Evidence map›Paper›PMID 37175400›Full record

ArticleInternational journal of molecular sciences2023

Embryonic Stem Cells Can Generate Oral Epithelia under Matrix Instruction.

Ridhima Das, Lisa Harper, Kayoko Kitajima, Tarig Al-Hadi Osman, Mihaela Roxana Cimpan, Anne Chr Johannssen, Salwa Suliman, Ian C Mackenzie, Daniela-Elena Costea

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Ridhima DasGade Laboratory for Pathology and Center for Cancer Biomarkers CCBIO, Institute for Clinical Medicine, University of Bergen, 5020 Bergen, Norway.
Lisa HarperInstitute for Cell and Molecular Science, Queen Mary University of London, London E1 4NS, UK.
Kayoko KitajimaDepartment of Endodontics, The Nippon Dental University School of Life Dentistry at Niigata, Niigata 951-8580, Japan.
Tarig Al-Hadi OsmanDepartment of Clinical Dentistry, University of Bergen, 5020 Bergen, Norway.
Mihaela Roxana CimpanDepartment of Clinical Dentistry, University of Bergen, 5020 Bergen, Norway.
Anne Chr JohannssenGade Laboratory for Pathology and Center for Cancer Biomarkers CCBIO, Institute for Clinical Medicine, University of Bergen, 5020 Bergen, Norway.
Salwa SulimanDepartment of Clinical Dentistry, University of Bergen, 5020 Bergen, Norway.
Ian C MackenzieInstitute for Cell and Molecular Science, Queen Mary University of London, London E1 4NS, UK.
Daniela-Elena CosteaGade Laboratory for Pathology and Center for Cancer Biomarkers CCBIO, Institute for Clinical Medicine, University of Bergen, 5020 Bergen, Norway.ORCID 0000-0001-7673-0358

Funding

The Norwegian Agency for International Cooperation and Quality Enhancement in Higher Education CPEA-LT-2016/10106).The Research Council of Norway 22325Western Norway Regional Health Authority 912260/2019
6 · The paper itself

Abstract

We aimed to investigate whether molecular clues from the extracellular matrix (ECM) can induce oral epithelial differentiation of pluripotent stem cells. Mouse embryonic stem cells (ESC) of the feeder-independent cell line E14 were used as a model for pluripotent stem cells. They were first grown in 2D on various matrices in media containing vitamin C and without leukemia inhibitory factor (LIF). Matrices investigated were gelatin, laminin, and extracellular matrices (ECM) synthesized by primary normal oral fibroblasts and keratinocytes in culture. Differentiation into epithelial lineages was assessed by light microscopy, immunocytochemistry, and flow cytometry for cytokeratins and stem cell markers. ESC grown in 2D on various matrices were afterwards grown in 3D organotypic cultures with or without oral fibroblasts in the collagen matrix and examined histologically and by immunohistochemistry for epithelial (keratin pairs 1/10 and 4/13 to distinguish epidermal from oral epithelia and keratins 8,18,19 to phenotype simple epithelia) and mesenchymal (vimentin) phenotypes. ECM synthesized by either oral fibroblasts or keratinocytes was able to induce, in 2D cultures, the expression of cytokeratins of the stratified epithelial phenotype. When grown in 3D, all ESC developed into two morphologically distinct cell populations on collagen gels: (i) epithelial-like cells organized in islands with occasional cyst- or duct-like structures and (ii) spindle-shaped cells suggestive of mesenchymal differentiation. The 3D culture on oral fibroblast-populated collagen matrices was necessary for further differentiation into oral epithelia. Only ESC initially grown on 2D keratinocyte or fibroblast-synthesized matrices reached full epithelial maturation. In conclusion, ESC can generate oral epithelia under matrix instruction.

Indexed as

CollagenKeratinocytesAnimalsCell DifferentiationCells, CulturedEmbryonic Stem CellsEpitheliumExtracellular MatrixFibroblastsKeratinsMiceCollagenKeratinsdifferentiationembryonic stem cellsfibroblastmatrixmousenicheoral mucosaskin

Identifiers

PMID37175400
PMCPMC10177836

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Registered trials

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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.