Evidence map›Paper›PMID 36878908›Full record

ArticleNature communications2023

Zebrafish pigment cells develop directly from persistent highly multipotent progenitors.

Tatiana Subkhankulova, Karen Camargo Sosa, Leonid A Uroshlev, Masataka Nikaido, Noah Shriever, Artem S Kasianov, Xueyan Yang, Frederico S L M Rodrigues, Thomas J Carney, Gemma Bavister and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. 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
9.8field-weighted citation impact, top 1% 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, 70 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Control Strategies in Guanine Biocrystallization.Angewandte Chemie (International ed. in English) · 2026
    Review
  5. Lysosome-related organelles orchestrate guanine crystal formation in pigment cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Linking tissue morphology and tissue healing in a cell-fate model.Frontiers in cell and developmental biology · 2026
    Article
  9. Article
  10. Article
  11. Specialized molecular pathways drive the formation of light-scattering assemblies in leucophores.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. High frequency of melanoma inTheranostics · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Genes · 2023
    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

15 authors at 7 institutions in 5 countries.

Tatiana Subkhankulova *Department of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Karen Camargo Sosa *Department of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID 0000-0002-9803-6372
Leonid A UroshlevVavilov Institute of General Genetics, Russian Academy of Sciences, Ul. Gubkina 3, Moscow, 119991, Russia.ORCID 0000-0003-2878-5703
Masataka NikaidoDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Noah ShrieverDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID 0000-0002-9718-359X
Artem S KasianovVavilov Institute of General Genetics, Russian Academy of Sciences, Ul. Gubkina 3, Moscow, 119991, Russia.ORCID 0000-0001-8086-392X
Xueyan YangDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Frederico S L M RodriguesDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID 0000-0001-8458-184X
Thomas J CarneyDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID 0000-0003-2371-1924
Gemma BavisterDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Hartmut SchwetlickDepartment of Mathematical Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Jonathan H P DawesDepartment of Mathematical Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID 0000-0002-4347-9985
Andrea RoccoDepartment of Microbial Sciences, FHMS, University of Surrey, GU2 7XH, Guildford, UK.ORCID 0000-0002-0974-5522
Vsevolod J MakeevVavilov Institute of General Genetics, Russian Academy of Sciences, Ul. Gubkina 3, Moscow, 119991, Russia.ORCID 0000-0001-9405-9748
Robert N KelshDepartment of Life Sciences, University of Bath, Claverton Down, Bath, BA2 7AY, UK. bssrnk@bath.ac.uk.ORCID 0000-0002-9381-0066
University of Bath · GBMoscow Institute of Physics and Technology · RUFudan University · CNNanyang Technological University · SGUniversity of Hyogo · JPUniversity of Surrey · GBVavilov Institute of General Genetics · RU

Funding

Biotechnology and Biological Sciences Research Council BB/ L00769X/1Biotechnology and Biological Sciences Research Council BB/L007789/1Biotechnology and Biological Sciences Research Council BB/S015906/1Biotechnology and Biological Sciences Research Council BB/S01604X/1Wellcome Trust
6 · The paper itself

Abstract

Neural crest cells are highly multipotent stem cells, but it remains unclear how their fate restriction to specific fates occurs. The direct fate restriction model hypothesises that migrating cells maintain full multipotency, whilst progressive fate restriction envisages fully multipotent cells transitioning to partially-restricted intermediates before committing to individual fates. Using zebrafish pigment cell development as a model, we show applying NanoString hybridization single cell transcriptional profiling and RNAscope in situ hybridization that neural crest cells retain broad multipotency throughout migration and even in post-migratory cells in vivo, with no evidence for partially-restricted intermediates. We find that leukocyte tyrosine kinase early expression marks a multipotent stage, with signalling driving iridophore differentiation through repression of fate-specific transcription factors for other fates. We reconcile the direct and progressive fate restriction models by proposing that pigment cell development occurs directly, but dynamically, from a highly multipotent state, consistent with our recently-proposed Cyclical Fate Restriction model.

Indexed as

Automobile DrivingZebrafishAnimalsCell DifferentiationHematopoietic Stem CellsMultipotent Stem Cells

Identifiers

PMID36878908
PMCPMC9988989
OpenAlexW4323310465

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.