Evidence map›Paper›PMID 34572321›Full record

ArticleBiomedicines2021

Derivation and Characterization of EGFP-Labeled Rabbit Limbal Mesenchymal Stem Cells and Their Potential for Research in Regenerative Ophthalmology.

Julia I Khorolskaya, Daria A Perepletchikova, Daniel V Kachkin, Kirill E Zhurenkov, Elga I Alexander-Sinkler, Julia S Ivanova, Natalia A Mikhailova, Miralda I Blinova

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 12 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

8 authors at 2 institutions in 1 country.

Julia I KhorolskayaInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.
Daria A PerepletchikovaInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.
Daniel V KachkinLaboratory of Amyloid Biology, St. Petersburg State University, 199034 St. Petersburg, Russia.ORCID 0000-0002-2279-8514
Kirill E ZhurenkovInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.ORCID 0000-0001-6270-2866
Elga I Alexander-SinklerInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.
Julia S IvanovaInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.
Natalia A MikhailovaInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.ORCID 0000-0003-1650-9330
Miralda I BlinovaInstitute of Cytology Russian Academy of Science, 194064 St. Petersburg, Russia.
Institute of Cytology · RUSt Petersburg University · RU

Funding

Russian Foundation of Basic Researc 19-34-90176Russian Foundation of Basic Research 19-34-90146Russian Foundation of Basic Research 19-34- 90153St. Petersburg State University 73024371The Ministry of Science and Higher Education Russian Federation 075-15-2020-773
6 · The paper itself

Abstract

The development of cell-based approaches to the treatment of various cornea pathologies, including limbal stem cell deficiency (LSCD), is an area of current interest in regenerative biomedicine. In this context, the shortage of donor material is urgent, and limbal mesenchymal stem cells (L-MSCs) may become a promising cell source for the development of these novel approaches, being established mainly within the rabbit model. In this study, we obtained and characterized rabbit L-MSCs and modified them with lentiviral transduction to express the green fluorescent protein EGFP (L-MSCs-EGFP). L-MSCs and L-MSCs-EGFP express not only stem cell markers specific for mesenchymal stem cells but also ABCG2, ABCB5, ALDH3A1, PAX6, and p63a specific for limbal epithelial stem cells (LESCs), as well as various cytokeratins (3/12, 15, 19). L-MSCs-EGFP have been proven to differentiate into adipogenic, osteogenic, and chondrogenic directions, as well as to transdifferentiate into epithelial cells. The possibility of using L-MSCs-EGFP to study the biocompatibility of various scaffolds developed to treat corneal pathologies was demonstrated. L-MSCs-EGFP may become a useful tool for studying regenerative processes occurring during the treatment of various corneal pathologies, including LSCD, with the use of cell-based technologies.

Indexed as

corneal regenerationEGFP-labeled cellslimbal mesenchymal stem cellslimbal stem cellsmesenchymal-epithelial transitionmesenchymal stem cellsregenerative medicine

Identifiers

PMID34572321
PMCPMC8465718
OpenAlexW3198104285

What OpenQuestion holds

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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.