Evidence map›Paper›PMID 30389962›Full record

ArticleScientific reports2018

Human Wharton's jelly mesenchymal stem cells protect axotomized rat retinal ganglion cells via secretion of anti-inflammatory and neurotrophic factors.

Jose E Millán-Rivero, Francisco M Nadal-Nicolás, David García-Bernal, Paloma Sobrado-Calvo, Miguel Blanquer, Jose M Moraleda, Manuel Vidal-Sanz, Marta Agudo-Barriuso

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

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  7. Tissue Engineering and Ophthalmology.Turkish journal of ophthalmology · 2024
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  12. Mesenchymal stem cells for repairing glaucomatous optic nerve.International journal of ophthalmology · 2024
    Review
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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.

Jose E Millán-RiveroUnidad de Terapia Celular y Trasplante Hematopoyético. Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), Murcia, Spain.
Francisco M Nadal-NicolásDpto Oftalmología, Universidad de Murcia, Murcia, Spain.ORCID http://orcid.org/0000-0003-4121-514X
David García-BernalUnidad de Terapia Celular y Trasplante Hematopoyético. Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), Murcia, Spain.ORCID http://orcid.org/0000-0001-6610-8442
Paloma Sobrado-CalvoDpto Oftalmología, Universidad de Murcia, Murcia, Spain.
Miguel BlanquerUnidad de Terapia Celular y Trasplante Hematopoyético. Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), Murcia, Spain.
Jose M MoraledaUnidad de Terapia Celular y Trasplante Hematopoyético. Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), Murcia, Spain.
Manuel Vidal-SanzDpto Oftalmología, Universidad de Murcia, Murcia, Spain.
Marta Agudo-BarriusoDpto Oftalmología, Universidad de Murcia, Murcia, Spain. martabar@um.es.ORCID http://orcid.org/0000-0002-8566-9277

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cell (MSC) transplantation is emerging as an ideal tool to restore the wounded central nervous system (CNS). MSCs isolated from extra-embryonic tissues have some advantages compared to MSCs derived from adult ones, such as an improved proliferative capacity, life span, differentiation potential and immunomodulatory properties. In addition, they are more immunoprivileged, reducing the probability of being rejected by the recipient. Umbilical cords (UCs) are a good source of MSCs because they are abundant, safe, non-invasively harvested after birth and, importantly, they are not encumbered with ethical problems. Here we show that the intravitreal transplant of Wharton´s jelly mesenchymal stem cells isolated from three different human UCs (hWJMSCs) delays axotomy-induced retinal ganglion cell (RGC) loss. In vivo, hWJMSCs secrete anti-inflammatory molecules and trophic factors, the latter alone may account for the elicited neuroprotection. Interestingly, this expression profile differs between naive and injured retinas, suggesting that the environment in which the hWJMSCs are modulates their secretome. Finally, even though the transplant itself is not toxic for RGCs, it is not innocuous as it triggers a transient but massive infiltration of Iba1

Indexed as

AnimalsAnti-Inflammatory AgentsAxotomyDisease Models, AnimalFemaleHumansIntravitreal InjectionsMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNerve Growth FactorsRatsRats, Sprague-DawleyRetinal DegenerationRetinal Ganglion CellsTreatment OutcomeUmbilical CordAnti-Inflammatory AgentsNerve Growth Factors

Identifiers

PMID30389962
PMCPMC6214908

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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.