Evidence map›Paper›PMID 31857239›Full record

ArticleCellular signalling2020

Divergent effects of Wnt5b on IL-3- and GM-CSF-induced myeloid differentiation.

Marina Mastelaro de Rezende, John-Poul Ng-Blichfeldt, Giselle Zenker Justo, Edgar Julian Paredes-Gamero, Reinoud Gosens

Open access · hybridAbstract read
In one paragraph

Article in Cellular signalling, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. WNT5B in Physiology and Disease.Frontiers in cell and developmental biology · 2021
    Review
  8. 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

5 authors at 3 institutions in 3 countries.

Marina Mastelaro de RezendeDepartamento de Bioquímica, Universidade Federal de São Paulo (UNIFESP), São Paulo 04044-020, Brazil; Department of Molecular Pharmacology, University of Groningen, Groningen 9713AV, Netherlands.
John-Poul Ng-BlichfeldtDepartment of Molecular Pharmacology, University of Groningen, Groningen 9713AV, Netherlands; MRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.
Giselle Zenker JustoDepartamento de Bioquímica, Universidade Federal de São Paulo (UNIFESP), São Paulo 04044-020, Brazil; Departamento de Ciências Farmacêuticas, Universidade Federal de São Paulo (UNIFESP), Diadema 09913-030, Brazil.
Edgar Julian Paredes-GameroDepartamento de Bioquímica, Universidade Federal de São Paulo (UNIFESP), São Paulo 04044-020, Brazil; Faculdade de Ciências Farmacêuticas, Alimentos e Nutrição, Universidade Federal de Mato Grosso do Sul, 79070-900, Campo Grande, Mato Grosso do Sul, Brazil.
Reinoud GosensDepartment of Molecular Pharmacology, University of Groningen, Groningen 9713AV, Netherlands. Electronic address: r.gosens@rug.nl.
University of Groningen · NLUniversidade Federal de Mato Grosso do Sul · BRUniversidade Federal de São Paulo · BR

Funding

Medical Research Council MC_UP_1201/11
6 · The paper itself

Abstract

The multiple specialized cell types of the hematopoietic system originate from differentiation of hematopoietic stem cells and progenitors (HSPC), which can generate both lymphoid and myeloid lineages. The myeloid lineage is preferentially maintained during ageing, but the mechanisms that contribute to this process are incompletely understood. Here, we studied the roles of Wnt5a and Wnt5b, ligands that have previously been linked to hematopoietic stem cell ageing and that are abundantly expressed by both hematopoietic progenitors and bone-marrow derived niche cells. Whereas Wnt5a had no major effects on primitive cell differentiation, Wnt5b had profound and divergent effects on cytokine-induced myeloid differentiation. Remarkably, while IL-3-mediated myeloid differentiation was largely repressed by Wnt5b, GM-CSF-induced myeloid differentiation was augmented. Furthermore, in the presence of IL-3, Wnt5b enhanced HSPC self-renewal, whereas in the presence of GM-CSF, Wnt5b accelerated differentiation, leading to progenitor cell exhaustion. Our results highlight discrepancies between IL-3 and GM-CSF, and reveal novel effects of Wnt5b on the hematopoietic system.

Indexed as

AnimalsCell DifferentiationGranulocyte-Macrophage Colony-Stimulating FactorInterleukin-3Mice, Inbred C57BLMyeloid CellsStem CellsWnt ProteinsGranulocyte-Macrophage Colony-Stimulating FactorInterleukin-3Wnt ProteinsCytokinesDifferentiationMyelopoiesisWnt5bWnt ligands

Identifiers

PMID31857239
PMCPMC7116107
OpenAlexW2994770891

What OpenQuestion holds

Textmetadata
LicenceTDM
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.