Evidence map›Paper›PMID 37479765›Full record

ArticleCommunications biology2023

Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells.

Sandy Gozlan, Vivien Batoumeni, Tara Fournier, Céline Nanteau, Anais Potey, Marilou Clémençon, Gaël Orieux, José-Alain Sahel, Olivier Goureau, Jérôme E Roger and 1 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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 1 institution in 2 countries.

Sandy GozlanSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
Vivien BatoumeniSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
Tara FournierSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.ORCID 0009-0006-7708-9033
Céline NanteauSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
Anais PoteySorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
Marilou ClémençonSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.ORCID 0000-0003-1719-449X
Gaël OrieuxSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
José-Alain SahelSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
Olivier GoureauSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France.
Jérôme E RogerParis-Saclay Institute of Neuroscience, CERTO-Retina France, CNRS, Université Paris-Saclay, 91400, Saclay, France.ORCID 0000-0002-5061-230X
Sacha ReichmanSorbonne Université, INSERM, CNRS, Institut de la Vision, F-75012, Paris, France. sacha.reichman@inserm.fr.ORCID 0000-0003-1776-6339
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal progenitor cells (RPCs) are the source of all retinal cell types during retinogenesis. Until now, the isolation and expansion of RPCs has been at the expense of their multipotency. Here, we report simple methods and media for the generation, expansion, and cryopreservation of human induced pluripotent stem-cell derived-RPCs (hiRPCs). Thawed and passed hiRPCs maintained biochemical and transcriptional RPC phenotypes and their ability to differentiate into all retinal cell types. Specific conditions allowed the generation of large cultures of photoreceptor precursors enriched up to 90% within a few weeks and without a purification step. Combined RNA-seq analysis between hiRPCs and retinal organoids identified genes involved in developmental or degenerative retinal diseases. Thus, hiRPC lines could provide a valuable source of retinal cells for cell-based therapies or drug discovery and could be an advanced cellular tool to better understand retinal dystrophies.

Indexed as

Induced Pluripotent Stem CellsRetinal DiseasesCollagen DiseasesHumansNeuronsRetinaSkin Diseases, Genetic

Identifiers

PMID37479765
PMCPMC10362027
OpenAlexW4385064594

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.