Evidence map›Paper›PMID 29782826›Full record

ArticleExperimental eye research2018

Sheets of human retinal progenitor transplants improve vision in rats with severe retinal degeneration.

Bin Lin, Bryce T McLelland, Anuradha Mathur, Robert B Aramant, Magdalene J Seiler

Abstract read
In one paragraph

Article in Experimental eye research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Review
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  5. Animal models for the evaluation of retinal stem cell therapies.Progress in retinal and eye research · 2025
    Review
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  7. Article
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  9. Review
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  12. Review
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  14. Review
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  17. Retinal Organoid Technology: Where Are We Now?International journal of molecular sciences · 2021
    Review
  18. Article
  19. Article
  20. 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

5 authors.

Bin LinStem Cell Research Center, University of CalifoArnia, Irvine, United States.
Bryce T McLellandStem Cell Research Center, University of CalifoArnia, Irvine, United States.
Anuradha MathurStem Cell Research Center, University of CalifoArnia, Irvine, United States.
Robert B AramantStem Cell Research Center, University of CalifoArnia, Irvine, United States.
Magdalene J SeilerStem Cell Research Center, University of CalifoArnia, Irvine, United States; Department of Physical Medicine & Rehabilitation, University of California, Irvine, United States. Electronic address: mseiler@uci.edu.

Funding

3D retina-RPE constructs for vision restoration in new retinal degeneration mR01EY024045 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KEIRSTEAD, HANS S · 2014 to 2016
$1.0M
NEI NIH HHS R01 EY024045
6 · The paper itself

Abstract

Loss of photoreceptors and other retinal cells is a common endpoint in retinal degenerate (RD) diseases that cause blindness. Retinal transplantation is a potential therapy to replace damaged retinal cells and improve vision. In this study, we examined the development of human fetal retinal sheets with or without their retinal pigment epithelium (RPE) transplanted to immunodeficient retinal degenerate rho S334ter-3 rats. Sheets were dissected from fetal human eyes (11-15.7 weeks gestation) and then transplanted to the subretinal space of 24-31 d old RD nude rats. Every month post surgery, eyes were imaged by high-resolution spectral-domain optical coherence tomography (SD-OCT). SD-OCT showed that transplants were placed into the subretinal space and developed laminated areas or rosettes, with clear development of plexiform layers first seen in OCT at 3 months post surgery. Several months later, as could be expected by the much slower development of human cells compared to rat cells, transplant photoreceptors developed inner and later outer segments. Retinal sections were analyzed by immunohistochemistry for human and retinal markers and confirmed the formation of several retinal subtypes within the retinal layers. Transplant cells extended processes and a lot of the cells could also be seen migrating into the host retina. At 5.8-8.6 months post surgery, selected rats were exposed to light flashes and recorded for visual responses in superior colliculus, (visual center in midbrain). Four of seven rats with transplants showed responses to flashes of light in a limited area of superior colliculus. No response with the same dim light intensity was found in age-matched RD controls (non-surgery or sham surgery). In summary, our data showed that human fetal retinal sheets transplanted to the severely disturbed subretinal space of RD nude rats develop mature photoreceptors and other retinal cells, integrate with the host and induce vision improvement.

Indexed as

RetinaAnimalsBiomarkersHumansMicrogliaNeurogliaPhotoreceptor CellsRatsRetinal DegenerationStem Cell TransplantationSuperior ColliculiTomography, Optical CoherenceVision, OcularBiomarkersElectrophysiologyImmunodeficient ratOptical coherence tomographyRetinal developmentRetinal restorationRetinal transplantationStem cellsSuperior colliculus recording

Identifiers

PMID29782826
PMCPMC6110982

What Socratic holds

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LicenceTDM
Read underepoch 390

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 Socratic graph.