Evidence map›Paper›PMID 32463804›Full record

ArticleJCI insight2020

Scleraxis is required for the growth of adult tendons in response to mechanical loading.

Jonathan P Gumucio, Martin M Schonk, Yalda A Kharaz, Eithne Comerford, Christopher L Mendias

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 70 citations in OpenAlex.

  1. A who's who of cell types in skeletal muscle.Communications biology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. The Secretome From Mechanically Loaded Myoblasts Enhances Tenocyte-Mediated Wound Healing in a 3D In Vitro Tendon Model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Article
  17. Article
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  20. Tendon mechanobiology in the context of tendon biofabrication.Frontiers in bioengineering and biotechnology · 2025
    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

5 authors at 3 institutions in 2 countries.

Jonathan P GumucioDepartment of Molecular & Integrative Physiology and.
Martin M SchonkHospital for Special Surgery, New York, New York, USA.
Yalda A KharazDepartment of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, and Medical Research Council Versus Arthritis Centre for Integrated Research into Musculoskeletal Ageing, University of Liverpool, Liverpool, United Kingdom.
Eithne ComerfordDepartment of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, and Medical Research Council Versus Arthritis Centre for Integrated Research into Musculoskeletal Ageing, University of Liverpool, Liverpool, United Kingdom.
Christopher L MendiasDepartment of Molecular & Integrative Physiology and.
Arthritis UK · GBHospital for Special Surgery · USUniversity of Michigan · US

Funding

Sex Differences in Tendon Growth and RemodelingR01AR063649 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RODEO, SCOTT A · 2013 to 2022
$3.6M
Fatty Macrophage Regulation of Atrophy and Inflammation in Rotator Cuff TearsF31AR065931 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUMUCIO, JONATHAN PAUL · 2014 to 2016
$103k
NIAMS NIH HHS F31 AR065931NIAMS NIH HHS R01 AR063649
6 · The paper itself

Abstract

Scleraxis is a basic helix-loop-helix transcription factor that plays a central role in promoting tenocyte proliferation and matrix synthesis during embryonic tendon development. However, the role of scleraxis in the growth and adaptation of adult tendons is not known. We hypothesized that scleraxis is required for tendon growth in response to mechanical loading and that scleraxis promotes the specification of progenitor cells into tenocytes. We conditionally deleted scleraxis in adult mice using a tamoxifen-inducible Cre-recombinase expressed from the Rosa26 locus (ScxΔ) and then induced tendon growth in Scx+ and ScxΔ adult mice via plantaris tendon mechanical overload. Compared with the WT Scx+ group, ScxΔ mice demonstrated blunted tendon growth. Transcriptional and proteomic analyses revealed significant reductions in cell proliferation, protein synthesis, and extracellular matrix genes and proteins. Our results indicate that scleraxis is required for mechanically stimulated adult tendon growth by causing the commitment of CD146+ pericytes into the tenogenic lineage and by promoting the initial expansion of newly committed tenocytes and the production of extracellular matrix proteins.

Indexed as

AnimalsCell DifferentiationCell ProliferationExtracellular MatrixMice, TransgenicMuscle, SkeletalProteomicsSignal TransductionStem CellsTendonsCell BiologyExtracellular matrixPericytesStem cells

Identifiers

PMID32463804
PMCPMC7406294
OpenAlexW3031225341

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.