Evidence map›Paper›PMID 23555841›Full record

ArticlePloS one2013

The paratenon contributes to scleraxis-expressing cells during patellar tendon healing.

Nathaniel A Dyment, Chia-Feng Liu, Namdar Kazemi, Lindsey E Aschbacher-Smith, Keith Kenter, Andrew P Breidenbach, Jason T Shearn, Christopher Wylie, David W Rowe, David L Butler

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
5.5field-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

97 citing papers in PubMed, 167 citations in OpenAlex.

  1. Article
  2. PIEZO1 Is a Contextual Mechanosensor and Its Depletion in Scx-Lineage Cells Accelerates Structural and Functional Recovery.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Prolyl-Hydroxyproline Promotes Structural Matrix Organization in 3D Equine Tendon Proper and Peritenon Post-Injury Model.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  4. Loss of type III collagen has limited effect on tendon healing in young adult mice.Matrix biology : journal of the International Society for Matrix Biology · 2026
    Article
  5. Review
  6. Collagen III Deficiency Following Injury in Female Murine Tendons Alters Matrix Composition, Structure, Organization and Function.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  7. Grafts in tendon repair.Materials today. Bio · 2026
    Review
  8. 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
  9. Article
  10. Article
  11. Comparative Analysis of Tendon Healing in a Clinically Relevant Mouse Model of Achilles Tendon Repair.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

37 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

10 authors at 4 institutions in 1 country.

Nathaniel A DymentDepartment of Reconstructive Sciences, College of Dental Medicine, University of Connecticut Health Center, Farmington, Connecticut, United States of America. dyment@uchc.edu
Chia-Feng Liu
Namdar Kazemi
Lindsey E Aschbacher-Smith
Keith Kenter
Andrew P Breidenbach
Jason T Shearn
Christopher Wylie
David W Rowe
David L Butler
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · USUConn Health · USUniversity of Cincinnati Medical Center · US

Funding

Skeletal, Craniofacial and Oral Biology Training GrantT90DE021989 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MINA, MINA · 2011 to 2022
$4.5M
In Vitro Mechanical Stimulation to Enhance Tendon RepairR01AR046574 · NIAMS · UNIVERSITY OF CINCINNATI · PI BUTLER, DAVID L · 2000 to 2009
$3.5M
A Developmentally-Based Tissue Engineering Approach to Improve Tendon RepairR01AR056943 · NIAMS · UNIVERSITY OF CINCINNATI · PI SHEARN, JASON T · 2009 to 2013
$3.3M
Assessing lineage decisions of musculoskeletal progenitor cells with agingR01AR054713 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ROWE, DAVID W. · 2006 to 2010
$2.0M
NIAMS NIH HHS AR054713-05NIAMS NIH HHS AR46574-10NIAMS NIH HHS AR56943-03NIAMS NIH HHS R01 AR046574NIAMS NIH HHS R01 AR054713NIAMS NIH HHS R01 AR056943NIDCR NIH HHS 5T90DE021989-01NIDCR NIH HHS T90 DE021989
6 · The paper itself

Abstract

The origin of cells that contribute to tendon healing, specifically extrinsic epitenon/paratenon cells vs. internal tendon fibroblasts, is still debated. The purpose of this study is to determine the location and phenotype of cells that contribute to healing of a central patellar tendon defect injury in the mouse. Normal adult patellar tendon consists of scleraxis-expressing (Scx) tendon fibroblasts situated among aligned collagen fibrils. The tendon body is surrounded by paratenon, which consists of a thin layer of cells that do not express Scx and collagen fibers oriented circumferentially around the tendon. At 3 days following injury, the paratenon thickens as cells within the paratenon proliferate and begin producing tenascin-C and fibromodulin. These cells migrate toward the defect site and express scleraxis and smooth muscle actin alpha by day 7. The thickened paratenon tissue eventually bridges the tendon defect by day 14. Similarly, cells within the periphery of the adjacent tendon struts express these markers and become disorganized. Cells within the defect region show increased expression of fibrillar collagens (Col1a1 and Col3a1) but decreased expression of tenogenic transcription factors (scleraxis and mohawk homeobox) and collagen assembly genes (fibromodulin and decorin). By contrast, early growth response 1 and 2 are upregulated in these tissues along with tenascin-C. These results suggest that paratenon cells, which normally do not express Scx, respond to injury by turning on Scx and assembling matrix to bridge the defect. Future studies are needed to determine the signaling pathways that drive these cells and whether they are capable of producing a functional tendon matrix. Understanding this process may guide tissue engineering strategies in the future by stimulating these cells to improve tendon repair.

Indexed as

Gene Expression RegulationActinsAnimalsBasic Helix-Loop-Helix ProteinsCell MovementCollagenExtracellular Matrix ProteinsFibromodulinGreen Fluorescent ProteinsImmunohistochemistryMiceMuscle, SmoothPatellar LigamentPhenotypePrincipal Component AnalysisProteoglycansActinsBasic Helix-Loop-Helix ProteinsCollagenExtracellular Matrix ProteinsFibromodulinFmod protein, mouseGreen Fluorescent ProteinsProteoglycansScx protein, mouseTenascin

Identifiers

PMID23555841
PMCPMC3608582
OpenAlexW1972137150

What OpenQuestion holds

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Registered trials

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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.