Evidence map›Paper›PMID 22983793›Full record

ArticleBiomedical microdevices2013

Fibroblasts influence muscle progenitor differentiation and alignment in contact independent and dependent manners in organized co-culture devices.

Nikhil Rao, Samantha Evans, Danique Stewart, Katrina H Spencer, Farah Sheikh, Elliot E Hui, Karen L Christman

Abstract read
In one paragraph

Article in Biomedical microdevices, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. A novel protocol for the direct isolation of a highly pure and regenerative population of satellite stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  5. MyoD Over-Expression Rescues GST-bFGF Repressed Myogenesis.International journal of molecular sciences · 2024
    Article
  6. Review
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  11. FGF/FGFR signaling in health and disease.Signal transduction and targeted therapy · 2020
    Review
  12. Neuromuscular disease modeling on a chip.Disease models & mechanisms · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Tissue engineering. Part A · 2017
    Article
  17. Article
  18. Article
  19. Patterning of sharp cellular interfaces with a reconfigurable elastic substrate.Integrative biology : quantitative biosciences from nano to macro · 2017
    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

7 authors at 4 institutions in 1 country.

Nikhil RaoDepartment of Bioengineering, University of California, San Diego. 2880 Torrey Pines Scenic Drive, La Jolla, CA 92037, USA.
Samantha Evans
Danique Stewart
Katrina H Spencer
Farah Sheikh
Elliot E Hui
Karen L Christman
University of California, Irvine · USUniversity of California, San Diego · USTorrey Pines Institute For Molecular Studies · USUniversity of California, Los Angeles · US

Funding

Training in Multi-Scale Analysis of Biological Structure and FunctionT32EB009380 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrew D. McCulloch, Padmini Rangamani · 2009 to 2026
$4.8M
The molecular mechanisms underlying arrhythmogenic right ventricular dysplasia/cardiomyopathyR01HL095780 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHEIKH, FARAH · 2009 to 2018
$3.9M
Integrative Bioengineering of Heart, Vessels, and BloodT32HL105373 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, INTAGLIETTA, MARCOS · 2010 to 2019
$3.6M
Engineering a Dynamic Extracellular Matrix MicroenvironmentDP2OD004309 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHRISTMAN, KAREN L · 2008 to 2009
$2.4M
Training Program in Systems Biology of DevelopmentT32HD060555 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2009 to 2013
$1.3M
Enhanced cardiomyocyte differentiation and maturation using myocardial matrixR21HL104493 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHRISTMAN, KAREN L, SHEIKH, FARAH · 2010 to 2011
$396k
NHLBI NIH HHS 1R21HL104493-01NHLBI NIH HHS R01 HL095780NHLBI NIH HHS R21 HL104493NIBIB NIH HHS T32 EB009380NIBIB NIH HHS T32EB009380-02NICHD NIH HHS T32 HD060555NICHD NIH HHS T32-HD060555NIH HHS 1-DP2-OD004309-01NIH HHS DP2 OD004309
6 · The paper itself

Abstract

Myoblasts are precursor muscle cells that lie nascent to mature skeletal muscle. Once muscle is damaged, these cells migrate, fuse, and regenerate the muscle tissue. It is known that skeletal muscle can partially regenerate in vivo after muscle tissue damage. However, this regeneration does not always occur, especially in more severe injuries. Cellular therapy using tissue-engineering approaches has been shown to improve organ repair and function. To exploit potential benefits of using cell therapy as an avenue for skeletal muscle repair, it is important to understand the cellular dynamics underlying skeletal myocyte formation and growth. Cardiac fibroblasts have been shown to have a major influence on cardiomyocyte function, repair, and overall spatial distribution. However, little is known regarding fibroblasts' role on skeletal myocyte function. In this study, we utilized a reconfigurable co-culture device to understand the contact and paracrine effects of fibroblasts on skeletal myocyte alignment and differentiation using murine myoblast and fibroblast cell lines. We demonstrate that myotube alignment is increased by direct contact with fibroblasts, while myotube differentiation is reduced both in the gap and contact configurations with fibroblasts after 6 days of co-culture. Furthermore, neutralizing antibodies to FGF-2 can block these effects of fibroblasts on myotube differentiation and alignment. Finally, bi-directional signaling is critical to the observed myoblast-fibroblast interactions, since conditioned media could not reproduce the same effects observed in the gap configuration. These findings could have direct implications on cell therapies for repairing skeletal muscle, which have only utilized skeletal myoblasts or stem cell populations alone.

Indexed as

Cell Differentiation3T3 CellsAnimalsCell CommunicationCoculture TechniquesFibroblast Growth Factor 2FibroblastsMiceMuscle CellsMuscle, SkeletalMyoblastsFibroblast Growth Factor 2

Identifiers

PMID22983793
PMCPMC3537877
OpenAlexW2094648414

What OpenQuestion holds

Textmetadata
LicenceTDM
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.