Evidence map›Paper›PMID 31373067›Full record

ReviewThe EMBO journal2019

Microglial subtypes: diversity within the microglial community.

Vassilis Stratoulias, Jose Luis Venero, Marie-Ève Tremblay, Bertrand Joseph

Open access · hybridAbstract readReview
In one paragraph

Review in The EMBO journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 330 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
330citing papers in PubMed, 2 pooled it
31.9field-weighted citation impact, top 1% 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

330 citing papers in PubMed, 2 syntheses or guidelines pooled it, 558 citations in OpenAlex.

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  10. Human IL-34 Deficiency Primes Microglia Toward Alzheimer's Disease-Associated States.medRxiv : the preprint server for health sciences · 2026
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270 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 3 countries.

Vassilis StratouliasToxicology Unit, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-9724-6589
Jose Luis VeneroDepartamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad de Sevilla, Sevilla, Spain.
Marie-Ève TremblayDepartment of Molecular Medicine, Université Laval, Quebec, QC, Canada.
Bertrand JosephToxicology Unit, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-5655-9979
Karolinska Institutet · SEInstituto de Biomedicina de Sevilla · ESUniversité Laval · CA

Funding

Barncancerfonden (Swedish Childhood Cancer Foundation)Canada Research Chair (Tier 2) of Neuroimmune Plasticity in Health and TherapyCancerfonden (Swedish Cancer Society)Hjärnfonden (Swedish Brain Foundation)Karolinska Institutet FoundationSigrid Juséliuksen Säätiö (Sigrid Jusélius Stiftelse)Spanish Ministerio de Ciencia, Innovación y Universidades FEDER/UE RTI2018-098645-B-100Swedish Cancer FoundationSwedish Research CouncilTracInflam grant from ERA-NET NEURON Neuroinflammation
6 · The paper itself

Abstract

Microglia are brain-resident macrophages forming the first active immune barrier in the central nervous system. They fulfill multiple functions across development and adulthood and under disease conditions. Current understanding revolves around microglia acquiring distinct phenotypes upon exposure to extrinsic cues in their environment. However, emerging evidence suggests that microglia display differences in their functions that are not exclusively driven by their milieu, rather by the unique properties these cells possess. This microglial intrinsic heterogeneity has been largely overlooked, favoring the prevailing view that microglia are a single-cell type endowed with spectacular plasticity, allowing them to acquire multiple phenotypes and thereby fulfill their numerous functions in health and disease. Here, we review the evidence that microglia might form a community of cells in which each member (or "subtype") displays intrinsic properties and performs unique functions. Distinctive features and functional implications of several microglial subtypes are considered, across contexts of health and disease. Finally, we suggest that microglial subtype categorization shall be based on function and we propose ways for studying them. Hence, we advocate that plasticity (reaction states) and diversity (subtypes) should both be considered when studying the multitasking microglia.

Indexed as

AnimalsCell PlasticityHumansMicrogliaPhenotypediseaseheterogeneityhomeostasismicrogliasubtypes

Identifiers

PMID31373067
PMCPMC6717890
OpenAlexW2965025337

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.