Evidence map›Paper›PMID 33910192›Full record

ArticleCells, tissues, organs2021

Protein Substrate Alters Cell Physiology in Primary Culture of Vocal Fold Epithelial Cells.

Emily E Kimball, Lea Sayce, Xiaochuan C Xu, Chase M Kruszka, Bernard Rousseau

Open access · greenAbstract read
In one paragraph

Article in Cells, tissues, organs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 1 country.

Emily E KimballDepartment of Hearing and Speech Sciences, Vanderbilt University, Nashville, Tennessee, USA.
Lea SayceDepartment of Communication Sciences and Disorders, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Xiaochuan C XuDepartment of Communication Sciences and Disorders, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Chase M KruszkaDepartment of Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Bernard RousseauDepartment of Communication Sciences and Disorders, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
University of Pittsburgh · USVanderbilt University · USVanderbilt University Medical Center · US

Funding

Pre-Clinical Testing of the Safety and Efficacy of Treatments for Voice DisordersR01DC015405 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ROUSSEAU, BERNARD · 2016 to 2020
$2.8M
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
Development of a Patient-Specific Surgical Planning Tool for Type I LaryngoplastyR01DC016236 · NIDCD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COYLE, JAMES L · 2018 to 2022
$2.4M
NIDCD NIH HHS R01 DC015405NIDCD NIH HHS R01 DC016236NIDCD NIH HHS R01 DC017397
6 · The paper itself

Abstract

The basement membrane interacts directly with the vocal fold epithelium. Signaling between the basement membrane and the epithelium modulates gene regulation, differentiation, and proliferation. The purpose of this study was to identify an appropriate simple single-protein substrate for growth of rabbit vocal fold epithelial cells. Vocal folds from 3 New Zealand white rabbits (Oryctolagus cuniculus) were treated to isolate epithelial cells, and cells were seeded onto cell culture inserts coated with collagen I, collagen IV, laminin, or fibronectin. Transepithelial electrical resistance (TEER) was measured, and phase contrast microscopy, PanCK, CK14, and E-cadherin immunofluorescence were utilized to assess for epithelial cell-type characteristics. Further investigation via immunofluorescence labeling was conducted to assess proliferation (Ki67) and differentiation (Vimentin). There was a significant main effect of substrate on TEER, with collagen IV eliciting the highest, and laminin the lowest resistance. Assessment of relative TEER across cell lines identified a larger range of TEER in collagen I and laminin. Phase contrast imaging identified altered morphology in the laminin condition, but cell layer depth did not appear to be related to TEER, differentiation, or morphology. Ki67 staining additionally showed no significant difference in proliferation. All conditions had confluent epithelial cells and dispersed mesenchymal cells, with increased mesenchymal cell numbers over time; however, a higher proportion of mesenchymal cells was observed in the laminin condition. The results suggest collagen IV is a preferable basement membrane substrate for in vitro vocal fold epithelial primary cell culture, providing consistent TEER and characteristic cell morphology, and that laminin is an unsuitable substrate for vocal fold epithelial cells and may promote mesenchymal cell proliferation.

Indexed as

Epithelial CellsVocal CordsAnimalsBasement MembraneCell AdhesionCell CountCells, CulturedCollagen Type IVLamininRabbitsCollagen Type IVLamininBasement membraneCell cultureCulture substrateEpitheliumVocal fold

Identifiers

PMID33910192
PMCPMC8222167
OpenAlexW3159799770

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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.