Evidence map›Paper›PMID 17518629›Full record

ArticleTissue engineering2006

Structure and functional evaluation of tendon-skeletal muscle constructs engineered in vitro.

Lisa M Larkin, Sarah Calve, Tatiana Y Kostrominova, Ellen M Arruda

Abstract read
In one paragraph

Article in Tissue engineering, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

  1. Myotendinous Junction development and repair.Journal of orthopaedic translation · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Available In Vitro Models for Human Satellite Cells from Skeletal Muscle.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Review
  13. Review
  14. Bioinspired Scaffold Designs for Regenerating Musculoskeletal Tissue Interfaces.Regenerative engineering and translational medicine · 2020
    Article
  15. Article
  16. Using tools in mechanobiology to repair tendons.Current tissue microenvironment reports · 2020
    Article
  17. Article
  18. Review
  19. Review
  20. Biologics and stem cell-based therapies for rotator cuff repair.Annals of the New York Academy of Sciences · 2019
    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

4 authors.

Lisa M LarkinDepartment of Biomedical Engineering, Division of Geriatric Medicine, Muscle Mechanics Laboratory, University of Michigan, Ann Arbor, Michigan 48109, USA.
Sarah Calve
Tatiana Y Kostrominova
Ellen M Arruda

Funding

Electromechanical Stimuli on the Development of Engineered Myotendinous JunctionR21AR054359 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LARKIN, LISA M · 2007 to 2008
$343k
NIAMS NIH HHS R21 AR054359
6 · The paper itself

Abstract

During muscle contraction, the integrity of the myotendinous junction (MTJ) is important for the transmission of force from muscle to tendon. We evaluated the contractile and structural characteristics of 3-dimensional (3-D) skeletal muscle constructs co-cultured with engineered self-organized tendon constructs (n = 4), or segments of adult (n = 4) or fetal (n = 5) rat-tail tendon. We hypothesized that the co-culture of tendon and muscle would produce constructs with viable muscle-tendon interfaces that remain intact during generation of force. Construct diameter (lm) and maximum isometric force (microN) were measured, and specific force (kPa) was determined. After measure of force, constructs were loaded at a constant strain rate until failure and surface strains were recorded optically across the tendon, the muscle and the interface and used to determine the tangent modulus (passive stiffness) of the construct. Frozen samples were used for Trichrome Masson staining and immunofluorescent analysis of the MTJ-specific protein paxillin. No differences were observed between the groups with respect to diameter, maximum force, or specific force. The MTJ was robust and withstood tensile loading beyond the physiological strain range. The majority of the constructs failed in the muscle region. At the MTJ, there is an increase in the expression and localization of paxillin. In conclusion, using 3 sources of tendon tissue, we successfully engineered 3-D muscle-tendon constructs with functionally viable MTJ, characterized by structural features and protein expression patterns resembling neonatal MTJs in vivo.

Indexed as

Tissue EngineeringAnimalsCells, CulturedCulture MediaFemaleImmunohistochemistryIsometric ContractionMuscle, SkeletalOrgan Culture TechniquesPaxillinRatsRats, Inbred F344TendonsTensile StrengthCulture MediaPaxillin

Identifiers

PMID17518629
PMCPMC2798802

What OpenQuestion holds

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Read underepoch 390

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.