Evidence map›Paper›PMID 20934971›Full record

ArticleThe American journal of pathology2010

Relaxin regulates MMP expression and promotes satellite cell mobilization during muscle healing in both young and aged mice.

Xiaodong Mu, Maria L Urso, Kiley Murray, Freddie Fu, Yong Li

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Relaxin-2: Shaping the Proteomic Landscape of Skeletal Muscle Physiology, Glucose Trafficking, and Mitochondrial Function in Rat.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  2. Article
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  5. Review
  6. Article
  7. Article
  8. Article
  9. Matrix Metalloproteinase 13 from Satellite Cells is Required for Efficient Muscle Growth and Regeneration.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Anti-fibrotic actions of relaxin.British journal of pharmacology · 2017
    Review
  15. Review
  16. Article
  17. Observational
  18. Article
  19. Serum and tissue biomarkers in aortic stenosis.Global cardiology science & practice · 2015
    Article
  20. 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

5 authors at 3 institutions in 1 country.

Xiaodong MuLaboratory of Molecular Pathology Stem Cell Research Center (SCRC), Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Office 217, Bridgeside Point II, 450 Technology Drive Pittsburgh, PA 15219, USA.
Maria L Urso
Kiley Murray
Freddie Fu
Yong Li
University of Pittsburgh · USChildren's Hospital of Pittsburgh · USU.S. Army Research Institute of Environmental Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The polypeptide hormone relaxin has been proven to be effective in promoting both the remodeling and regeneration of various tissues, including cardiac muscle. In addition, our previous study demonstrated that relaxin is beneficial to skeletal muscle healing by both promoting muscle regeneration and preventing fibrosis formation. However, the molecular and cellular mechanisms of relaxin in regulating both myogenic cell differentiation and muscle healing process are still unclear. In this study, C2C12 mouse myoblasts and primary human myoblasts were treated with relaxin to investigate its potential effect in vitro; relaxin was also injected intramuscularly into the injured site of the mouse on the second day after injury to observe its function in vivo, especially in the aged muscle. Results showed that relaxin promoted myogenic differentiation, migration, and activation of matrix metalloproteinases (MMPs) of cultured myoblasts in vitro. In the injured muscle, relaxin administration promoted the activation of Pax7-positive skeletal muscle satellite cells and increased its local population compared with nontreated control muscles. Meanwhile, both angiogenesis and revascularization were increased, while the extended inflammatory reaction was repressed in the relaxin-treated injured muscle. Moreover, relaxin similarly promoted muscle healing in mice with aged muscle. These results revealed the multiple effects of relaxin in systematically improving muscle healing as well as its potential for clinical applications in patients with skeletal muscle injuries and diseases.

Indexed as

AgingAnimalsCell LineCell MovementCyclin-Dependent Kinase Inhibitor p21Enzyme ActivationHumansIsoenzymesMaleMatrix MetalloproteinasesMiceMice, Inbred C57BLMuscle, SkeletalNeovascularization, PhysiologicPAX7 Transcription FactorRegenerationCyclin-Dependent Kinase Inhibitor p21IsoenzymesMatrix MetalloproteinasesPAX7 Transcription FactorRelaxin

Identifiers

PMID20934971
PMCPMC2966798
OpenAlexW1979052871

What OpenQuestion holds

Textmetadata
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.