Evidence map›Paper›PMID 41350439›Full record

ArticleCommunications biology2025

Tenascin-C from the tissue microenvironment promotes muscle stem cell maintenance and function through Annexin A2.

Alessandra Cecchini, Mafalda Loreti, Collin D Kaufman, Cedomir Stamenkovic, Gabriele Guarnaccia, Alma Renero, Chiara Nicoletti, Anais Kervadec, Daphne Mayer, Shawn Delaware and 5 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Alessandra Cecchini *Cardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Mafalda Loreti *Cardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Collin D KaufmanCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0003-3676-3512
Cedomir StamenkovicCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Gabriele GuarnacciaCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Alma ReneroCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Chiara NicolettiCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-0872-6506
Anais KervadecCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Daphne MayerCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Shawn DelawareCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.ORCID http://orcid.org/0009-0000-3702-8638
Luca CaputoCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-1697-9968
Xiuqing WeiCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Alexandre ColasCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-8489-0570
Pier Lorenzo PuriCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0003-4964-0095
Alessandra SaccoCardiovascular and Muscular Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA. asacco@sbpdiscovery.org.ORCID http://orcid.org/0000-0003-1669-0221

Funding

Pathogenic Alterations of the 3D Epigenetic Landscape in Dystrophin-Deficient Skeletal Muscles and Reversal by Dystrophin Re-ExpressionR01AR056712 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Pier Lorenzo Puri · 2009 to 2026
$7.3M
Role of Fbxw7-Mediated Proteasomal Degradation in Myofibers in Determining Muscle Stem Cell Pool SizeR01AR077448 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PURI, PIER LORENZO, SACCO, ALESSANDRA · 2020 to 2025
$3.1M
Denervation activated super-enhancers of pathogenic IL6-STAT3 feedforward loop in FAPsR01AR076247 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PURI, PIER LORENZO · 2019 to 2023
$2.1M
Role of STAT3 in muscle stem cell activationR01AR064873 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI SACCO, ALESSANDRA · 2014 to 2018
$2.1M
Fbxw7 as a target to promote muscle stem cell expansionR21AR075205 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI SACCO, ALESSANDRA · 2019 to 2020
$472k
AFM-Téléthon (French Muscular Dystrophy Association) 21080NIAMS NIH HHS R01 AR056712NIAMS NIH HHS R01 AR064873NIAMS NIH HHS R01 AR076247NIAMS NIH HHS R01 AR077448NIAMS NIH HHS R21 AR075205U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) AR064873U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) AR075205U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) AR076247U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) AR077448
6 · The paper itself

Abstract

Skeletal muscle regeneration occurs through the finely timed activation of resident muscle stem cells (MuSC). Following injury, MuSC exit quiescence, undergo myogenic commitment, and regenerate the muscle. This process is coordinated by tissue microenvironment cues, however the underlying mechanisms regulating MuSC function are still poorly understood. Here, we demonstrate that the extracellular matrix protein Tenascin-C (TnC) promotes MuSC self-renewal and function. Mice lacking TnC exhibit reduced number of MuSC, and defects in MuSC self-renewal, myogenic commitment, and repair. We show that fibro-adipogenic progenitors are the primary cellular source of TnC during regeneration, and that MuSC respond through the surface receptor Annexin A2. We further demonstrate that TnC declines during aging, leading to impaired MuSC function. Aged MuSC exposed to soluble TnC show a rescued ability to both migrate and self-renew in vitro. Overall, our results highlight the pivotal role of TnC during muscle repair in healthy and aging muscle.

Indexed as

Adult Stem CellsAnnexin A2Muscle, SkeletalTenascinAnimalsMiceMice, KnockoutMuscle DevelopmentRegenerationAnnexin A2TenascinTnc protein, mouse

Identifiers

PMID41350439
PMCPMC12680774

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.