Evidence map›Paper›PMID 40387575›Full record

ArticleDevelopment (Cambridge, England)2025

CSF1R ligands promote microglial proliferation but are not the sole regulators of developmental microglial proliferation.

Brady P Hammond, Sameera Zia, Eugene Hahn, Margarita Kapustina, Tristan Lange, Sarah Friesen, Rupali Manek, Kelly V Lee, Adrian Castellanos-Molina, Floriane Bretheau and 4 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Brady P HammondNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Sameera ZiaNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Eugene HahnNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Margarita KapustinaDepartment of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, V6T 1Z3, Canada.
Tristan LangeNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Sarah FriesenNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Rupali ManekNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Kelly V LeeNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Adrian Castellanos-MolinaAxe Neurosciences du Centre de Recherche du Centre hospitalier universitaire (CHU) de Québec, Université Laval, Québec City, G1V 0E8, Canada.
Floriane BretheauAxe Neurosciences du Centre de Recherche du Centre hospitalier universitaire (CHU) de Québec, Université Laval, Québec City, G1V 0E8, Canada.
Mark S CembrowskiDepartment of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, V6T 1Z3, Canada.
Bradley J KerrNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.
Steve LacroixAxe Neurosciences du Centre de Recherche du Centre hospitalier universitaire (CHU) de Québec, Université Laval, Québec City, G1V 0E8, Canada.
Jason R PlemelNeuroscience and Mental Health Institute, University of Alberta, Edmonton, T6G 2R3, Canada.ORCID 0000-0003-1385-1464

Funding

Canada Research ChairsNatural Sciences and Engineering Research Council of Canada RGPIN-2019-04533University of Alberta
6 · The paper itself

Abstract

Microglia - the predominant immune cells of the brain and spinal cord - perform essential functions for the development and maintenance of the central nervous system, contingent upon the regulated developmental proliferation of microglia. However, the factor(s) that regulate microglial proliferation remain unclear. Here, we confirmed the timeline of developmental proliferation and used bioinformatics to identify potential signalling onto microglia in mouse from datasets collected at an age of high developmental microglial proliferation. Of the predicted factors, we found that colony stimulating factor 1 receptor (CSF1R) ligands boosted proliferation in vitro and were increasingly expressed in the brain across development with each displaying a distinct regional and temporal expression pattern. However, we did not observe a coincident alteration to CSF1R ligand levels in a model of abnormal developmental proliferation. Together, although CSF1R ligands can promote microglial proliferation in culture, their developmental expression patterns suggest that they function alongside other unknown factors to regulate developmental microglial proliferation.

Indexed as

Cell ProliferationMicrogliaReceptors, Granulocyte-Macrophage Colony-Stimulating FactorAnimalsBrainGene Expression Regulation, DevelopmentalLigandsMiceMice, Inbred C57BLSignal TransductionCsf1r protein, mouseLigandsReceptors, Granulocyte-Macrophage Colony-Stimulating FactorBrainCSF1CSF1RDevelopmentIL34MicrogliaMouseProliferation

Identifiers

PMID40387575
PMCPMC12188242

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.