Evidence map›Paper›PMID 26248268›Full record

ReviewNature medicine2015

The central role of muscle stem cells in regenerative failure with aging.

Helen M Blau, Benjamin D Cosgrove, Andrew T V Ho

Open access · greenAbstract readReview
In one paragraph

Review in Nature medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 272 papers.

0numbers the graph read from it
0cells of the map it votes in
272citing papers in PubMed
18.1field-weighted citation impact, top 1% 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

272 citing papers in PubMed, 434 citations in OpenAlex.

  1. Trial
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  8. Article
  9. Alterations of actin in aging.Journal of cell science · 2026
    Review
  10. Article
  11. Review
  12. 15-PGDH inhibition promotes muscle repair and strength recovery during GLP-1 receptor agonist-induced weight loss.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  13. Article
  14. Review
  15. Article
  16. Article
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  18. Review
  19. Antisense Oligonucleotide Therapeutics Targeting Age-Related Diseases.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  20. Article

212 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Helen M BlauBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA.
Benjamin D CosgroveMeinig School of Biomedical Engineering, Cornell University, Ithaca, New York, USA.
Andrew T V HoBaxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA.
Stanford University · USCornell University · US

Funding

Basic and Translational Research iPSC-based hematologic and vascular therapiesU01HL100397 · NHLBI · STANFORD UNIVERSITY · PI COOKE, JOHN P · 2009 to 2015
$7.4M
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
Telomere extension using nucleoside-modified mRNA and exosomes as a novel therapeR01AR063963 · NIAMS · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2012 to 2016
$4.3M
Mass Cytometry Analysis of Signaling Dysfunction in Duchenne Muscular DystrophyR01NS089533 · NINDS · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2014 to 2017
$1.3M
Supplement to: EX VIVO REJUVENATION AND EXPANSION OF MUSCLE STEM CELLS FROM AGED MICER00AG042491 · NIA · CORNELL UNIVERSITY · PI COSGROVE, BENJAMIN DAVID · 2014 to 2016
$790k
Safe, Rapid Telomere Extension to Prevent and Treat HypertensionR21AG044815 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2013 to 2014
$434k
NHLBI NIH HHS U01 HL100397NIAMS NIH HHS AR063963NIAMS NIH HHS R01 AR063963NIA NIH HHS AG020961NIA NIH HHS AG044815NIA NIH HHS R00 AG042491NIA NIH HHS R00AG042491NIA NIH HHS R01 AG009521NIA NIH HHS R01 AG020961NIA NIH HHS R21 AG044815NINDS NIH HHS NS089533NINDS NIH HHS R01 NS089533
6 · The paper itself

Abstract

Skeletal muscle mass, function, and repair capacity all progressively decline with aging, restricting mobility, voluntary function, and quality of life. Skeletal muscle repair is facilitated by a population of dedicated muscle stem cells (MuSCs), also known as satellite cells, that reside in anatomically defined niches within muscle tissues. In adult tissues, MuSCs are retained in a quiescent state until they are primed to regenerate damaged muscle through cycles of self-renewal divisions. With aging, muscle tissue homeostasis is progressively disrupted and the ability of MuSCs to repair injured muscle markedly declines. Until recently, this decline has been largely attributed to extrinsic age-related alterations in the microenvironment to which MuSCs are exposed. However, as highlighted in this Perspective, recent reports show that MuSCs also progressively undergo cell-intrinsic alterations that profoundly affect stem cell regenerative function with aging. A more comprehensive understanding of the interplay of stem cell-intrinsic and extrinsic factors will set the stage for improving cell therapies capable of restoring tissue homeostasis and enhancing muscle repair in the aged.

Indexed as

AgingAnimalsBone Morphogenetic ProteinsCell PolarityCellular SenescenceGrowth Differentiation FactorsHomeostasisHumansInflammationMuscle, Skeletalp38 Mitogen-Activated Protein KinasesRegenerationStem CellsBone Morphogenetic ProteinsGDF11 protein, humanGrowth Differentiation Factorsp38 Mitogen-Activated Protein Kinases

Identifiers

PMID26248268
PMCPMC4731230
OpenAlexW2230902569

What OpenQuestion holds

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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.