Evidence map›Paper›PMID 30210491›Full record

ArticleFrontiers in immunology2018

GM-CSF Quantity Has a Selective Effect on Granulocytic vs. Monocytic Myeloid Development and Function.

Li Sun, Jai Rautela, Rebecca B Delconte, Fernando Souza-Fonseca-Guimaraes, Emma M Carrington, Robyn L Schenk, Marco J Herold, Nicholas D Huntington, Andrew M Lew, Yuekang Xu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. GM-CSF Promotes Superior In Vitro Differentiation of MHC IIInternational journal of molecular sciences · 2026
    Article
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  6. Review
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  9. Roles of macrophages in lupus nephritis.Frontiers in pharmacology · 2024
    Review
  10. Article
  11. Article
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  14. Article
  15. Repositioning TNature immunology · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. GM-CSF in inflammation.The Journal of experimental medicine · 2020
    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

11 authors at 3 institutions in 2 countries.

Li SunAnhui Provincial Key Laboratory for Conservation and Exploitation of Biological Resources, School of Life Science, Anhui Normal University, Wuhu, China.
Jai RautelaThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Rebecca B DelconteThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Fernando Souza-Fonseca-GuimaraesThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Emma M CarringtonThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Robyn L SchenkThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Marco J HeroldThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Nicholas D HuntingtonThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Andrew M LewThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Yuekang XuAnhui Provincial Key Laboratory for Conservation and Exploitation of Biological Resources, School of Life Science, Anhui Normal University, Wuhu, China.
Yifan ZhanThe Walter & Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Walter and Eliza Hall Institute of Medical Research · AUUniversity of Melbourne · AUAnhui Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GM-CSF promotes myeloid differentiation of cultured bone marrow cells into cells of the granulocytic and monocytic lineage; the latter can further differentiate into monocytes/macrophages and dendritic cells. How GM-CSF selects for these different myeloid fates is unresolved. GM-CSF levels can change either iatrogenically (e.g., augmenting leukopoiesis after radiotherapy) or naturally (e.g., during infection or inflammation) resulting in different immunological outcomes. Therefore, we asked whether the dose of GM-CSF may regulate the development of three types of myeloid cells. Here, we showed that GM-CSF acted as a molecular rheostat where the quantity determined which cell type was favored; moreover, the cellular process by which this was achieved was different for each cell type. Thus, low quantities of GM-CSF promoted the granulocytic lineage, mainly through survival. High quantities promoted the monocytic lineage, mainly through proliferation, whereas moderate quantities promoted moDCs, mainly through differentiation. Finally, we demonstrated that monocytes/macrophages generated with different doses of GM-CSF differed in function. We contend that this selective effect of GM-CSF dose on myeloid differentiation and function should be taken into consideration during pathophysiological states that may alter GM-CSF levels and during GM-CSF agonistic or antagonistic therapy.

Indexed as

AnimalsCell DifferentiationDose-Response Relationship, DrugGranulocyte-Macrophage Colony-Stimulating FactorGranulocytesMacrophagesMiceMice, KnockoutMonocytesGranulocyte-Macrophage Colony-Stimulating Factorcytokinesdendritic cellsGM-CSFgranulocytesinflammation mediators

Identifiers

PMID30210491
PMCPMC6120981
OpenAlexW2889203430

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.