Evidence map›Paper›PMID 21771814›Full record

ArticleDevelopment (Cambridge, England)2011

Differentiated melanocyte cell division occurs in vivo and is promoted by mutations in Mitf.

Kerrie L Taylor, James A Lister, Zhiqiang Zeng, Hironori Ishizaki, Caroline Anderson, Robert N Kelsh, Ian J Jackson, E Elizabeth Patton

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

34 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Telomere Checkpoint in Development and Aging.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. MITF-the first 25 years.Genes & development · 2019
    Review
  18. Review
  19. Article
  20. Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer.International journal of molecular sciences · 2017
    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.

Kerrie L TaylorMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, Crewe Road South, Edinburgh EH4 2XR, UK.
James A Lister
Zhiqiang Zeng
Hironori Ishizaki
Caroline Anderson
Robert N Kelsh
Ian J Jackson
E Elizabeth Patton
Edinburgh Cancer Research · GB

Funding

Medical Research Council G120/875Medical Research Council MC_PC_U127527200Medical Research Council MC_PC_U127585840Medical Research Council MC_U127527200Medical Research Council MC_U127585840Wellcome Trust
6 · The paper itself

Abstract

Coordination of cell proliferation and differentiation is crucial for tissue formation, repair and regeneration. Some tissues, such as skin and blood, depend on differentiation of a pluripotent stem cell population, whereas others depend on the division of differentiated cells. In development and in the hair follicle, pigmented melanocytes are derived from undifferentiated precursor cells or stem cells. However, differentiated melanocytes may also have proliferative capacity in animals, and the potential for differentiated melanocyte cell division in development and regeneration remains largely unexplored. Here, we use time-lapse imaging of the developing zebrafish to show that while most melanocytes arise from undifferentiated precursor cells, an unexpected subpopulation of differentiated melanocytes arises by cell division. Depletion of the overall melanocyte population triggers a regeneration phase in which differentiated melanocyte division is significantly enhanced, particularly in young differentiated melanocytes. Additionally, we find reduced levels of Mitf activity using an mitfa temperature-sensitive line results in a dramatic increase in differentiated melanocyte cell division. This supports models that in addition to promoting differentiation, Mitf also promotes withdrawal from the cell cycle. We suggest differentiated cell division is relevant to melanoma progression because the human melanoma mutation MITF(4T)(Δ)(2B) promotes increased and serial differentiated melanocyte division in zebrafish. These results reveal a novel pathway of differentiated melanocyte division in vivo, and that Mitf activity is essential for maintaining cell cycle arrest in differentiated melanocytes.

Indexed as

Cell DivisionMutationAnimalsCell DifferentiationGene Expression Regulation, DevelopmentalHumansMelanocytesMicrophthalmia-Associated Transcription FactorZebrafishZebrafish ProteinsMicrophthalmia-Associated Transcription Factormitfa protein, zebrafishMITF protein, humanZebrafish Proteins

Identifiers

PMID21771814
PMCPMC3143570
OpenAlexW2132314043

What OpenQuestion holds

Textmetadata
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.