Evidence map›Paper›PMID 28790106›Full record

ArticleBlood2017

KIT signaling is dispensable for human mast cell progenitor development.

Joakim S Dahlin, Maria Ekoff, Jennine Grootens, Liza Löf, Rose-Marie Amini, Hans Hagberg, Johanna S Ungerstedt, Ulla Olsson-Strömberg, Gunnar Nilsson

Abstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Hematopoiesis and Mast Cell Development.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Mast Cells in Upper and Lower Airway Diseases: Sentinels in the Front Line.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Human Lung Mast Cells: Therapeutic Implications in Asthma.International journal of molecular sciences · 2022
    Review
  17. Article
  18. KIT as a master regulator of the mast cell lineage.The Journal of allergy and clinical immunology · 2022
    Review
  19. UVB-Induced Secretion of IL-1BioMed research international · 2022
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Joakim S DahlinDepartment of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Maria EkoffDepartment of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Jennine GrootensDepartment of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Liza LöfDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, and.
Rose-Marie AminiDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Hans HagbergDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Johanna S UngerstedtDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Ulla Olsson-StrömbergDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden; and.
Gunnar NilssonDepartment of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human hematopoietic progenitors are generally assumed to require stem cell factor (SCF) and KIT signaling during differentiation for the formation of mast cells. Imatinib treatment, which inhibits KIT signaling, depletes mast cells in vivo. Furthermore, the absence of SCF or imatinib treatment prevents progenitors from developing into mast cells in vitro. However, these observations do not mean that mast cell progenitors require SCF and KIT signaling throughout differentiation. Here, we demonstrate that circulating mast cell progenitors are present in patients undergoing imatinib treatment. In addition, we show that mast cell progenitors from peripheral blood survive, mature, and proliferate without SCF and KIT signaling in vitro. Contrary to the prevailing consensus, our results show that SCF and KIT signaling are dispensable for early mast cell development.

Indexed as

Cell DifferentiationCell ProliferationCase-Control StudiesCells, CulturedCell SurvivalHumansImatinib MesylateMast CellsProto-Oncogene Proteins c-kitSignal TransductionStem CellsImatinib MesylateProto-Oncogene Proteins c-kit

Identifiers

PMID28790106
PMCPMC5659818

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.