Evidence map›Paper›PMID 29758105›Full record

ArticleJournal of leukocyte biology2018

Transcriptional profiling of eosinophil subsets in interleukin-5 transgenic mice.

Kirsten A Fairfax, Jessica E Bolden, Aaron J Robinson, Erin C Lucas, Tracey M Baldwin, Kerry A Ramsay, Rebecca Cole, Douglas J Hilton, Carolyn A de Graaf

Open access · hybridAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Defining mesenchymal stem/stromal cell-induced myeloid-derived suppressor cells using single-cell transcriptomics.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  5. Article
  6. The diversity of neuroimmune circuits controlling lung inflammation.American journal of physiology. Lung cellular and molecular physiology · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

9 authors at 2 institutions in 1 country.

Kirsten A FairfaxDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Jessica E BoldenDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Aaron J RobinsonDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Erin C LucasDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Tracey M BaldwinDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Kerry A RamsayDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Rebecca ColeDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Douglas J HiltonDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Carolyn A de GraafDivision of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Walter and Eliza Hall Institute of Medical Research · AUUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophils are important in fighting parasitic infections and are implicated in the pathogenesis of asthma and allergy. IL-5 is a critical regulator of eosinophil development, controlling proliferation, differentiation, and maturation of the lineage. Mice that constitutively express IL-5 have in excess of 10-fold more eosinophils in the hematopoietic organs than their wild type (WT) counterparts. We have identified that much of this expansion is in a population of Siglec-F high eosinophils, which are rare in WT mice. In this study, we assessed transcription in myeloid progenitors, eosinophil precursors, and Siglec-F medium and Siglec-F high eosinophils from IL-5 transgenic mice and in doing so have created a useful resource for eosinophil biologists. We have then utilized these populations to construct an eosinophil trajectory based on gene expression and to identify gene sets that are associated with eosinophil lineage progression. Cell cycle genes were significantly associated with the trajectory, and we experimentally demonstrate an increasing trend toward quiescence along the trajectory. Additionally, we found gene expression changes associated with constitutive IL-5 signaling in eosinophil progenitors, many of which were not observed in eosinophils.

Indexed as

Gene Expression ProfilingAnimalsCell DifferentiationCell LineageEosinophilsInterleukin-5MiceMice, TransgenicMyeloid Progenitor CellsInterleukin-5gene expressiongranulocyteprogenitorSiglec-Ftrajectory

Identifiers

PMID29758105
PMCPMC6749942
OpenAlexW2804882087

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.