Evidence map›Paper›PMID 28979193›Full record

ArticleFrontiers in cellular neuroscience2017

Intraocular Injection of ES Cell-Derived Neural Progenitors Improve Visual Function in Retinal Ganglion Cell-Depleted Mouse Models.

Mundackal S Divya, Vazhanthodi A Rasheed, Tiffany Schmidt, Soundararajan Lalitha, Samer Hattar, Jackson James

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. The neuroimmune interface in retinal regeneration.Progress in retinal and eye research · 2025
    Review
  7. Article
  8. Review
  9. Optic nerve regeneration: Potential treatment approaches.Current opinion in pharmacology · 2024
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
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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

6 authors at 2 institutions in 2 countries.

Mundackal S DivyaNeuro-Stem Cell Biology Laboratory, Neurobiology Division, Rajiv Gandhi Centre for BiotechnologyThiruvananthapuram, India.
Vazhanthodi A RasheedNeuro-Stem Cell Biology Laboratory, Neurobiology Division, Rajiv Gandhi Centre for BiotechnologyThiruvananthapuram, India.
Tiffany SchmidtDepartment of Biology, Johns Hopkins UniversityBaltimore, MD, United States.
Soundararajan LalithaNeuro-Stem Cell Biology Laboratory, Neurobiology Division, Rajiv Gandhi Centre for BiotechnologyThiruvananthapuram, India.
Samer HattarDepartment of Biology, Johns Hopkins UniversityBaltimore, MD, United States.
Jackson JamesNeuro-Stem Cell Biology Laboratory, Neurobiology Division, Rajiv Gandhi Centre for BiotechnologyThiruvananthapuram, India.
Rajiv Gandhi Centre for Biotechnology · INJohns Hopkins University · US

Funding

Section on Light and Circadian RhythmsZIAMH002964 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI HATTAR, SAMER · 2017 to 2025
$24.1M
Role of mammalian retinal photoreceptors in non-image-forming visual functionsR01GM076430 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ZHAO, HAIQING · 2005 to 2018
$4.8M
NIGMS NIH HHS R01 GM076430
6 · The paper itself

Abstract

Retinal ganglion cell (RGC) transplantation is a promising strategy to restore visual function resulting from irreversible RGC degeneration occurring in glaucoma or inherited optic neuropathies. We previously demonstrated FGF2 induced differentiation of mouse embryonic stem cells (ESC) to RGC lineage, capable of retinal ganglion cell layer (GCL) integration upon transplantation. Here, we evaluated possible improvement of visual function by transplantation of ES cell derived neural progenitors in RGC depleted glaucoma mice models. ESC derived neural progenitors (ES-NP) were transplanted into N-Methyl-D-Aspartate (NMDA) injected, RGC-ablated mouse models and a pre-clinical glaucoma mouse model (DBA/2J) having sustained higher intra ocular pressure (IOP). Visual acuity and functional integration was evaluated by behavioral experiments and immunohistochemistry, respectively. GFP-expressing ES-NPs transplanted in NMDA-injected RGC-depleted mice differentiated into RGC lineage and possibly integrating into GCL. An improvement in visual acuity was observed after 2 months of transplantation, when compared to the pre-transplantation values. Expression of c-Fos in the transplanted cells, upon light induction, further suggests functional integration into the host retinal circuitry. However, the transplanted cells did not send axonal projections into optic nerve. Transplantation experiments in DBA/2J mouse showed no significant improvement in visual functions, possibly due to both host and transplanted retinal cell death which could be due to an inherent high IOP. We showed that, ES NPs transplanted into the retina of RGC-ablated mouse models could survive, differentiate to RGC lineage, and possibly integrate into GCL to improve visual function. However, for the survival of transplanted cells in glaucoma, strategies to control the IOP are warranted.

Indexed as

embryonic stem cell derived neural progenitorsfunctional integrationglaucomaretinal ganglion cellstransplantation

Identifiers

PMID28979193
PMCPMC5611488
OpenAlexW2754493834

What OpenQuestion holds

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LicenceCC BY
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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.