Evidence map›Paper›PMID 31603905›Full record

ArticlePloS one2019

Extracellular matrix turnover and inflammation in chemically-induced TMJ arthritis mouse models.

Mallory Morel, Angela Ruscitto, Serhiy Pylawka, Gwendolyn Reeve, Mildred C Embree

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. BoNT Injection into Temporomandibular Joint Alleviates TMJ Pain in Forced Mouth Opening Mouse Model.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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  8. Review
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  12. The temporomandibular joints disorders in patients with osteoporosis.Journal of oral and maxillofacial pathology : JOMFP
    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

5 authors at 2 institutions in 1 country.

Mallory MorelTMJ Biology and Regenerative Medicine Laboratory, College of Dental Medicine, Columbia University Irving Medical Center, New York, NY, United States of America.
Angela RuscittoTMJ Biology and Regenerative Medicine Laboratory, College of Dental Medicine, Columbia University Irving Medical Center, New York, NY, United States of America.
Serhiy PylawkaTMJ Biology and Regenerative Medicine Laboratory, College of Dental Medicine, Columbia University Irving Medical Center, New York, NY, United States of America.
Gwendolyn ReeveDivision of Oral and Maxillofacial Surgery, New York Presbyterian Weill Cornell Medical Center, New York, NY, United States of America.
Mildred C EmbreeTMJ Biology and Regenerative Medicine Laboratory, College of Dental Medicine, Columbia University Irving Medical Center, New York, NY, United States of America.
Columbia University · USPenn Presbyterian Medical Center · US

Funding

Improvement of Animal Models for TMJ Stem Cell-Based RegenerationR01DE029068 · NIDCR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EMBREE, MILDRED CHRISTINE · 2019 to 2023
$3.6M
NIDCR Dentist Scientist K99:Improve TMJ Fibrocartilage Regeneration StrategiesR00DE022060 · NIDCR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EMBREE, MILDRED CHRISTINE · 2014 to 2018
$1.2M
NIDCR NIH HHS R00 DE022060NIDCR NIH HHS R01 DE029068
6 · The paper itself

Abstract

The temporomandibular joint (TMJ) is a fibrocartilaginous tissue critical for chewing and speaking. In patients with temporomandibular disorders (TMDs), permanent tissue loss can occur. Recapitulating the complexity of TMDs in animal models is difficult, yet critical for the advent of new therapies. Synovial fluid from diseased human samples revealed elevated levels of tumor necrosis factor alpha (TNF-alpha). Here, we propose to recapitulate these findings in mice by subjecting murine TMJs with TNF-alpha or CFA (Complete Freund's Adjuvant) in mandibular condyle explant cultures and by local delivery in vivo using TMJ intra-articular injections. Both TNF-alpha and CFA delivery to whole mandibular explants and in vivo increased extracellular matrix deposition and increased cartilage thickness, while TNF-alpha treated explants had increased expression of inflammatory cytokines and degradative enzymes. Moreover, the application of TNF-alpha or CFA in both models reduced cell number. CFA delivery in vivo caused soft tissue inflammation, including pannus formation. Our work provides two methods of chemically induced TMJ inflammatory arthritis through a condyle explant model and intra-articular injection model that replicate findings seen in synovial fluid of human patients, which can be used for further studies delineating the mechanisms underlying TMJ pathology.

Indexed as

ADAMTS5 ProteinAdolescentAdultAgedAnimalsArthritis, ExperimentalCartilage, ArticularCollagen Type IICollagen Type XDisease Models, AnimalExtracellular MatrixFemaleFreund's AdjuvantGene ExpressionHumansInterleukinsADAMTS5 ProteinAdamts5 protein, mouseCol10a1 protein, mouseCol2a1 protein, mouseCollagen Type IICollagen Type XFreund's AdjuvantInterleukinsTumor Necrosis Factor-alpha

Identifiers

PMID31603905
PMCPMC6788689
OpenAlexW2979466589

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.