Evidence map›Paper›PMID 36158210›Full record

ArticleFrontiers in cell and developmental biology2022

Craniofacial tendon development-Characterization of extracellular matrix morphology and spatiotemporal protein distribution.

Stefanie H Korntner, Aniket Jana, Elizabeth Kinnard, Emily Leo, Timothy Beane, Xianmu Li, Rohit Sengupta, Lauren Becker, Catherine K Kuo

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Embryo movement is required for limb tendon maturation.Frontiers in cell and developmental biology · 2024
    Article
  4. Recombinant lysyl oxidase effects on embryonic tendon cell phenotype and behavior.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  5. 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

9 authors.

Stefanie H KorntnerFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Aniket JanaFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Elizabeth KinnardFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Emily LeoFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Timothy BeaneDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Xianmu LiDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Rohit SenguptaFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Lauren BeckerFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Catherine K KuoFischell Department of Bioengineering, University of Maryland, College Park, MD, United States.

Funding

Tendon Tissue Engineering Informed by Lysyl Oxidase Regulation of Embryonic Tendon Mechanical PropertiesR01AR072886 · NIAMS · UNIV OF MARYLAND, COLLEGE PARK · PI KUO, CATHERINE K. · 2017 to 2021
$1.4M
NIAMS NIH HHS R01 AR072886
6 · The paper itself

Abstract

Craniofacial (CF) tendons are often affected by traumatic injuries and painful disorders that can severely compromise critical jaw functions, such as mastication and talking. Unfortunately, tendons lack the ability to regenerate, and there are no solutions to restore their native properties or function. An understanding of jaw tendon development could inform tendon regeneration strategies to restore jaw function, however CF tendon development has been relatively unexplored. Using the chick embryo, we identified the jaw-closing Tendon of the musculus Adductor Mandibulae Externus (TmAM) and the jaw-opening Tendon of the musculus Depressor Mandibulae (TmDM) that have similar functions to the masticatory tendons in humans. Using histological and immunohistochemical (IHC) analyses, we characterized the TmAM and TmDM on the basis of cell and extracellular matrix (ECM) morphology and spatiotemporal protein distribution from early to late embryonic development. The TmAM and TmDM were detectable as early as embryonic day (d) 9 based on histological staining and tenascin-C (TNC) protein distribution. Collagen content increased and became more organized, cell density decreased, and cell nuclei elongated over time during development in both the TmAM and TmDM. The TmAM and TmDM exhibited similar spatiotemporal patterns for collagen type III (COL3), but differential spatiotemporal patterns for TNC, lysyl oxidase (LOX), and matrix metalloproteinases (MMPs). Our results demonstrate markers that play a role in limb tendon formation are also present in jaw tendons during embryonic development, implicate COL3, TNC, LOX, MMP2, and MMP9 in jaw tendon development, and suggest TmAM and TmDM possess different developmental programs. Taken together, our study suggests the chick embryo may be used as a model with which to study CF tendon extracellular matrix development, the results of which could ultimately inform therapeutic approaches for CF tendon injuries and disorders.

Indexed as

chick embryocollagencraniofacialjawlysyl oxidasematrix metalloproteinasetendontendon development

Identifiers

PMID36158210
PMCPMC9490420

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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.