Evidence map›Paper›PMID 28191760›Full record

ArticleStem cells translational medicine2017

Directing Differentiation of Pluripotent Stem Cells Toward Retinal Pigment Epithelium Lineage.

Parul Choudhary, Heather Booth, Alex Gutteridge, Beata Surmacz, Irene Louca, Juliette Steer, Julie Kerby, Paul John Whiting

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 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
3.1field-weighted citation impact, top 8% 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, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Molecular and cellular imaging of the eye.Biomedical optics express · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Chromosome 10q26-driven age-related macular degeneration is associated with reduced levels ofProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Delivery Systems of Retinoprotective Proteins in the Retina.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

8 authors at 1 institution in 1 country.

Parul ChoudharyPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Heather BoothPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Alex GutteridgePfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Beata SurmaczPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Irene LoucaPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Juliette SteerPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Julie KerbyPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Paul John WhitingPfizer Neuroscience and Pain Research Unit, Great Abington, Cambridge, United Kingdom.
Pfizer (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of efficient and reproducible conditions for directed differentiation of pluripotent stem cells into specific cell types is important not only to understand early human development but also to enable more practical applications, such as in vitro disease modeling, drug discovery, and cell therapies. The differentiation of stem cells to retinal pigment epithelium (RPE) in particular holds promise as a source of cells for therapeutic replacement in age-related macular degeneration. Here we show development of an efficient method for deriving homogeneous RPE populations in a period of 45 days using an adherent, monolayer system and defined xeno-free media and matrices. The method utilizes sequential inhibition and activation of the Activin and bone morphogenetic protein signaling pathways and can be applied to both human embryonic stem cells and induced pluripotent stem cells as the starting population. In addition, we use whole genome transcript analysis to characterize cells at different stages of differentiation that provides further understanding of the developmental dynamics and fate specification of RPE. We show that with the described method, RPE develop through stages consistent with their formation during embryonic development. This characterization- together with the absence of steps involving embryoid bodies, three-dimensional culture, or manual dissections, which are common features of other protocols-makes this process very attractive for use in research as well as for clinical applications. Stem Cells Translational Medicine 2017;6:490-501.

Indexed as

Cell DifferentiationCell LineageCellular ReprogrammingCellular Reprogramming TechniquesActivinsBone Morphogenetic ProteinsCells, CulturedEpithelial CellsGene Expression Regulation, DevelopmentalHumansInduced Pluripotent Stem CellsPhenotypePyrazolesPyrimidinesRetinal Pigment EpitheliumSignal TransductionActivinsBone Morphogenetic ProteinsLDN 193189PyrazolesPyrimidinesActivinBone morphogenetic proteinDirected differentiationRetinal pigment epitheliumStem cells

Identifiers

PMID28191760
PMCPMC5442825
OpenAlexW2515336799

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.