Evidence map›Paper›PMID 34205905›Full record

ArticleInternational journal of molecular sciences2021

Can Human Oral Mucosa Stem Cells Differentiate to Corneal Epithelia?

Sonia López, Lía Hoz, Eda Patricia Tenorio, Beatriz Buentello, Fátima Sofía Magaña, Ana Wintergerst, Alejandro Navas, Yonathan Garfias, Higinio Arzate

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
1.9field-weighted citation impact, top 14% 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, 19 citations in OpenAlex.

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  12. Synopsis of Barrier Function of Skin and Oral Mucosa-Volume 1.International journal of molecular sciences · 2021
    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 at 1 institution in 1 country.

Sonia LópezLaboratorio de Biología Periodontal, Facultad de Odontología, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.
Lía HozLaboratorio de Biología Periodontal, Facultad de Odontología, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.ORCID 0000-0002-8284-0745
Eda Patricia TenorioDepartamento de Bioquímica, Facultad de Medicina, UNAM, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.ORCID 0000-0002-4725-2286
Beatriz BuentelloInstituto de Oftalmología Conde de Valenciana, CDMX 06800, Mexico.ORCID 0000-0003-4529-990X
Fátima Sofía MagañaInstituto de Oftalmología Conde de Valenciana, CDMX 06800, Mexico.ORCID 0000-0002-1535-9898
Ana WintergerstLaboratorio de Biología Periodontal, Facultad de Odontología, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.
Alejandro NavasInstituto de Oftalmología Conde de Valenciana, CDMX 06800, Mexico.ORCID 0000-0002-9417-5711
Yonathan GarfiasDepartamento de Bioquímica, Facultad de Medicina, UNAM, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.
Higinio ArzateLaboratorio de Biología Periodontal, Facultad de Odontología, Universidad Nacional Autónoma de México, CDMX 04510, Mexico.ORCID 0000-0002-3735-4924
Universidad Nacional Autónoma de México · MX

Funding

Consejo Nacional de Ciencia y Tecnología 0311Universidad nacional Autónoma de México, DGAPA-PAPIIT IN203920Universidad Nacional Autónoma de México, DGAPA-PAPIIT: IN203821
6 · The paper itself

Abstract

Human oral mucosa stem cells (hOMSCs) arise from the neural crest, they can self-renew, proliferate, and differentiate to several cell lines and could represent a good source for application in tissue engineering. Because of their anatomical location, hOMSCs are easy to isolate, have multilineage differentiation capacity and express embryonic stem cells markers such as-Sox2, Oct3/4 and Nanog. We have used SHEM (supplemented hormonal epithelial medium) media and cultured hOMSCs over human amniotic membrane and determined the cell's capacity to differentiate to an epithelial-like phenotype and to express corneal specific epithelial markers-CK3, CK12, CK19, Pan-cadherin and E-cadherin. Our results showed that hOMSCs possess the capacity to attach to the amniotic membrane and express CK3, CK19, Pan-Cadherin and E-Cadherin without induction with SHEM media and expressed CK12 or changed the expression pattern of E-Cadherin to a punctual-like feature when treated with SHEM media. The results observed in this study show that hOMSCs possess the potential to differentiate toward epithelial cells. In conclusion, our results revealed that hOMSCs readily express markers for corneal determination and could provide the ophthalmology field with a therapeutic alternative for tissue engineering to achieve corneal replacement when compared with other techniques. Nevertheless, further studies are needed to develop a predictable therapeutic alternative for cornea replacement.

Indexed as

AmnionCell DifferentiationCells, CulturedCorneaCulture MediaEmbryonic Stem CellsEpithelial CellsEpithelium, CornealGene Expression Regulation, DevelopmentalHumansMesenchymal Stem CellsMouth MucosaTissue EngineeringCulture Mediacorneaepithelial differentiationoral mucosastem cells

Identifiers

PMID34205905
PMCPMC8198937
OpenAlexW3167343904

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.