDMuscle Fibers, SkeletalMuscle, SkeletalNotophthalmus viridescensCaspases

Identifiers

PMID26243583
PMCPMC4765497
OpenAlexW2259462781

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.