Evidence map›Paper›PMID 32723825›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

The optic nerve lamina region is a neural progenitor cell niche.

S L Bernstein, Y Guo, C Kerr, R J Fawcett, J H Stern, S Temple, Z Mehrabian

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. 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
1.7field-weighted citation impact, top 18% 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.

  1. Article
  2. Article
  3. Hopx(+) optic nerve head-astrocytes counter neuronal stress and glaucoma damage.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Considerations and implications of currentFrontiers in cell and developmental biology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. The neurosphere assay: an effectiveNeural regeneration research · 2021
    Article
  11. Article
  12. Review
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

7 authors at 3 institutions in 1 country.

S L BernsteinDepartment of Ophthalmology and Visual Sciences, University of Maryland School of Medicine, Baltimore, MD 21201; sbernstein@som.umaryland.edu.ORCID 0000-0001-7758-0136
Y GuoDepartment of Ophthalmology and Visual Sciences, University of Maryland School of Medicine, Baltimore, MD 21201.
C KerrDivision of Aging Biology, National Institutes of Health, Bethesda, MD 20892.
R J FawcettDepartment of Ophthalmology and Visual Sciences, University of Maryland School of Medicine, Baltimore, MD 21201.ORCID 0000-0001-8601-8268
J H SternAge-Related Macular Degeneration Program, Neural Stem Cell Institute, Rensselaer, NY 12144.
S TempleAge-Related Macular Degeneration Program, Neural Stem Cell Institute, Rensselaer, NY 12144.
Z MehrabianDepartment of Ophthalmology and Visual Sciences, University of Maryland School of Medicine, Baltimore, MD 21201.
University of Maryland, Baltimore · USNeural Stem Cell Institute · USNational Institutes of Health · US

Funding

Mechanisms of Optic Nerve Stroke NeuroprotectionR01EY015304 · NEI · UNIVERSITY OF MARYLAND BALTIMORE · PI BERNSTEIN, STEVEN L · 2004 to 2018
$4.7M
Preclinical Analysis of Ischemic Optic Nerve TreatmentR01EY028193 · NEI · UNIVERSITY OF MARYLAND BALTIMORE · PI BERNSTEIN, STEVEN L, JOHNSON, MARY A · 2017 to 2019
$1.0M
Cryo Upgrade of UMB EM Core FacilityS10RR026870 · NCRR · UNIVERSITY OF MARYLAND BALTIMORE · PI HSIA, RU-CHING · 2010 to 2010
$421k
NCRR NIH HHS S10 RR026870NEI NIH HHS R01 EY015304
6 · The paper itself

Abstract

Retinal ganglion cell axons forming the optic nerve (ON) emerge unmyelinated from the eye and become myelinated after passage through the optic nerve lamina region (ONLR), a transitional area containing a vascular plexus. The ONLR has a number of unusual characteristics: it inhibits intraocular myelination, enables postnatal ON myelination of growing axons, modulates the fluid pressure differences between eye and brain, and is the primary lesion site in the age-related disease open angle glaucoma (OAG). We demonstrate that the human and rodent ONLR possesses a mitotically active, age-depletable neural progenitor cell (NPC) niche, with unique characteristics and culture requirements. These NPCs generate both forms of macroglia: astrocytes and oligodendrocytes, and can form neurospheres in culture. Using reporter mice with SOX2-driven, inducible gene expression, we show that ONLR-NPCs generate macroglial cells for the anterior ON. Early ONLR-NPC loss results in regional dysfunction and hypomyelination. In adulthood, ONLR-NPCs may enable glial replacement and remyelination. ONLR-NPC depletion may help explain why ON diseases such as OAG progress in severity during aging.

Indexed as

Stem Cell NicheAnimalsAstrocytesAxonsCell DifferentiationGlaucoma, Open-AngleHumansMiceMyelin SheathNeurogliaNeuronsOligodendrogliaOptic NerveSOXB1 Transcription FactorsStem CellsSox2 protein, mouseSOXB1 Transcription Factorseyelaminaneural progenitor cell nicheoptic nervepostnatal axon growth

Identifiers

PMID32723825
PMCPMC7431091
OpenAlexW3046091102

What OpenQuestion holds

Textmetadata
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.