Evidence map›Paper›PMID 29670077›Full record

ArticleNature communications2018

Induction of muscle stem cell quiescence by the secreted niche factor Oncostatin M.

Srinath C Sampath, Srihari C Sampath, Andrew T V Ho, Stéphane Y Corbel, Joshua D Millstone, John Lamb, John Walker, Bernd Kinzel, Christian Schmedt, Helen M Blau

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.1field-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

58 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. RhoA-mediated GCell discovery · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 4 institutions in 3 countries.

Srinath C SampathBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA. ssampath@gnf.org.
Srihari C SampathBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Andrew T V HoBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Stéphane Y CorbelBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Joshua D MillstoneGenomics Institute of the Novartis Research Foundation, San Diego, CA, 92121, USA.ORCID http://orcid.org/0000-0002-1488-8763
John LambGenomics Institute of the Novartis Research Foundation, San Diego, CA, 92121, USA.
John WalkerGenomics Institute of the Novartis Research Foundation, San Diego, CA, 92121, USA.
Bernd KinzelNovartis Institutes for BioMedical Research, 4056, Basel, Switzerland.
Christian SchmedtGenomics Institute of the Novartis Research Foundation, San Diego, CA, 92121, USA.
Helen M BlauBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA. hblau@stanford.edu.
Genomics Institute of the Novartis Research Foundation · USInstitute for Stem Cell Biology and Regenerative Medicine · INNovartis (Switzerland) · CHStanford University · US

Funding

Stem Cells for Brain and BrawnR01AG020961 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2002 to 2019
$5.0M
Mass Cytometry Analysis of Signaling Dysfunction in Duchenne Muscular DystrophyR01NS089533 · NINDS · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2014 to 2017
$1.3M
NIA NIH HHS R01 AG020961NIH HHS R01 AG020961NIH HHS R01 NS089533
6 · The paper itself

Abstract

The balance between stem cell quiescence and proliferation in skeletal muscle is tightly controlled, but perturbed in a variety of disease states. Despite progress in identifying activators of stem cell proliferation, the niche factor(s) responsible for quiescence induction remain unclear. Here we report an in vivo imaging-based screen which identifies Oncostatin M (OSM), a member of the interleukin-6 family of cytokines, as a potent inducer of muscle stem cell (MuSC, satellite cell) quiescence. OSM is produced by muscle fibers, induces reversible MuSC cell cycle exit, and maintains stem cell regenerative capacity as judged by serial transplantation. Conditional OSM receptor deletion in satellite cells leads to stem cell depletion and impaired regeneration following injury. These results identify Oncostatin M as a secreted niche factor responsible for quiescence induction, and for the first time establish a direct connection between induction of quiescence, stemness, and transplantation potential in solid organ stem cells.

Indexed as

AllelesAnimalsCell CycleCell DifferentiationCell DivisionCell LineCell ProliferationFemaleHumansInterleukin-6LuminescenceMiceMice, Inbred C57BLMuscle Fibers, SkeletalMuscle, SkeletalOligonucleotide Array Sequence AnalysisInterleukin-6interleukin-6, mouseOncostatin M

Identifiers

PMID29670077
PMCPMC5906564
OpenAlexW2952817372

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.