Evidence map›Paper›PMID 23495178›Full record

ArticleStem cells (Dayton, Ohio)2013

Developing rods transplanted into the degenerating retina of Crx-knockout mice exhibit neural activity similar to native photoreceptors.

Kohei Homma, Satoshi Okamoto, Michiko Mandai, Norimoto Gotoh, Harsha K Rajasimha, Yi-Sheng Chang, Shan Chen, Wei Li, Tiziana Cogliati, Anand Swaroop and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Cone Rod Homeobox (Ophthalmic genetics · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Genome Editing in Patient iPSCs Corrects the Most PrevalentMolecular therapy. Methods & clinical development · 2020
    Article
  16. Article
  17. Retinal stem cell transplantation: Balancing safety and potential.Progress in retinal and eye research · 2020
    Review
  18. Review
  19. Review
  20. 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

11 authors at 4 institutions in 3 countries.

Kohei HommaLaboratory for Retinal Regeneration, Center for Developmental Biology, RIKEN, Kobe, Japan. kohei.homma@nih.gov
Satoshi Okamoto
Michiko Mandai
Norimoto Gotoh
Harsha K Rajasimha
Yi-Sheng Chang
Shan Chen
Wei Li
Tiziana Cogliati
Anand Swaroop
Masayo Takahashi
National Eye Institute · USRIKEN Center for Biosystems Dynamics Research · JPNational Cheng Kung University Hospital · TWNational Institutes of Health · US

Funding

Interventional approaches for restoring visionZIAEY000474 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2019
$15.5M
Intramural NIH HHS Z99 EY999999Intramural NIH HHS ZIA EY000474
6 · The paper itself

Abstract

Replacement of dysfunctional or dying photoreceptors offers a promising approach for retinal neurodegenerative diseases, including age-related macular degeneration and retinitis pigmentosa. Several studies have demonstrated the integration and differentiation of developing rod photoreceptors when transplanted in wild-type or degenerating retina; however, the physiology and function of the donor cells are not adequately defined. Here, we describe the physiological properties of developing rod photoreceptors that are tagged with green fluorescent protein (GFP) driven by the promoter of rod differentiation factor, Nrl. GFP-tagged developing rods show Ca(2 +) responses and rectifier outward currents that are smaller than those observed in fully developed photoreceptors, suggesting their immature developmental state. These immature rods also exhibit hyperpolarization-activated current (Ih ) induced by the activation of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels. When transplanted into the subretinal space of wild-type or retinal degeneration mice, GFP-tagged developing rods can integrate into the photoreceptor outer nuclear layer in wild-type mouse retina and exhibit Ca(2 +) responses and membrane current comparable to native rod photoreceptors. A proportion of grafted rods develop rhodopsin-positive outer segment-like structures within 2 weeks after transplantation into the retina of Crx-knockout mice and produce rectifier outward current and Ih upon membrane depolarization and hyperpolarization. GFP-positive rods derived from induced pluripotent stem (iPS) cells also display similar membrane current Ih as native developing rod photoreceptors, express rod-specific phototransduction genes, and HCN-1 channels. We conclude that Nrl-promoter-driven GFP-tagged donor photoreceptors exhibit physiological characteristics of rods and that iPS cell-derived rods in vitro may provide a renewable source for cell-replacement therapy.

Indexed as

AnimalsBasic-Leucine Zipper Transcription FactorsCalciumCell DifferentiationCells, CulturedEye ProteinsGreen Fluorescent ProteinsHomeodomain ProteinsHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsInduced Pluripotent Stem CellsMembrane PotentialsMiceMice, Inbred C57BLMice, KnockoutPhotoreceptor Cells, VertebratePromoter Regions, GeneticBasic-Leucine Zipper Transcription FactorsCalciumcone rod homeobox proteinEye ProteinsGreen Fluorescent ProteinsHomeodomain ProteinsHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsNrl protein, mouseTrans-Activators

Identifiers

PMID23495178
PMCPMC4540234
OpenAlexW1983504539

What OpenQuestion holds

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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.