Evidence map›Paper›PMID 34192972›Full record

ArticleThe Annals of otology, rhinology, and laryngology2022

Preliminary Investigation of In vitro, Bidirectional Vocal Fold Muscle-Mucosa Interactions.

Rysouke Nakamura, Carina Doyle, Renjie Bing, Aaron M Johnson, Ryan C Branski

Open access · greenAbstract read
In one paragraph

Article in The Annals of otology, rhinology, and laryngology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

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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 1 institution in 1 country.

Rysouke NakamuraRehabilitation Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Carina DoyleRehabilitation Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Renjie BingRehabilitation Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Aaron M JohnsonOtolaryngology-Head and Neck Surgery, NYU Grossman School of Medicine, New York, NY, USA.ORCID https://orcid.org/0000-0002-7577-0267
Ryan C BranskiRehabilitation Medicine, NYU Grossman School of Medicine, New York, NY, USA.ORCID https://orcid.org/0000-0003-1190-9036
New York University · US

Funding

Multiple mechanisms underlying GR-mediated therapies for fibroplasia of the vocal foldsR01DC017397 · NIDCD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BRANSKI, RYAN COMFORT · 2018 to 2022
$2.6M
Optimal RNA-based therapeutics for vocal fold injury and fibrosisR01DC013277 · NIDCD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BRANSKI, RYAN COMFORT · 2014 to 2018
$2.3M
NIDCD NIH HHS R01 DC013277NIDCD NIH HHS R01 DC017397
6 · The paper itself

Abstract

objectiveOversimplified clinical dogma suggests that laryngeal diseases fall into two broad, mutually exclusive diagnostic categories-mucosal injury or neuromuscular/functional disorders. Extensive investigation in the lower airway as well as other organ systems suggest complex interactions between tissue types underlying both tissue health and pathological states. To date, no such relationship has been described in the vocal folds, likely the most bioactive organ in the body. We hypothesize interactions between the vocal fold muscle and mucosa likely contribute to aberrant phonatory physiology and warrant further investigation to ultimately develop novel therapeutic strategies.

methodsPrimary culture of myoblasts from rat thyroarytenoid muscle and fibroblasts from the vocal fold mucosa were established. Co-culture and conditioned media experiments were performed to established bidirectional interactions between cell types. Transforming Growth Factor (TGF)-β was employed to stimulate a fibrotic phenotype in culture. In addition to quantitative PCR, standard migration and proliferation assays were performed as well as immunocytochemistry.

resultsBidirectional cell-cell interactions were observed. Without TGF-β stimulation, myoblast conditioned media inhibited fibroblast migration, but enhanced proliferation. Conversely, fibroblast conditioned media increased both myoblast proliferation and migration. Myoblast conditioned media decreased TGF-β-mediated gene expression and of particular interest, ACTA2 mRNA expression. In both co-culture and in response to fibroblast conditioned media, myosin heavy chain (Myh2) mRNA expression decreased in myoblasts.

conclusionsThese data are the first to describe interactions between cell types within the vocal fold. The implications for these interactions in vivo warrant further investigation to develop and refine optimal treatment strategies.

Indexed as

FibroblastsVocal CordsAnimalsCulture Media, ConditionedHumansMusclesRatsRNA, MessengerTransforming Growth Factor betaCulture Media, ConditionedRNA, MessengerTransforming Growth Factor betafibroblastfibrosismyoblastvocal foldvoicevoice disorderwound healing

Identifiers

PMID34192972
PMCPMC11775648
OpenAlexW3173189741

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.