Evidence map›Paper›PMID 28129848›Full record

ReviewMethods in cell biology2017

Using the zebrafish to understand tendon development and repair.

J W Chen, J L Galloway

Abstract readReview
In one paragraph

Review in Methods in cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
8.6field-weighted citation impact, top 3% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Zebrafish: An Emerging Model for Orthopedic Research.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2020
    Review
  4. Zebrafish models of sarcopenia.Disease models & mechanisms · 2020
    Review
  5. Review
  6. Scleraxis genes are required for normal musculoskeletal development and for rib growth and mineralization in zebrafish.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  7. 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

2 authors at 2 institutions in 1 country.

J W ChenMassachusetts General Hospital, Boston, MA, United States; Harvard Medical School, Boston, MA, United States.
J L GallowayMassachusetts General Hospital, Boston, MA, United States; Harvard Medical School, Boston, MA, United States.
Harvard University · USMassachusetts General Hospital · US

Funding

The Roles of BMP Genes and Morphogenesis of the Appendicular and Dermal SkeletonsP01DK056246 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI DEMAY, MARIE, KRONENBERG, HENRY M. · 1999 to 2015
$19.3M
The reprogramming of limb progenitor cellsR01HD032443 · NICHD · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI CLIFFORD J. TABIN · 1995 to 2026
$4.6M
Genetic and chemical screening in zebrafish to study tendon developmentR00HD069533 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI GALLOWAY, JENNA L · 2013 to 2015
$677k
The origin and function of tendon progenitors in craniofacial morphogenesis and patterningR03DE024771 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI GALLOWAY, JENNA L · 2015 to 2016
$261k
Genetic and chemical screening in zebrafish to study tendon developmentK99HD069533 · NICHD · HARVARD MEDICAL SCHOOL · PI GALLOWAY, JENNA L · 2011 to 2012
$178k
NICHD NIH HHS K99 HD069533NICHD NIH HHS R00 HD069533NICHD NIH HHS R01 HD032443NIDCR NIH HHS R03 DE024771NIDDK NIH HHS P01 DK056246
6 · The paper itself

Abstract

Tendons are important components of our musculoskeletal system. Injuries to these tissues are very common, resulting from occupational-related injuries, sports-related trauma, and age-related degeneration. Unfortunately, there are few treatment options, and current therapies rarely restore injured tendons to their original function. An improved understanding of the pathways regulating their development and repair would have significant impact in stimulating the formulation of regenerative-based approaches for tendon injury. The zebrafish provides an ideal system in which to perform genetic and chemical screens to identify new pathways involved in tendon biology. Until recently, there had been few descriptions of tendons and ligaments in the zebrafish and their similarity to mammalian tendon tissues. In this chapter, we describe the development of the zebrafish tendon and ligament tissues in the context of their gene expression, structure, and interactions with neighboring musculoskeletal tissues. We highlight the similarities with tendon development in higher vertebrates, showing that the craniofacial tendons and ligaments in zebrafish morphologically, molecularly, and structurally resemble mammalian tendons and ligaments from embryonic to adult stages. We detail methods for fluorescent in situ hybridization and immunohistochemistry as an assay to examine morphological changes in the zebrafish musculoskeleton. Staining assays such as these could provide the foundation for screen-based approaches to identify new regulators of tendon development, morphogenesis, and repair. These discoveries would provide new targets and pathways to study in the context of regenerative medicine-based approaches to improve tendon healing.

Indexed as

AnimalsCell DifferentiationDisease Models, AnimalHumansIn Situ Hybridization, FluorescenceLigamentsMorphogenesisRegenerationRegenerative MedicineTendon InjuriesTendonsWound HealingZebrafishFluorescent in situ hybridizationImmunohistochemistryLigamentScleraxisTendonZebrafish

Identifiers

PMID28129848
PMCPMC5633932
OpenAlexW2552740148

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.