Evidence map›Paper›PMID 30201383›Full record

ReviewProgress in retinal and eye research2019

The peripheral eye: A neurogenic area with potential to treat retinal pathologies?

Marta Fernández-Nogales, Verónica Murcia-Belmonte, Holly Yu Chen, Eloísa Herrera

Open access · greenAbstract readReview
In one paragraph

Review in Progress in retinal and eye research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Development of the Binocular Circuit.Annual review of neuroscience · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Cell Fate of Retinal Progenitor Cells: In Ovo UbC-StarTrack Analysis.International journal of molecular sciences · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Loss of Active Neurogenesis in the Adult Shark Retina.Frontiers in cell and developmental biology · 2021
    Article
  12. Article
  13. Review
  14. Review
  15. 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

4 authors at 2 institutions in 2 countries.

Marta Fernández-NogalesInstituto de Neurociencias (CSIC-UMH), Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández, Campus San Juan, Av. Ramón y Cajal s/n, Alicante, 03550, Spain.
Verónica Murcia-BelmonteInstituto de Neurociencias (CSIC-UMH), Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández, Campus San Juan, Av. Ramón y Cajal s/n, Alicante, 03550, Spain.
Holly Yu ChenNeurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, MD, USA.
Eloísa HerreraInstituto de Neurociencias (CSIC-UMH), Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández, Campus San Juan, Av. Ramón y Cajal s/n, Alicante, 03550, Spain. Electronic address: e.herrera@umh.es.
Consejo Superior de Investigaciones Científicas · ESNational Institutes of Health · US

Funding

Regulation of retinal developmentZIAEY000450 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2025
$71.0M
Interventional approaches for restoring visionZIAEY000474 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2019
$15.5M
Regulation of gene expression in the retinaZ01EY000450 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2008 to 2008
$2.4M
Intramural NIH HHS Z01 EY000450Intramural NIH HHS ZIA EY000450Intramural NIH HHS ZIA EY000474
6 · The paper itself

Abstract

Numerous degenerative diseases affecting visual function, including glaucoma and retinitis pigmentosa, are produced by the loss of different types of retinal cells. Cell replacement therapy has emerged as a promising strategy for treating these and other retinal diseases. The retinal margin or ciliary body (CB) of mammals has been proposed as a potential source of cells to be used in degenerative conditions affecting the retina because it has been reported it might hold neurogenic potential beyond embryonic development. However, many aspects of the origin and biology of the CB are unknown and more recent experiments have challenged the capacity of CB cells to generate different types of retinal neurons. Here we review the most recent findings about the development of the marginal zone of the retina in different vertebrates and some of the mechanisms underlying the proliferative and neurogenic capacity of this fascinating region of the vertebrates eye. In addition, we performed experiments to isolate CB cells from the mouse retina, generated neurospheres and observed that they can be expanded with a proliferative ratio similar to neural stem cells. When induced to differentiate, cells derived from the CB neurospheres start to express early neural markers but, unlike embryonic stem cells, they are not able to fully differentiate in vitro or generate retinal organoids. Together with previous reports on the neurogenic capacity of CB cells, also reviewed here, our results contribute to the current knowledge about the potentiality of this peripheral region of the eye as a therapeutic source of functional retinal neurons in degenerative diseases.

Indexed as

AnimalsCell- and Tissue-Based TherapyCell Culture TechniquesCell DifferentiationCells, CulturedCiliary BodyHumansMiceNeurogenesisRetinal DegenerationCiliary bodyCiliary marginal zoneDevelopmentEye neurogenesisRetinaRetinal regeneration

Identifiers

PMID30201383
PMCPMC7654208
OpenAlexW2891102457

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.