Evidence map›Paper›PMID 35330684›Full record

ArticleiScience2022

One-step induction of photoreceptor-like cells from human iPSCs by delivering transcription factors.

Yuki Otsuka, Keiko Imamura, Akio Oishi, Takayuki Kondo, Mika Suga, Yuichiro Yada, Ran Shibukawa, Yasue Okanishi, Yukako Sagara, Kayoko Tsukita and 2 more

Abstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Restoring Sight: The Journey of AIPL1 from Discovery to Therapy.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. 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

12 authors.

Yuki OtsukaiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Keiko ImamuraiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Akio OishiDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Takayuki KondoiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Mika SugaiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Yuichiro YadaiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Ran ShibukawaiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Yasue OkanishiiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Yukako SagaraiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Kayoko TsukitaiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.
Akitaka TsujikawaDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Haruhisa InoueiPSC-based Drug Discovery and Development Team, RIKEN BioResource Research Center, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal dystrophies (RDs) lead to irreversible vision impairment with no radical treatment. Although photoreceptor cells (PRCs) differentiated from human induced pluripotent stem cells (iPSCs) are essential for the study of RDs as a scalable source, current differentiation methods for PRCs require multiple steps. To address these issues, we developed a method to generate PRCs from human iPSCs by introducing the transcription factors, CRX and NEUROD1. This approach enabled us to generate induced photoreceptor-like cells (iPRCs) expressing PRC markers. Single-cell RNA sequencing revealed the transcriptome of iPRCs in which the genes associated with phototransduction were expressed. Generated iPRCs exhibited their functional properties in calcium imaging. Furthermore, light-induced damage on iPRCs was inhibited by an antioxidant compound. This simple approach would facilitate the availability of materials for PRC-related research and provide a useful application for disease modeling and drug discovery.

Indexed as

Cell biologyMolecular biologyStem cells research

Identifiers

PMID35330684
PMCPMC8938283

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.